HOUSE DUST injection, solution ALMOND- almond food injection, solution APPLE- apple food injection, solution APRICOT injection, solution ASPARAGUS injection, solution AVOCADO injection, solution BANANA injection, solution BARLEY (barley food .......> FRAXINUS VELUTINA POLLEN (arizona ash) injection, solution AMARANTHUS RETROFLEXUS POLLEN (rough pigweed redroot) injection, solution LIQUIDAMBAR STYRACIFLUA POLLEN (sweetgum non stock) injection, solution JUGLANS NIGRA POLLEN (walnut black pollen) injection, solution SALIX NIGRA POLLEN- black willow injection, solution [ALK-Abello, Inc.] FRAXINUS VELUTINA POLLEN- arizona ash injection, solution AMARANTHUS RETROFLEXUS POLLEN- rough pigweed redroot injection, solution LIQUIDAMBAR STYRACIFLUA POLLEN- sweetgum non stock injection, solution JUGLANS NIGRA POLLEN- walnut black pollen injection, solution SALIX NIGRA POLLEN- black willow injection, solution

SALIX NIGRA POLLEN by

Drug Labeling and Warnings

SALIX NIGRA POLLEN by is a Other medication manufactured, distributed, or labeled by ALK-Abello, Inc., Alk-abello, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

ALLERGENIC EXTRACTS,

FOR DIAGNOSTIC USE ONLY

DIRECTIONS FOR USE

BOXED WARNING

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WARNING

This product is intended for use by physicians who are experienced in the administration of allergenic extracts and the emergency care of anaphylaxis, or for use under the guidance of an allergy specialist.

As with all allergenic extracts, severe systemic reactions may occur. In certain individuals these life-threatening reactions may result in death. Fatalities associated with skin testing have been reported. Patients should be observed for at least 20 - 30 minutes following testing. Emergency measures and adequately trained personnel should be immediately available in the event of a life-threatening reaction.

Patients with unstable asthma or steroid dependent asthmatics and patients with underlying cardiovascular disease are at greater risk to a fatal outcome from a systemic allergic reaction.

Sensitive patients may experience severe anaphlactic reactions resulting in respiratory obstruction, shock, coma and/or death. Adverse events are to be reported to MedWatch (1-800-FDA-1088), Adverse Event Reporting, Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20852-9787. This product should not be injected intravenously. Patients receiving beta blockers may not be responsive to epinephrine or inhaled bronchodilators. Respiratory obstruction not responding to parenteral or inhaled bronchodilators may require theophylline, oxygen, intubation and the use of life support systems. Parenteral fluid and/or plasma expanders may be utilized for the treatment of shock. Adrenocorticosteroids may be administered parenterally or intravenously. Refer to WARNINGS, PRECAUTIONS, and ADVERSE REACTIONS sections below.

SPL UNCLASSIFIED SECTION

Port Washington, NY 11050

U.S. Government License No. 1256

DESCRIPTION

Sterile diagnostic extracts are supplied in either phenol-saline diluent for Intradermal Testing or in diluent containing glycerin 50% (v/v) for Percutaneous Testing and phenol 0.4% (preservative). Inactive ingredients may include: sodium chloride for isotonicity, glycerin, and sodium bicarbonate as a bufferPollens are individually extracted from pure pollen extracted in a phenol-preserved sodium bicarbonate solution. Short Ragweed and Mixed (Tall and Short) Ragweed extracts are standardized by Antigen E content and so labeled. The Antigen E content of extracts containing Short Ragweed at a concentration more dilute than a weight/volume ratio of 1:10 are obtained by calculating the Antigen E content based on the assay value of more concentrated extract. Pollen extracts are filtered aseptically and after final packaging, they are tested for sterility and safety. Molds are individually extracted from pure powdered inactivated mold source material extracted in phenol preserved saline.Mold extracts are filtered aseptically and after final packaging are tested for sterility and safety.

Molds (fungi) are present in all inhabited places at all seasons of the year; they are so ubiquitous that they are prevalent at times when common allergic pollens and other inhalants are not. In the home and surroundings, molds are found in upholstered furniture, mattresses, drapes, cellar and storage room dust, woolens, leather goods, fruits, meats, cheeses, garden soil and on plants. Spores, mycelial fragments and mold residues are thus inhaled, contacted and ingested continuously.

Foods, miscellaneous inhalants and epidermals are individually extracted in phenol preserved saline or glycerin, filtered aseptically and after final packaging are tested for sterility and safety.

CLINICAL PHARMACOLOGY

Diagnostically (for skin testing) the allergen combines with IgE antibodies fixed to mast cells in the skin. This complexing causes an increase in cellular permeability and degranulation of the mast cells releasing chemical mediators. These mediators (such as histamine) are responsible for a local inflammatory response of wheal and erythema typical of a positive skin test reaction and also, the symptoms commonly associated with allergic disease.1 The more mediator release, the larger the reaction (wheal and erythema).

INDICATIONS AND USAGE

These products are for diagnostic use only. Diagnostic allergenic extracts are indicated for use in skin testing to establish the clinical relevance of specific allergens to which the patient has been exposed. By measuring skin test response the physician may assess the degree of sensitivity that patients have to the allergens. For extracts standardized in AU and BAU, see individual directions for use. Allergenic extracts for diagnostic use only of coffee, mosquito, cottonseed, and flaxseed have not been shown by adequate data to be safe and effective for therapeutic use.

CONTRAINDICATIONS

Patients on beta blockers can be non-responsive to beta agonists that may be required to reverse a systemic reaction (also, see boxed WARNING statement and ADVERSE REACTIONS). The physician should carefully weigh the benefit derived from skin testing vs. the risk to the patient should a systemic reaction arise.

Patients with unstable asthma or steroid dependent asthmatics and patients with underlying cardiovascular disease are at greater risk to a fatal outcome from a systemic allergic reaction2,3. See also PRECAUTIONS and ADVERSE REACTIONS.

WARNING

Patients should always be observed for at least 20 - 30 minutes after skin testing. In the event of a marked systemic reaction such as urticaria, angioedema, wheezing, dyspnea, respiratory obstruction, hypotension, coma and death (see ADVERSE REACTIONS), applications of a tourniquet above the injection site and administration of 0.2 mL to 1 mL (0.01 mg/kg) of epinephrine injection (1:1,000) are recommended. Maximal recommended dose for children between 2 and 12 years of age is 0.5 mL. The tourniquet is then gradually released at 15 minute intervals. Patients under treatment with beta blockers may be refractory to the usual dose of epinephrine.

Volume expanders and vasopressor agents may be required to reverse hypotension, inhalation bronchodilators and parenteral aminophylline may be required to reverse bronchospasm. In case of respiratory obstruction, oxygen and intubation may be necessary. Life-threatening reactions unresponsive to the above may require cardiopulmonary resuscitation.

PRECAUTIONS

INFORMATION FOR PATIENTS:

Patients should be instructed to describe any active allergic symptoms such as rhinitis, wheezing, dyspnea, etc. prior to testing. Also, see ADVERSE REACTIONS and WARNINGS Sections.

Patients should always be observed 20 to 30 minutes after testing.

General:

1. In the presence of active symptoms such as rhinitis, wheezing, dyspnea, etc., the indications for skin testing must be weighed carefully against the risk of temporarily aggravating the symptoms by the testing itself. Objective assessment of pulmonary function such as Peak Expiratory Flow Rate (PEFR) before allergen administration and prior to discharge may be useful in unstable asthmatics to reduce the chances of exacerbation of the patient’s asthma. Patients should be instructed to describe any active allergic symptoms as described above prior to skin testing and encouraged to report any late reactions from this testing. Also, see ADVERSE REACTIONS and WARNING sections.
   
2. Store allergenic extracts between 2°-8°C at all times, even during use.
   
3. Care must be taken to avoid drawing blood.
   1. For percutaneous testing, if blood is observed, immediately wipe the allergen from the site.
      
   2. For intradermal skin testing, pull gently on the syringe plunger and note if any blood enters the syringe. If blood is obtained, reposition the needle and repeat before injecting (see DOSAGE AND ADMINISTRATION).
   
   
4. Allergenic extracts become less potent with age. Allergenic extracts containing glycerin 50% v/v are relatively stable. Non-glycerinated aqueous extracts, particularly dilute forms as used for intradermal skin testing, have been shown to be extremely unstable. Until such time as stability studies are complete with dilute allergens, new intradermal strength materials should be prepared every few weeks.
   
5. Use standard aseptic precautions if making dilutions from stock concentrates to intradermal strength.
   
6. For intradermal testing: Extracts in glycerin 50% v/v must be diluted with a non-glycerinated diluent and must be diluted at least 25-fold to less than 2% glycerin by volume, as glycerin above this level can cause false positive intradermal skin test results.

Pregnancy - Category C: 

Animal reproduction studies have not been conducted with allergenic extracts. It is also not known whether allergenic extracts can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity.

Controlled studies of hyposensitization with moderate to high doses of allergenic extracts during conception and all trimesters of pregnancy have failed to demonstrate any risk to the fetus or to the mother4. However, on the basis of histamine’s known ability to contract the uterine muscle, the release of significant amounts of histamine from allergen exposure to skin test overdose should be avoided on theoretical grounds. Therefore, allergenic extracts should be used cautiously in a pregnant woman and only if clearly needed.

Pediatric Use:

Allergenic extracts for diagnostic use have been given safely in infants and young children. Infants have lower skin test reactivity to histamine, as well as common allergens. Skin test reactivity gradually increases to age 6 and plateaus to age 60. Therefore, small skin test reactions should be anticipated in children under age 6.

Geriatric Use: 

Skin test reactivity gradually decreases after age 60. Therefore, smaller skin test reactions should be anticipated in adults over age 60.

Nursing Mothers: 

It is not known if allergens administered subcutaneously appear in human milk. Because many drugs are excreted in human milk, caution should be exercised when allergenic extracts are administered to a nursing woman.

Carcinogenesis, mutagenesis, impairment of fertility: 

Studies in animals have not been performed.

Drug Interactions:

Drugs can interfere with the performance of skin tests5.

Antihistamines: Response to mediator (histamine) released by allergens is suppressed by antihistamines. The length of suppression varies and is dependent on individual patient, type of antihistamine and length of time the patient has been on antihistamines. The duration of this suppression may be as little as 24 hours (chlorpheniramine), and can be as long as 40 days (astemizole).

Tricyclic Antidepressants: These exert a potent and sustained decrease of skin reactivity to histamine which may last for a few weeks.

Beta2 Agonists: Oral terbutaline and parenteral ephedrine, in general, have been shown to decrease allergen induced wheal.

Dopamine: Intravenous infusion of dopamine may inhibit skin test responses.

Beta Blocking Agents: Propranolol can significantly increase skin test reactivity.

Other Drugs: Short acting steroids, inhaled beta2 agonists, theophylline and cromolyn do not seem to affect skin test response.

ADVERSE REACTIONS

Fatalities from skin testing in the United States have been extensively reviewed by Lockey.2 Six fatalities were associated with intradermal testing without previous percutaneous testing and one was associated with a combination of percutaneous (scratch) and intradermal skin testing. With careful attention to dosage and administration, fatal reactions occur infrequently, but it must be remembered that allergenic extracts are highly potent to sensitive individuals and overdosage could result in anaphylactic symptoms. Therefore it is imperative that physicians administering allergenic extracts for skin testing understand, and be prepared for the treatment of severe reactions.

Local:

Immediate wheal and erythema reactions are to be expected; but if very large, may be the first manifestation of a systemic reaction. In such cases, immediately wipe the test site(s) with sterile gauze or cotton to remove excess allergen.

Systemic Reactions: 

Systemic reactions are characterized by one or more of the following symptoms: sneezing, mild to severe generalized urticaria, itching (other than at the skin test site), extensive or generalized edema, wheezing, asthma, dyspnea, cyanosis, hypotension, syncope, and upper airway obstruction. Symptoms may progress to shock and death. Patients should always be observed for at least 20 - 30 minutes after testing.

Volume expanders and vasopressor agents may be required to reverse hypotension. Inhalational bronchodilators and parenteral aminophylline may be required to reverse bronchospasm. Severe airway obstruction unresponsive to bronchodilator may require tracheal intubation and use of oxygen. In the event of a marked systemic reaction, application of a tourniquet above the injection site and the administration of 0.2 mL to 1.0 mL of epinephrine injection (1:1,000) is recommended. Maximum recommended dose for children between 2 and 12 years of age is 0.3 mL. The tourniquet should not be left in place without loosening for 90 seconds every 15 minutes.

Adverse events should be reported via MedWatch (1-800-FDA-1088), Adverse Event Reporting, Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20852-9787.

OVERDOSAGE

Signs and symptoms of overdose are typically large local and systemic reactions. For management of overdose reactions, refer to the ADVERSE REACTIONS section above.

DOSAGE AND ADMINISTRATION

Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.

Skin test techniques for immediate (Type I) hypersensitivity testing fall into two major categories: percutaneous, and intracutaneous.

Percutaneous techniques:

For percutaneous testing, in general, skin is scratched, punctured or pricked just before the allergen is applied or through a drop of test allergen. There are several devices available for this technique. Refer to the manufacturer or distributor’s circular for specific directions for their use.

In General:

1. It is recommended that the test areas should be placed no closer than 4 - 5 cm apart to avoid interference of reactions when several tests are applied.
   
2. Skin test areas should be cleansed with alcohol and air dried.
   
3. Preferably, the allergen should be placed on the volar surface of the forearm, upper arm, or the patient’s back. The patient should be placed in a comfortable position prior to testing.
   
4. For scratch testing, a sharp, clean, sterile instrument is used to abrade the skin, but not to draw blood. Each scratch should be about 2 - 4 mm in length. A small drop of extract is placed on the surface of the skin.
   
5. Prick testing: For prick testing, a sharp, sterile instrument is used to puncture the skin slightly, applying it at a 15 - 20° angle to the skin. The instrument is gently raised, “tenting” the skin until it pops out, generally pricking through the drop of allergen. Do not draw blood.
   
6. For puncture testing, a sharp, clean, sterile instrument must be used. Puncture the skin, through the drop of allergen, perpendicular to the skin. Do not draw blood.

For all of the above techniques, a separate instrument must be used for each patient; if the instrument is to be used to pass through the allergen, to avoid cross-contamination, a separate instrument is to be used for each allergen. The test should be read in 15 minutes, measuring both wheal size and erythema.

Intracutaneous (intradermal) testing:

General: Intradermal testing is more sensitive than percutaneous testing and its specificity is dependent on dose. Intradermal testing is not intended as an initial screen unless used in highly dilute solutions. Intradermal testing is usually reserved for allergens that have demonstrated either negative or equivocal percutaneous skin test response in the face of positive or unclear history.

Intradermal testing of one allergen in several serial dilutions (beginning with the weakest to the more concentrated dilutions) may also be useful in assessing degree of patient sensitivity for the establishment of a safe starting dose for immunotherapy.

Bulk extracts must be diluted for intradermal testing. Use of Sterile Diluent for Allergenic Extracts or Sterile Diluent for Allergenic Extracts Normal Saline with HSA (albumin saline) is recommended. Dilutions should be made with sterile disposable syringes using aseptic technique. Commonly 10 fold dilutions are used to achieve a desired concentration for intradermal testing and continuation of immunotherapy. For example, transferring 0.5 mL of a 10,000 PNU/mL extract into 4.5 mL of diluent will yield 5 mL of extract at 1,000 PNU/mL. For weight volume products, a 1:100 w/v dilution may be prepared from a 1:10 w/v by transferring 0.5 mL of the 1:10 w/v to 4.5 mL of dilutent. Prepare as many additional serial dilutions as necessary to reach the appropriate concentration. As a general rule intradermal strength should begin at no higher than 1/100 to 1/1000 of the percutaneous strength that resulted in a negative skin test reaction.

1. It is recommended that the test areas should be spaced no less than 5 cm apart to avoid interference with adjacent allergen or control.
   
2. Skin should be cleansed with alcohol and air dried.
   
3. A sterile 1 mL or 1/2 mL syringe with a 26 - 30 gauge needle should be used. A separate sterile syringe should be used for each extract and each patient.
   
4. Care should be taken to eliminate air bubbles from the syringe prior to injecting the test dose. It is suggested that not more than 6 - 10 allergens of each different type be used at any one time. Very sensitive patients may show rapid response.
   
5. The skin is held tensely, and the needle is inserted almost parallel to the skin, beveled side up far enough to cover the beveled portion. Slowly inject sufficient extract to make a small bleb of approximately 5 mm in diameter (0.01 - 0.02 mL).
   
6. Read the test results in 15 minutes.

Selection of the proper strength for intracutaneous testing: A general rule for the prevention of untoward reactions, particularly in extremely sensitive patients, is to screen by percutaneous methods initially, and begin intradermal testing at a strength not more than 1/100 of a negative or equivocal percutaneous reaction.

Controls:

In both percutaneous and intracutaneous tests, a negative control test with diluent alone should be performed because some patients exhibit dermographia, and/or other non-specific irritant responses.

As a positive control in the evaluation of allergenic skin testing, histamine 1 mg/mL (histamine base) should be used for percutaneous testing, and histamine 0.1 mg/mL (histamine base) should be used for intradermal testing.

Interpretation of results:

Patient’s response is graded on the basis of the size of erythema or wheal.6 General guidelines follow for percutaneous testing, different devices and/or techniques influence the size of the reaction, therefore it is important to refer to the device manufacturer’s or distributor’s instructions when grading reactions.

Percutaneous (prick or scratch) test:

0       No reaction or less than control.

+       Erythema greater than control, smaller than a nickel (21 mm diameter).

++       Erythema greater than a nickel in diameter, no wheal.

+++ Wheal and erythema without pseudopods.

++++ Wheal and erythema with pseudopods.

Intradermal test:

0       No reaction or less than negative control.

+       3-4 mm wheal with erythema, or erythema alone larger than a nickel (21 mm diameter).

++       4-8 mm wheal and erythema, without pseudopods.

+++ Over 8 mm wheal and erythema without pseudopods.

++++ Wheal and erythema with pseudopods.

HOW SUPPLIED

For scratch and prick testing: 5 mL dropper applicator vials in 50% v/v glycerin or 10mL stoppered vial in 50% v/v glycerin. Available individually and in a complete set of the most common allergens. Available in either Protein Nitrogen Units (PNU/mL) or weight to volume (w/v).

For intracutaneous testing: 5 mL sterile vials, aqueous based, individually and in a complete set of the most common allergens. Available in either Protein Nitrogen Units (PNU/mL) or weight to volume (w/v).

Histatrol® Positive skin test control - histamine. 1 mg/mL and 0.1 mg/mL histamine base.

See Product Catalog for specific diagnostic concentrations available.

STORAGE

To maintain stability of allergenic extracts, proper storage conditions are essential. Bulk concentrates and diluted extracts are to be stored at 2º to 8ºC even during use. Bulk or diluted extracts are not to be frozen. Do not use after the expiration date shown on the vial label.

REFERENCES

1. Holgate, S.T., Robinson, C. and Church, M.K. Mediators of immediate hypersensitivity. In Middleton et al: Allergy Principles and Practice, St. Louis, 1988, C.V. Mosby, p 135.
   
2. Lockey, R.F., et al. Fatalities from immunotherapy (IT) and skin testing (ST). J. Allergy Clin. Immunol. 1987: 79: 660.
   
3. Reid, M.J. et al. Survey of fatalities from skin testing and immunotherapy. 1985-1989. J. Allergy Clin Immunol. 1993; 92:6.
   
4. DeBuske L. M. et al. Special problems regarding Allergen Immunotherapy in Immunology and Allergy Clinics of North America, Greenburger, P.A. Ed. February 1992; 145-149.
   
5. Bousquet, J. In vivo methods for the study of allergy: skin test, techniques and interpretation. In: Middleton et al.: Allergy Principles and Practice 3rd Ed. St. Louis: CV Mosby, 1988:167.
   
6. Freedman, S.O. Asthma and Allergic Rhinitis II. Clinical Aspects, in Freedman and Gold Clinical Immunology 2nd Ed. New York: Harper & Row, 1976: 131.

Revised  April 2017                   No. 112R      

© ALK-Abelló, Inc.

Distributed in Canada by:
ALK-Abelló Pharmaceuticals, Inc.
#35-151 Brunel Road
Mississauga, Ontario
Canada L4Z 2H6

PRINCIPAL DISPLAY PANEL

ALLERGENIC EXTRACT
DIN 00299987
5mL sterile multiple dose vial
FOR PERCUTANEOUS TESTING ONLY

INGREDIENTS AND APPEARANCE

HOUSE DUST 
house dust injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6000
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOUSE DUST (UNII: EYO007VX98) (HOUSE DUST - UNII:EYO007VX98)	HOUSE DUST	10000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6000-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965	06/30/2013

ALMOND 
almond food injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6100
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALMOND (UNII: 3Z252A2K9G) (ALMOND - UNII:3Z252A2K9G)	ALMOND	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6100-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

APPLE 
apple food injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6101
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
APPLE (UNII: B423VGH5S9) (APPLE - UNII:B423VGH5S9)	APPLE	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6101-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

APRICOT 
apricot injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6102
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
APRICOT (UNII: 269CJD5GZ9) (APRICOT - UNII:269CJD5GZ9)	APRICOT	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6102-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ASPARAGUS 
asparagus injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6103
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPARAGUS (UNII: Z1EJP3037Z) (ASPARAGUS - UNII:Z1EJP3037Z)	ASPARAGUS	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6103-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AVOCADO 
avocado injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6104
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOCADO (UNII: SDS87L369F) (AVOCADO - UNII:SDS87L369F)	AVOCADO	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6104-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BANANA 
banana injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6105
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BANANA (UNII: 4AJZ4765R9) (BANANA - UNII:4AJZ4765R9)	BANANA	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6105-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BARLEY 
barley food injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6106
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BARLEY (UNII: 5PWM7YLI7R) (BARLEY - UNII:5PWM7YLI7R)	BARLEY	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6106-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BEAN 
pinto bean kidney bean injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6107
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BEAN (UNII: 8WB9PV3YW5) (BEAN - UNII:8WB9PV3YW5)	BEAN	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6107-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

STRING BEAN 
string bean green bean injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6108
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
STRING BEAN (UNII: N9D69B2Q7Y) (STRING BEAN - UNII:N9D69B2Q7Y)	STRING BEAN	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6108-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BEEF 
beef injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6109
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BEEF (UNII: 4PIB2155QP) (BEEF - UNII:4PIB2155QP)	BEEF	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6109-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BRAZIL NUT 
brazil nut injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6110
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BRAZIL NUT (UNII: XKR79OET1K) (BRAZIL NUT - UNII:XKR79OET1K)	BRAZIL NUT	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6110-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BROCCOLI 
broccoli injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6112
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BROCCOLI (UNII: UOI4FT57BZ) (BROCCOLI - UNII:UOI4FT57BZ)	BROCCOLI	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6112-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BUCKWHEAT 
buckwheat injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6113
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BUCKWHEAT (UNII: N0Y68724R3) (BUCKWHEAT - UNII:N0Y68724R3)	BUCKWHEAT	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6113-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CABBAGE 
cabbage injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6114
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CABBAGE (UNII: GW0W1Y9I97) (CABBAGE - UNII:GW0W1Y9I97)	CABBAGE	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6114-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CANTALOUPE 
cantaloupe injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6115
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CANTALOUPE (UNII: 8QF5D5H6UH) (CANTALOUPE - UNII:8QF5D5H6UH)	CANTALOUPE	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6115-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CARROT 
carrot injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6116
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CARROT (UNII: L56Z1JK48B) (CARROT - UNII:L56Z1JK48B)	CARROT	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6116-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CASEIN 
casein injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6118
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CASEIN (UNII: 48268V50D5) (CASEIN - UNII:48268V50D5)	CASEIN	0.01 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6118-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CELERY 
celery injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6120
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CELERY (UNII: 44IDY6DTKX) (CELERY - UNII:44IDY6DTKX)	CELERY	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6120-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CHERRY 
cherry injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6121
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHERRY (UNII: BUC5I9595W) (CHERRY - UNII:BUC5I9595W)	CHERRY	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6121-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CHICKEN 
chicken meat injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6122
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHICKEN (UNII: 0X8Q245Y7B) (CHICKEN - UNII:0X8Q245Y7B)	CHICKEN	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6122-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CINNAMON 
cinnamon injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6123
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CINNAMON (UNII: 5S29HWU6QB) (CINNAMON - UNII:5S29HWU6QB)	CINNAMON	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6123-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CLAM 
clam injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6124
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
QUAHOG, UNSPECIFIED (UNII: 226LY0AFR9) (QUAHOG, UNSPECIFIED - UNII:226LY0AFR9)	QUAHOG, UNSPECIFIED	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6124-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

COCOA BEAN 
cocoa bean whole bean chocolate injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6125
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COCOA (UNII: D9108TZ9KG) (COCOA - UNII:D9108TZ9KG)	COCOA	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6125-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

COCONUT 
coconut injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6127
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COCONUT (UNII: 3RT3536DHY) (COCONUT - UNII:3RT3536DHY)	COCONUT	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6127-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CODFISH 
codfish injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6128
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COD, UNSPECIFIED (UNII: 8D6Q5LNG3D) (COD, UNSPECIFIED - UNII:8D6Q5LNG3D)	COD, UNSPECIFIED	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6128-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

COFFEE BEAN 
coffee injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6129
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COFFEE BEAN (UNII: JFH385Y744) (COFFEE BEAN - UNII:JFH385Y744)	COFFEE BEAN	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6129-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CRAB 
crab leg, unspecified injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6130
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CRAB LEG, UNSPECIFIED (UNII: S1VF61QLO9) (CRAB LEG, UNSPECIFIED - UNII:S1VF61QLO9)	CRAB LEG, UNSPECIFIED	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6130-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CUCUMBER 
cucumber injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6132
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CUCUMBER (UNII: YY7C30VXJT) (CUCUMBER - UNII:YY7C30VXJT)	CUCUMBER	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6132-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

EGG WHITE 
egg white injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6133
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EGG WHITE (UNII: 3E0I92Z2GR) (EGG WHITE - UNII:3E0I92Z2GR)	EGG WHITE	0.01 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6133-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

EGG 
whole egg injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6135
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EGG (UNII: 291P45F896) (EGG - UNII:291P45F896)	EGG	0.01 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6135-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

EGG YOLK 
egg yolk injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6136
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EGG YOLK (UNII: 4IPS17B70T) (EGG YOLK - UNII:4IPS17B70T)	EGG YOLK	0.01 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6136-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

FLOUNDER 
flounder injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6137
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
FLOUNDER, UNSPECIFIED (UNII: T197LO581X) (FLOUNDER, UNSPECIFIED - UNII:T197LO581X)	FLOUNDER, UNSPECIFIED	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6137-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

GARLIC 
garlic injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6138
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GARLIC (UNII: V1V998DC17) (GARLIC - UNII:V1V998DC17)	GARLIC	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6138-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

GRAPE 
white seedless grape injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6139
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GRAPE (UNII: 6X543N684K) (GRAPE - UNII:6X543N684K)	GRAPE	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6139-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

GRAPEFRUIT 
grapefruit injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6141
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GRAPEFRUIT (UNII: O82C39RR8C) (GRAPEFRUIT - UNII:O82C39RR8C)	GRAPEFRUIT	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6141-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

KARAYA GUM 
karaya gum bassora injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6143
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
KARAYA GUM (UNII: 73W9IQY50Q) (KARAYA GUM - UNII:73W9IQY50Q)	KARAYA GUM	0.005 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6143-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

HONEYDEW MELON 
honeydew injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6146
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HONEYDEW MELON (UNII: RN8P45F92A) (HONEYDEW MELON - UNII:RN8P45F92A)	HONEYDEW MELON	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6146-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

LAMB 
lamb injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6149
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LAMB (UNII: FOF26T73HA) (LAMB - UNII:FOF26T73HA)	LAMB	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6149-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

LEMON 
lemon injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6170
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LEMON (UNII: 24RS0A988O) (LEMON - UNII:24RS0A988O)	LEMON	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6170-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

LETTUCE 
lettuce injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6171
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LETTUCE (UNII: 5PO6NN3RRJ) (LETTUCE - UNII:5PO6NN3RRJ)	LETTUCE	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6171-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

LIMA BEAN 
lima bean injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6173
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIMA BEAN (UNII: 112YH1ZMX2) (LIMA BEAN - UNII:112YH1ZMX2)	LIMA BEAN	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6173-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

LOBSTER 
lobster injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6174
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LOBSTER, UNSPECIFIED (UNII: ZQ6LG2C39M) (LOBSTER, UNSPECIFIED - UNII:ZQ6LG2C39M)	LOBSTER, UNSPECIFIED	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6174-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

GOAT MILK 
goat milk injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6177
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GOAT MILK (UNII: XE5K5I4RP7) (GOAT MILK - UNII:XE5K5I4RP7)	GOAT MILK	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6177-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

COW MILK 
milk whole cows injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6178
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COW MILK (UNII: 917J3173FT) (COW MILK - UNII:917J3173FT)	COW MILK	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6178-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

MUSHROOM 
mushroom agaricus spp injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6180
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CULTIVATED MUSHROOM (UNII: 54C8E6W6JY) (CULTIVATED MUSHROOM - UNII:54C8E6W6JY)	CULTIVATED MUSHROOM	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6180-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

MUSTARD SEED 
mustard seed injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6181
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MUSTARD SEED (UNII: 58RXI817UT) (MUSTARD SEED - UNII:58RXI817UT)	MUSTARD SEED	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6181-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

OAT 
oat grain injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6183
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OAT (UNII: Z6J799EAJK) (OAT - UNII:Z6J799EAJK)	OAT	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6183-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BLACK OLIVE 
olive injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6185
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BLACK OLIVE (UNII: 2M6QWV94OC) (BLACK OLIVE - UNII:2M6QWV94OC)	BLACK OLIVE	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6185-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ONION 
onion injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6186
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ONION (UNII: 492225Q21H) (ONION - UNII:492225Q21H)	ONION	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6186-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ORANGE 
orange injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6187
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ORANGE (UNII: 5EVU04N5QU) (ORANGE - UNII:5EVU04N5QU)	ORANGE	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6187-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

OYSTER 
oyster injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6189
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OYSTER, UNSPECIFIED (UNII: S614XWR17V) (OYSTER, UNSPECIFIED - UNII:S614XWR17V)	OYSTER, UNSPECIFIED	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6189-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PEA 
green pea english injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6191
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PEA (UNII: W4X7H8GYFM) (PEA - UNII:W4X7H8GYFM)	PEA	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6191-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PEACH 
peach injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6192
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PEACH (UNII: 3OKE88I3QG) (PEACH - UNII:3OKE88I3QG)	PEACH	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6192-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PEANUT 
peanut injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6193
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PEANUT (UNII: QE1QX6B99R) (PEANUT - UNII:QE1QX6B99R)	PEANUT	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6193-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PEAR 
pear injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6195
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PEAR (UNII: 2ZN8DWC0YF) (PEAR - UNII:2ZN8DWC0YF)	PEAR	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6195-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PECAN 
pecan injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6196
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PECAN (UNII: F14P91GB5F) (PECAN - UNII:F14P91GB5F)	PECAN	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6196-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

GREEN BELL PEPPER 
bell injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6197
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GREEN BELL PEPPER (UNII: 4J4DOU3HEK) (GREEN BELL PEPPER - UNII:4J4DOU3HEK)	GREEN BELL PEPPER	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6197-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BLACK PEPPER 
black pepper injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6198
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BLACK PEPPER (UNII: KM66971LVF) (BLACK PEPPER - UNII:KM66971LVF)	BLACK PEPPER	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6198-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PINEAPPLE 
pineapple injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6200
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PINEAPPLE (UNII: 2A88ZO081O) (PINEAPPLE - UNII:2A88ZO081O)	PINEAPPLE	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6200-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PISTACHIO 
pistachio nut injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6202
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PISTACHIO (UNII: 6815CPT6ZJ) (PISTACHIO - UNII:6815CPT6ZJ)	PISTACHIO	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6202-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PLUM 
plum injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6203
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PLUM (UNII: 67M3EQ6BE1) (PLUM - UNII:67M3EQ6BE1)	PLUM	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6203-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PORK 
pork injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6204
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PORK (UNII: O138UB266J) (PORK - UNII:O138UB266J)	PORK	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6204-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

POTATO 
sweet potato injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6205
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POTATO (UNII: CFE1S8DYWD) (POTATO - UNII:CFE1S8DYWD)	POTATO	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6205-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

POTATO 
white potato injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6206
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POTATO (UNII: CFE1S8DYWD) (POTATO - UNII:CFE1S8DYWD)	POTATO	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6206-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

RICE 
brown rice injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6208
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BROWN RICE (UNII: 659G217HPG) (BROWN RICE - UNII:659G217HPG)	BROWN RICE	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6208-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

RYE 
rye injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6210
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RYE (UNII: 0R4AQI398X) (RYE - UNII:0R4AQI398X)	RYE	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6210-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SALMON 
salmon injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6212
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALMON, UNSPECIFIED (UNII: 6122W2M0GB) (SALMON, UNSPECIFIED - UNII:6122W2M0GB)	SALMON, UNSPECIFIED	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6212-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SESAME SEED 
sesame seed injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6213
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SESAME SEED (UNII: 7Y1255HVXR) (SESAME SEED - UNII:7Y1255HVXR)	SESAME SEED	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6213-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SHRIMP 
shrimp injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6214
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SHRIMP, UNSPECIFIED (UNII: 1891LE191T) (SHRIMP, UNSPECIFIED - UNII:1891LE191T)	SHRIMP, UNSPECIFIED	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6214-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SOYBEAN 
soybean injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6216
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SOYBEAN (UNII: L7HT8F1ZOD) (SOYBEAN - UNII:L7HT8F1ZOD)	SOYBEAN	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6216-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SPINACH 
spinach injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6218
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SPINACH (UNII: 6WO75C6WVB) (SPINACH - UNII:6WO75C6WVB)	SPINACH	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6218-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SQUASH 
squash injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6219
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SQUASH (UNII: 9961HBA483) (SQUASH - UNII:9961HBA483)	SQUASH	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6219-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

STRAWBERRY 
strawberry injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6220
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
STRAWBERRY (UNII: 4J2TY8Y81V) (STRAWBERRY - UNII:4J2TY8Y81V)	STRAWBERRY	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6220-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CORN 
sweet corn injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6221
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CORN (UNII: 0N8672707O) (CORN - UNII:0N8672707O)	CORN	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6221-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

TOMATO 
tomato injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6224
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOMATO (UNII: Z4KHF2C175) (TOMATO - UNII:Z4KHF2C175)	TOMATO	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6224-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

TUNA 
tuna injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6226
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TUNA, UNSPECIFIED (UNII: V2T3IHT3E2) (TUNA, UNSPECIFIED - UNII:V2T3IHT3E2)	TUNA, UNSPECIFIED	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6226-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

TURKEY 
turkey meat injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6229
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TURKEY (UNII: 8E9NT44R8I) (TURKEY - UNII:8E9NT44R8I)	TURKEY	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6229-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

VANILLA 
vanilla injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6230
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
VANILLA (UNII: Q74T35078H) (VANILLA - UNII:Q74T35078H)	VANILLA	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6230-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ENGLISH WALNUT 
english walnut injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6231
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ENGLISH WALNUT (UNII: 1V3SHR7QB7) (ENGLISH WALNUT - UNII:1V3SHR7QB7)	ENGLISH WALNUT	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6231-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

WATERMELON 
watermelon injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6233
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WATERMELON (UNII: 231473QB6R) (WATERMELON - UNII:231473QB6R)	WATERMELON	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6233-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

WHEAT 
whole wheat wheat grain injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6234
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WHEAT (UNII: 4J2I0SN84Y) (WHEAT - UNII:4J2I0SN84Y)	WHEAT	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6234-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BOS TAURUS SKIN 
cattle epithelium injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6300
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BOS TAURUS SKIN (UNII: 7J12CD6O9L) (BOS TAURUS SKIN - UNII:7J12CD6O9L)	BOS TAURUS SKIN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6300-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

COTTON FIBER 
cattle epithelium injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6302
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COTTON FIBER (UNII: 70LDW53ROO) (COTTON FIBER - UNII:70LDW53ROO)	COTTON FIBER	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6302-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

COTTON SEED 
cottonseed injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6304
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COTTON SEED (UNII: DI0ZRJ0MXN) (COTTON SEED - UNII:DI0ZRJ0MXN)	COTTON SEED	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6304-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CANIS LUPUS FAMILIARIS SKIN 
dog epithelium injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6306
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CANIS LUPUS FAMILIARIS SKIN (UNII: X2W7CLE97T) (CANIS LUPUS FAMILIARIS SKIN - UNII:X2W7CLE97T)	CANIS LUPUS FAMILIARIS SKIN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6306-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CAVIA PORCELLUS SKIN 
guinea pig epithelium injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6309
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAVIA PORCELLUS SKIN (UNII: GM3H4U6QS8) (CAVIA PORCELLUS SKIN - UNII:GM3H4U6QS8)	CAVIA PORCELLUS SKIN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6309-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

EQUUS CABALLUS SKIN 
horse epithelium injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6311
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EQUUS CABALLUS SKIN (UNII: 88VZV9HGT4) (EQUUS CABALLUS SKIN - UNII:88VZV9HGT4)	EQUUS CABALLUS SKIN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6311-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CEIBA PENTANDRA FIBER 
kapok injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6312
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CEIBA PENTANDRA FIBER (UNII: 758Z9H9WV9) (CEIBA PENTANDRA FIBER - UNII:758Z9H9WV9)	CEIBA PENTANDRA FIBER	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6312-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

MUS MUSCULUS SKIN 
mouse epithelium injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6314
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MUS MUSCULUS SKIN (UNII: 390AN9GB09) (MUS MUSCULUS SKIN - UNII:390AN9GB09)	MUS MUSCULUS SKIN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6314-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ORRIS 
iris x germanica root injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6317
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
IRIS X GERMANICA ROOT (UNII: 8N6VTJ9IWV) (IRIS X GERMANICA ROOT - UNII:8N6VTJ9IWV)	IRIS X GERMANICA ROOT	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6317-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PYRETHRUM CINERARIIFOLIUM 
pyrethrum injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6318
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TANACETUM CINERARIIFOLIUM FLOWER (UNII: CGF76TP7X6) (TANACETUM CINERARIIFOLIUM FLOWER - UNII:CGF76TP7X6)	TANACETUM CINERARIIFOLIUM FLOWER	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6318-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

RABBIT 
rabbit epithelium injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6320
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RABBIT (UNII: O5V0F26RUW) (RABBIT - UNII:O5V0F26RUW)	RABBIT	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6320-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SOLENOPSIS INVICTA 
fire ant injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6400
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SOLENOPSIS INVICTA (UNII: 5O7CR4P444) (SOLENOPSIS INVICTA - UNII:5O7CR4P444)	SOLENOPSIS INVICTA	0.01 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6400-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PERIPLANETA AMERICANA 
american cockroach injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6403
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (PERIPLANETA AMERICANA - UNII:2RQ1L9N089)	PERIPLANETA AMERICANA	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6403-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BLATELLA GERMANICA 
german cockroach injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6405
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BLATTELLA GERMANICA (UNII: G9O67I0A8Q) (BLATTELLA GERMANICA - UNII:G9O67I0A8Q)	BLATTELLA GERMANICA	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6405-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ACREMONIUM STRICTUM 
acremonium strictum injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6500
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SAROCLADIUM STRICTUM (UNII: 3F36V0451W) (SAROCLADIUM STRICTUM - UNII:3F36V0451W)	SAROCLADIUM STRICTUM	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6500-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ALTERNARIA TENUIS 
alternaria tenuis a alternata injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6502
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6502-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ASPERGILLUS FUMIGATUS 
aspergillus fumigatus injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6504
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48)	ASPERGILLUS FUMIGATUS	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6504-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ASPERGILLUS NIGER VAR NIGER 
aspergillus niger injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6507
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6507-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AUREOBASIDIUM PULLULANS VAR PULLULANS 
pullularia pullulans injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6509
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK)	AUREOBASIDIUM PULLULANS VAR. PULLUTANS	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6509-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BOTRYTIS CINEREA 
botrytis cinerea injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6512
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7)	BOTRYTIS CINEREA	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6512-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CANDIDA ALBICANS 
candida albicans injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6514
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC)	CANDIDA ALBICANS	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6514-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CHAETOMIUM GLOBOSUM 
chaetomium globosum injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6516
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A)	CHAETOMIUM GLOBOSUM	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6516-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CLADOSPORIUM CLADOSPORIOIDES 
cladosporium cladosporioides hormodendrum clad injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6518
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLADOSPORIUM CLADOSPORIOIDES (UNII: 4ZWY20GTGO) (CLADOSPORIUM CLADOSPORIOIDES - UNII:4ZWY20GTGO)	CLADOSPORIUM CLADOSPORIOIDES	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6518-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CLADOSPORIUM SPHAEROSPERMUM 
cladosporium sphaerospermum hormodendrum hordei injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6520
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R)	CLADOSPORIUM SPHAEROSPERMUM	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6520-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

COCHLIOBOLUS SATIVUS 
helminthosporium sorokinianum injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6524
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W)	COCHLIOBOLUS SATIVUS	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6524-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

EPICOCCUM NIGRUM 
epicoccum nigrum injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6526
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7)	EPICOCCUM NIGRUM	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6526-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

FUSARIUM OXYSPORUM VASINFECTUM 
fusarium spp injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6529
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
FUSARIUM OXYSPORUM VASINFECTUM (UNII: 6M98DC08TZ) (FUSARIUM OXYSPORUM VASINFECTUM - UNII:6M98DC08TZ)	FUSARIUM OXYSPORUM VASINFECTUM	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6529-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

HELMINTHOSPORIUM SOLANI 
helminthosporium solani spondylocladium injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6533
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HELMINTHOSPORIUM SOLANI (UNII: U6Z259H815) (HELMINTHOSPORIUM SOLANI - UNII:U6Z259H815)	HELMINTHOSPORIUM SOLANI	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6533-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

MUCOR PLUMBEUS 
mucor spp injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6536
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E)	MUCOR PLUMBEUS	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6536-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

NEUROSPORA INTERMEDIA 
neurospora spp injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6538
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI)	NEUROSPORA INTERMEDIA	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6538-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

KHUSKIA ORYZAE 
nigrospora spp injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6540
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
KHUSKIA ORYZAE (UNII: VK8C112WTS) (KHUSKIA ORYZAE - UNII:VK8C112WTS)	KHUSKIA ORYZAE	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6540-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PHOMA EXIGUA VAR EXIGUA 
phoma herbarum injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6543
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PHOMA EXIGUA VAR. EXIGUA (UNII: 8JAG41IE4M) (PHOMA EXIGUA VAR. EXIGUA - UNII:8JAG41IE4M)	PHOMA EXIGUA VAR. EXIGUA	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6543-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

RHIZOPUS ARRHIZUS VAR ARRHIZUS 
rhizopus spp injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6545
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHIZOPUS ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS - UNII:8476849N1Y)	RHIZOPUS ARRHIZUS	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6545-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

RHODOTORULA RUBRA 
rhodotorula rubra injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6548
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHODOTORULA RUBRA (UNII: 15W81V867R) (RHODOTORULA RUBRA - UNII:15W81V867R)	RHODOTORULA RUBRA	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6548-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

USTILAGO MAYDIS 
corn smut injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6550
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
USTILAGO MAYDIS (UNII: 4K7Z7K7SWG) (USTILAGO MAYDIS - UNII:4K7Z7K7SWG)	USTILAGO MAYDIS	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6550-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

USTILAGO TRITICI 
wheat smut injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6552
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
USTILAGO TRITICI (UNII: BV82OL2IZ8) (USTILAGO TRITICI - UNII:BV82OL2IZ8)	USTILAGO TRITICI	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6552-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

STEMPHYLIUM SOLANI 
stemphylium spp injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6553
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
STEMPHYLIUM SOLANI (UNII: 1IEK4UDP5M) (STEMPHYLIUM SOLANI - UNII:1IEK4UDP5M)	STEMPHYLIUM SOLANI	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6553-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

TRICHOPHYTON MENTAGROPHYTES 
trichophyton mentagrophytes injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6556
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV)	TRICHOPHYTON MENTAGROPHYTES	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6556-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PENICILLIUM CHRYSOGENUM VAR CHRYSOGENUM 
yeast saccharomyces cerevisiae injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6558
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG)	PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM	0.10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6558-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ACACIA 
acacia injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6600
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACACIA (UNII: 5C5403N26O) (ACACIA - UNII:5C5403N26O)	ACACIA	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6600-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ALNUS INCANA SSP RUGOSA POLLEN 
white alder injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6601
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALNUS INCANA SUBSP. RUGOSA POLLEN (UNII: 605T96G8Y5) (ALNUS INCANA SUBSP. RUGOSA POLLEN - UNII:605T96G8Y5)	ALNUS INCANA SUBSP. RUGOSA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6601-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

MEDICAGO SATIVA POLLEN 
alfalfa injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6602
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MEDICAGO SATIVA POLLEN (UNII: G515RAI9FY) (MEDICAGO SATIVA POLLEN - UNII:G515RAI9FY)	MEDICAGO SATIVA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6602-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

FRAXINUS AMERICANA POLLEN 
white ash injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6603
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q) (FRAXINUS AMERICANA POLLEN - UNII:G684LX721Q)	FRAXINUS AMERICANA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6603-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PASPALUM NOTATUM POLLEN 
bahia grass injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6605
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK) (PASPALUM NOTATUM POLLEN - UNII:V003SHB7VK)	PASPALUM NOTATUM POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6605-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

MORELLA CERIFERA POLLEN 
bayberry wax myrtle injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6606
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MORELLA CERIFERA POLLEN (UNII: LC8MEV9S89) (MORELLA CERIFERA POLLEN - UNII:LC8MEV9S89)	MORELLA CERIFERA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6606-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

FAGUS GRANDIFOLIA POLLEN 
beech injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6607
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
FAGUS GRANDIFOLIA POLLEN (UNII: 34X886W1H4) (FAGUS GRANDIFOLIA POLLEN - UNII:34X886W1H4)	FAGUS GRANDIFOLIA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6607-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BETULA LENTA POLLEN 
black birch injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6608
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BETULA LENTA POLLEN (UNII: JQ5HI5004M) (BETULA LENTA POLLEN - UNII:JQ5HI5004M)	BETULA LENTA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6608-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BETULA NIGRA POLLEN 
river birch red injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6609
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BETULA NIGRA POLLEN (UNII: 93963RFO1P) (BETULA NIGRA POLLEN - UNII:93963RFO1P)	BETULA NIGRA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6609-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BETULA LENTA POLLEN 
white birch injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6610
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BETULA LENTA POLLEN (UNII: JQ5HI5004M) (BETULA LENTA POLLEN - UNII:JQ5HI5004M)	BETULA LENTA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6610-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ACER NEGUNDO POLLEN 
box elder ash leaf maple injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6612
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACER NEGUNDO POLLEN (UNII: P6K070AR8V) (ACER NEGUNDO POLLEN - UNII:P6K070AR8V)	ACER NEGUNDO POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6612-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AMARANTHUS PALMERI POLLEN 
carelessweed injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6613
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMARANTHUS PALMERI POLLEN (UNII: 1GH3WV23KH) (AMARANTHUS PALMERI POLLEN - UNII:1GH3WV23KH)	AMARANTHUS PALMERI POLLEN	0.025 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6613-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

JUNIPERUS ASHEI POLLEN 
mountain cedar injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6614
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
JUNIPERUS ASHEI POLLEN (UNII: 544F8MEY0Y) (JUNIPERUS ASHEI POLLEN - UNII:544F8MEY0Y)	JUNIPERUS ASHEI POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6614-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

JUNIPERUS VIRGINIANA POLLEN 
red cedar injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6615
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
JUNIPERUS VIRGINIANA POLLEN (UNII: PY0JA16R2G) (JUNIPERUS VIRGINIANA POLLEN - UNII:PY0JA16R2G)	JUNIPERUS VIRGINIANA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6615-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

XANTHIUM STRUMARIUM VAR CANADENSE POLLEN 
cocklebur injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6616
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN (UNII: 0ZK6G3W3BI) (XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN - UNII:0ZK6G3W3BI)	XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6616-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

POPULUS DELTOIDES POLLEN 
eastern cottonwood common injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6618
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POPULUS DELTOIDES POLLEN (UNII: 476DVV63WP) (POPULUS DELTOIDES POLLEN - UNII:476DVV63WP)	POPULUS DELTOIDES POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6618-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CUPRESSUS ARIZONICA POLLEN 
arizona cypress injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6619
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CUPRESSUS ARIZONICA POLLEN (UNII: 232DMH0XVF) (CUPRESSUS ARIZONICA POLLEN - UNII:232DMH0XVF)	CUPRESSUS ARIZONICA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6619-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

TAXODIUM DISTICHUM POLLEN 
bald cypress injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6620
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TAXODIUM DISTICHUM POLLEN (UNII: O12H03B41R) (TAXODIUM DISTICHUM POLLEN - UNII:O12H03B41R)	TAXODIUM DISTICHUM POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6620-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

RUMEX ACETOSELLA POLLEN 
sour dock sheep sorrel injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6621
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RUMEX ACETOSELLA POLLEN (UNII: N52MIQ81ZW) (RUMEX ACETOSELLA POLLEN - UNII:N52MIQ81ZW)	RUMEX ACETOSELLA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6621-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

RUMEX CRISPUS POLLEN 
yellow dock injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6622
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RUMEX CRISPUS POLLEN (UNII: V825XJG64G) (RUMEX CRISPUS POLLEN - UNII:V825XJG64G)	RUMEX CRISPUS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6622-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ULMUS AMERICANA POLLEN 
american elm injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6623
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ULMUS AMERICANA POLLEN (UNII: 89BAT511BD) (ULMUS AMERICANA POLLEN - UNII:89BAT511BD)	ULMUS AMERICANA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6623-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SOLIDAGO CANADENSIS POLLEN 
goldenrod injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6625
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SOLIDAGO CANADENSIS POLLEN (UNII: 644CZ16IR5) (SOLIDAGO CANADENSIS POLLEN - UNII:644CZ16IR5)	SOLIDAGO CANADENSIS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6625-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CELTIS OCCIDENTALIS POLLEN 
hackberry injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6626
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CELTIS OCCIDENTALIS POLLEN (UNII: 68R9X9Y96X) (CELTIS OCCIDENTALIS POLLEN - UNII:68R9X9Y96X)	CELTIS OCCIDENTALIS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6626-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CARYA OVATA POLLEN 
shagbark hickory injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6627
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CARYA OVATA POLLEN (UNII: 54UN9R2798) (CARYA OVATA POLLEN - UNII:54UN9R2798)	CARYA OVATA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6627-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SORGHUM HALEPENSE POLLEN 
johnson grass injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6629
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP) (SORGHUM HALEPENSE POLLEN - UNII:577VA5B4HP)	SORGHUM HALEPENSE POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6629-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

JUNIPERUS CALIFORNICA POLLEN 
western juniper injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6630
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
JUNIPERUS CALIFORNICA POLLEN (UNII: 0H1V4V5V9L) (JUNIPERUS CALIFORNICA POLLEN - UNII:0H1V4V5V9L)	JUNIPERUS CALIFORNICA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6630-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

KOCHIA SCOPARIA POLLEN 
kochia firebush injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6631
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BASSIA SCOPARIA POLLEN (UNII: 07A108ZKW5) (BASSIA SCOPARIA POLLEN - UNII:07A108ZKW5)	BASSIA SCOPARIA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6631-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CHENOPODIUM ALBUM POLLEN 
lambs quarters injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6632
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN) (CHENOPODIUM ALBUM POLLEN - UNII:098LKX5NCN)	CHENOPODIUM ALBUM POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6632-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ACER RUBRUM POLLEN 
red maple injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6634
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACER RUBRUM POLLEN (UNII: 700NK45C76) (ACER RUBRUM POLLEN - UNII:700NK45C76)	ACER RUBRUM POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6634-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ACER SACCHARUM POLLEN 
sugar maple injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6635
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACER SACCHARUM POLLEN (UNII: V38QUQ7861) (ACER SACCHARUM POLLEN - UNII:V38QUQ7861)	ACER SACCHARUM POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6635-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

IVA XANTHIFOLIA POLLEN 
burweed marshelder injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6636
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CYCLACHAENA XANTHIFOLIA POLLEN (UNII: V80TPZ0T6J) (CYCLACHAENA XANTHIFOLIA POLLEN - UNII:V80TPZ0T6J)	CYCLACHAENA XANTHIFOLIA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6636-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

IVA ANNUA VAR ANNUA POLLEN 
rough marshelder injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6637
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
IVA ANNUA POLLEN (UNII: Y2U5S5PF22) (IVA ANNUA POLLEN - UNII:Y2U5S5PF22)	IVA ANNUA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6637-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PROSOPIS JULIFLORA POLLEN 
mesquite injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6638
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PROSOPIS JULIFLORA POLLEN (UNII: 6EIJ3D04MR) (PROSOPIS JULIFLORA POLLEN - UNII:6EIJ3D04MR)	PROSOPIS JULIFLORA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6638-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ARTEMISIA VULGARIS POLLEN 
common mugwort injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6639
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARTEMISIA VULGARIS POLLEN (UNII: ANT994T71D) (ARTEMISIA VULGARIS POLLEN - UNII:ANT994T71D)	ARTEMISIA VULGARIS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6639-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

MORUS RUBRA POLLEN 
red mulberry injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6640
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MORUS RUBRA POLLEN (UNII: 9LYI4RTZ52) (MORUS RUBRA POLLEN - UNII:9LYI4RTZ52)	MORUS RUBRA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6640-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

MORUS ALBA POLLEN 
white mulberry injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6641
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MORUS ALBA POLLEN (UNII: 3I9T68187H) (MORUS ALBA POLLEN - UNII:3I9T68187H)	MORUS ALBA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6641-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

QUERCUS RUBRA POLLEN 
red oak injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6642
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
QUERCUS RUBRA POLLEN (UNII: SVW19ET93C) (QUERCUS RUBRA POLLEN - UNII:SVW19ET93C)	QUERCUS RUBRA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6642-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

QUERCUS VIRGINIANA POLLEN 
virginia live oak injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6643
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
QUERCUS VIRGINIANA POLLEN (UNII: 8KDG09A4GO) (QUERCUS VIRGINIANA POLLEN - UNII:8KDG09A4GO)	QUERCUS VIRGINIANA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6643-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

QUERCUS ALBA POLLEN 
white oak injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6644
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK) (QUERCUS ALBA POLLEN - UNII:Z4Y9ZSV4KK)	QUERCUS ALBA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6644-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

OLEA EUROPAEA POLLEN 
olive pollen injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6646
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OLEA EUROPAEA POLLEN (UNII: 43R41XZ627) (OLEA EUROPAEA POLLEN - UNII:43R41XZ627)	OLEA EUROPAEA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6646-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SYAGRUS ROMANZOFFIANA POLLEN 
queen palm coco palm injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6647
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SYAGRUS ROMANZOFFIANA POLLEN (UNII: 84ZOM591BB) (SYAGRUS ROMANZOFFIANA POLLEN - UNII:84ZOM591BB)	SYAGRUS ROMANZOFFIANA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6647-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CARYA ILLINOINENSIS POLLEN 
pecan pollen injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6648
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CARYA ILLINOINENSIS POLLEN (UNII: PYO4JR720Y) (CARYA ILLINOINENSIS POLLEN - UNII:PYO4JR720Y)	CARYA ILLINOINENSIS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6648-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AMARANTHUS RETROFLEXUS POLLEN 
rough pigweed injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6649
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW) (AMARANTHUS RETROFLEXUS POLLEN - UNII:73B14PX5FW)	AMARANTHUS RETROFLEXUS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6649-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PINUS STROBUS POLLEN 
white pine injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6651
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PINUS STROBUS POLLEN (UNII: TX1ER5UV3T) (PINUS STROBUS POLLEN - UNII:TX1ER5UV3T)	PINUS STROBUS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6651-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PLANTAGO LANCEOLATA POLLEN 
english plantain injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6652
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI) (PLANTAGO LANCEOLATA POLLEN - UNII:DO87T1U2CI)	PLANTAGO LANCEOLATA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6652-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

POPULUS ALBA POLLEN 
white poplar injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6654
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POPULUS ALBA POLLEN (UNII: VU8C8SB23P) (POPULUS ALBA POLLEN - UNII:VU8C8SB23P)	POPULUS ALBA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6654-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

LIGUSTRUM VULGARE POLLEN 
privet injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6656
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIGUSTRUM VULGARE POLLEN (UNII: Y3FRX92Z0E) (LIGUSTRUM VULGARE POLLEN - UNII:Y3FRX92Z0E)	LIGUSTRUM VULGARE POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6656-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ELYMUS REPENS POLLEN 
quack grass injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6657
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ELYMUS REPENS POLLEN (UNII: ON2T85TA2O) (ELYMUS REPENS POLLEN - UNII:ON2T85TA2O)	ELYMUS REPENS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6657-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AMBROSIA TRIFIDA POLLEN 
tall ragweed giant injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6658
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMBROSIA TRIFIDA POLLEN (UNII: KU1V1898XX) (AMBROSIA TRIFIDA POLLEN - UNII:KU1V1898XX)	AMBROSIA TRIFIDA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6658-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SALSOLA KALI POLLEN 
russian thistle injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6659
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALSOLA KALI POLLEN (UNII: 2MH135KC6G) (SALSOLA KALI POLLEN - UNII:2MH135KC6G)	SALSOLA KALI POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6659-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ARTEMISIA TRIDENTATA POLLEN 
common sagebrush injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6670
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARTEMISIA TRIDENTATA POLLEN (UNII: YI19RB8YFD) (ARTEMISIA TRIDENTATA POLLEN - UNII:YI19RB8YFD)	ARTEMISIA TRIDENTATA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6670-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

LIQUIDAMBAR STYRACIFLUA POLLEN 
sweetgum injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6671
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIQUIDAMBAR STYRACIFLUA POLLEN (UNII: 5Q246DS5BS) (LIQUIDAMBAR STYRACIFLUA POLLEN - UNII:5Q246DS5BS)	LIQUIDAMBAR STYRACIFLUA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6671-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PLATANUS OCCIDENTALIS POLLEN 
american sycamore injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6672
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PLATANUS OCCIDENTALIS POLLEN (UNII: E03U1K03LK) (PLATANUS OCCIDENTALIS POLLEN - UNII:E03U1K03LK)	PLATANUS OCCIDENTALIS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6672-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

JUGLANS NIGRA POLLEN 
black pollen walnut injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6674
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (JUGLANS NIGRA POLLEN - UNII:1BV28146ZR)	JUGLANS NIGRA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6674-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AILANTHUS ALTISSIMA POLLEN 
ailanthus tree of heaven injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6677
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AILANTHUS ALTISSIMA POLLEN (UNII: 2A64U81OQ3) (AILANTHUS ALTISSIMA POLLEN - UNII:2A64U81OQ3)	AILANTHUS ALTISSIMA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6677-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

POPULUS TREMULOIDES POLLEN 
aspen injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6681
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POPULUS TREMULOIDES POLLEN (UNII: 928OC2TJDA) (POPULUS TREMULOIDES POLLEN - UNII:928OC2TJDA)	POPULUS TREMULOIDES POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6681-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

POA ANNUA POLLEN 
annual bluegrass injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6689
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POA ANNUA POLLEN (UNII: 7U437HHU5C) (POA ANNUA POLLEN - UNII:7U437HHU5C)	POA ANNUA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6689-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BROMUS INERMIS POLLEN 
brome grass injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6691
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BROMUS INERMIS POLLEN (UNII: 766QT72BK6) (BROMUS INERMIS POLLEN - UNII:766QT72BK6)	BROMUS INERMIS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6691-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ZEA MAYS POLLEN 
corn pollen injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6697
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZEA MAYS POLLEN (UNII: 74PD8J616H) (ZEA MAYS POLLEN - UNII:74PD8J616H)	ZEA MAYS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6697-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

POPULUS FREMONTII POLLEN 
fremont cottonwood injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6700
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POPULUS FREMONTII POLLEN (UNII: 426RHB4302) (POPULUS FREMONTII POLLEN - UNII:426RHB4302)	POPULUS FREMONTII POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6700-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

POPULUS DELTOIDES SSP MONILIFERA POLLEN 
western cottonwood injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6701
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN (UNII: 5928LJ1441) (POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN - UNII:5928LJ1441)	POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6701-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

EUPATORIUM CAPILLIFOLIUM POLLEN 
dog fennel injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6706
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EUPATORIUM CAPILLIFOLIUM POLLEN (UNII: B67NF86HF0) (EUPATORIUM CAPILLIFOLIUM POLLEN - UNII:B67NF86HF0)	EUPATORIUM CAPILLIFOLIUM POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6706-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ULMUS CRASSIFOLIA POLLEN 
cedar elm injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6709
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ULMUS CRASSIFOLIA POLLEN (UNII: G82398SD3I) (ULMUS CRASSIFOLIA POLLEN - UNII:G82398SD3I)	ULMUS CRASSIFOLIA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6709-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ULMUS PUMILA POLLEN 
chinese elm injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6710
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ULMUS PUMILA POLLEN (UNII: 030R993R8E) (ULMUS PUMILA POLLEN - UNII:030R993R8E)	ULMUS PUMILA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6710-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

EUCALYPTUS GLOBULUS POLLEN 
eucalyptus injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6712
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EUCALYPTUS GLOBULUS POLLEN (UNII: 7XW7TB10X9) (EUCALYPTUS GLOBULUS POLLEN - UNII:7XW7TB10X9)	EUCALYPTUS GLOBULUS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6712-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CORYLUS AMERICANA POLLEN 
hazelnut pollen injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6714
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CORYLUS AMERICANA POLLEN (UNII: ZGS382Y3AV) (CORYLUS AMERICANA POLLEN - UNII:ZGS382Y3AV)	CORYLUS AMERICANA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6714-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ROBINIA PSEUDOACACIA POLLEN 
black locust injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6722
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ROBINIA PSEUDOACACIA POLLEN (UNII: 8003NOJ82F) (ROBINIA PSEUDOACACIA POLLEN - UNII:8003NOJ82F)	ROBINIA PSEUDOACACIA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6722-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

MELALEUCA QUINQUENERVIA POLLEN 
melaleuca pollen injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6728
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MELALEUCA QUINQUENERVIA POLLEN (UNII: NX974IRT8E) (MELALEUCA QUINQUENERVIA POLLEN - UNII:NX974IRT8E)	MELALEUCA QUINQUENERVIA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6728-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CHENOPODIUM AMBROSIOIDES POLLEN 
mexican tea injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6731
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHENOPODIUM AMBROSIOIDES POLLEN (UNII: WIB701MW2H) (CHENOPODIUM AMBROSIOIDES POLLEN - UNII:WIB701MW2H)	CHENOPODIUM AMBROSIOIDES POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6731-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965	06/30/2013

QUERCUS AGRIFOLIA POLLEN 
california live oak coast injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6736
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
QUERCUS AGRIFOLIA POLLEN (UNII: VOT5MA71M7) (QUERCUS AGRIFOLIA POLLEN - UNII:VOT5MA71M7)	QUERCUS AGRIFOLIA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6736-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

QUERCUS ALBA POLLEN 
wild pollen oat injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6741
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK) (QUERCUS ALBA POLLEN - UNII:Z4Y9ZSV4KK)	QUERCUS ALBA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6741-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SCHINUS MOLLE POLLEN 
california pepper tree injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6743
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SCHINUS MOLLE POLLEN (UNII: M0G28FH9K1) (SCHINUS MOLLE POLLEN - UNII:M0G28FH9K1)	SCHINUS MOLLE POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6743-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AMARANTHUS SPINOSUS POLLEN 
spiny pigweed injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6744
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMARANTHUS SPINOSUS POLLEN (UNII: 380W4HYR6N) (AMARANTHUS SPINOSUS POLLEN - UNII:380W4HYR6N)	AMARANTHUS SPINOSUS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6744-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CASUARINA EQUISETIFOLIA POLLEN 
australian pine beefwood injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6745
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CASUARINA EQUISETIFOLIA POLLEN (UNII: OZJ4OE173N) (CASUARINA EQUISETIFOLIA POLLEN - UNII:OZJ4OE173N)	CASUARINA EQUISETIFOLIA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6745-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PINUS ECHINATA POLLEN 
yellow pine injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6748
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PINUS ECHINATA POLLEN (UNII: 96LRW14765) (PINUS ECHINATA POLLEN - UNII:96LRW14765)	PINUS ECHINATA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6748-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AMBROSIA ACANTHICARPA POLLEN 
false ragweed bur injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6749
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMBROSIA ACANTHICARPA POLLEN (UNII: U2AI3H2J5Y) (AMBROSIA ACANTHICARPA POLLEN - UNII:U2AI3H2J5Y)	AMBROSIA ACANTHICARPA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6749-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AMBROSIA TENUIFOLIA POLLEN 
slender ragweed injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6750
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMBROSIA TENUIFOLIA POLLEN (UNII: 57W5SO585B) (AMBROSIA TENUIFOLIA POLLEN - UNII:57W5SO585B)	AMBROSIA TENUIFOLIA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6750-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AMBROSIA BIDENTATA POLLEN 
southern ragweed injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6751
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMBROSIA BIDENTATA POLLEN (UNII: M3S672G75O) (AMBROSIA BIDENTATA POLLEN - UNII:M3S672G75O)	AMBROSIA BIDENTATA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6751-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AMBROSIA PSILOSTACHYA POLLEN 
western ragweed injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6752
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMBROSIA PSILOSTACHYA POLLEN (UNII: RX18M46K8L) (AMBROSIA PSILOSTACHYA POLLEN - UNII:RX18M46K8L)	AMBROSIA PSILOSTACHYA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6752-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

LOLIUM PERENNE SSP MULTIFLORUM POLLEN 
italian rye grass injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6754
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LOLIUM MULTIFLORUM POLLEN (UNII: VJI0WKK736) (LOLIUM MULTIFLORUM POLLEN - UNII:VJI0WKK736)	LOLIUM MULTIFLORUM POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6754-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ARTEMISIA FRIGIDA POLLEN 
prairie sage injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6755
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARTEMISIA FRIGIDA POLLEN (UNII: 5AN5LR8L3F) (ARTEMISIA FRIGIDA POLLEN - UNII:5AN5LR8L3F)	ARTEMISIA FRIGIDA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6755-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

DISTICHLIS SPICATA POLLEN 
salt grass injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6757
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DISTICHLIS SPICATA POLLEN (UNII: GOA51670YV) (DISTICHLIS SPICATA POLLEN - UNII:GOA51670YV)	DISTICHLIS SPICATA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6757-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

HOLCUS LANATUS POLLEN 
velvet grass injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6760
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOLCUS LANATUS POLLEN (UNII: 70O1TP6H01) (HOLCUS LANATUS POLLEN - UNII:70O1TP6H01)	HOLCUS LANATUS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6760-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

JUGLANS NIGRA POLLEN 
california walnut black pollen injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6761
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (JUGLANS NIGRA POLLEN - UNII:1BV28146ZR)	JUGLANS NIGRA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6761-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

JUGLANS REGIA POLLEN 
english walnut pollen injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6762
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
JUGLANS REGIA POLLEN (UNII: ARW43087I1) (JUGLANS REGIA POLLEN - UNII:ARW43087I1)	JUGLANS REGIA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6762-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

TRITICUM AESTIVUM POLLEN 
wheat pollen injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6763
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRITICUM AESTIVUM POLLEN (UNII: F1KAH8374D) (TRITICUM AESTIVUM POLLEN - UNII:F1KAH8374D)	TRITICUM AESTIVUM POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6763-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ARTEMISIA ANNUA POLLEN 
common wormwood annual injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6764
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARTEMISIA ANNUA POLLEN (UNII: 36R82U4DL6) (ARTEMISIA ANNUA POLLEN - UNII:36R82U4DL6)	ARTEMISIA ANNUA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6764-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AMARANTHUS TUBERCULATUS POLLEN 
water hemp injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6771
Route of Administration	PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMARANTHUS TUBERCULATUS POLLEN (UNII: 92N6W6KO2G) (AMARANTHUS TUBERCULATUS POLLEN - UNII:92N6W6KO2G)	AMARANTHUS TUBERCULATUS POLLEN	0.025 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mL  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6771-06	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

HOUSE DUST 
house dust injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6001
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOUSE DUST (UNII: EYO007VX98) (HOUSE DUST - UNII:EYO007VX98)	HOUSE DUST	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6001-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965	06/30/2013

BOS TAURUS SKIN 
cattle epithelium injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6301
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BOS TAURUS SKIN (UNII: 7J12CD6O9L) (BOS TAURUS SKIN - UNII:7J12CD6O9L)	BOS TAURUS SKIN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6301-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

COTTON FIBER 
cotton linters injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6303
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COTTON FIBER (UNII: 70LDW53ROO) (COTTON FIBER - UNII:70LDW53ROO)	COTTON FIBER	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6303-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CANIS LUPUS FAMILIARIS SKIN 
dog epithelium injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6305
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CANIS LUPUS FAMILIARIS SKIN (UNII: X2W7CLE97T) (CANIS LUPUS FAMILIARIS SKIN - UNII:X2W7CLE97T)	CANIS LUPUS FAMILIARIS SKIN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6305-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CAVIA PORCELLUS SKIN 
guinea pig epithelium injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6308
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAVIA PORCELLUS SKIN (UNII: GM3H4U6QS8) (CAVIA PORCELLUS SKIN - UNII:GM3H4U6QS8)	CAVIA PORCELLUS SKIN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6308-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

EQUUS CABALLUS SKIN 
horse epithelium injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6310
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EQUUS CABALLUS SKIN (UNII: 88VZV9HGT4) (EQUUS CABALLUS SKIN - UNII:88VZV9HGT4)	EQUUS CABALLUS SKIN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6310-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

MUS MUSCULUS SKIN 
mouse epithelium injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6316
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MUS MUSCULUS SKIN (UNII: 390AN9GB09) (MUS MUSCULUS SKIN - UNII:390AN9GB09)	MUS MUSCULUS SKIN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6316-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

RABBIT 
rabbit epithelium injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6319
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RABBIT (UNII: O5V0F26RUW) (RABBIT - UNII:O5V0F26RUW)	RABBIT	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6319-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SOLENOPSIS INVICTA 
fire ant injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6401
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SOLENOPSIS INVICTA (UNII: 5O7CR4P444) (SOLENOPSIS INVICTA - UNII:5O7CR4P444)	SOLENOPSIS INVICTA	10 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6401-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PERIPLANETA AMERICANA 
american cockroach injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6402
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (PERIPLANETA AMERICANA - UNII:2RQ1L9N089)	PERIPLANETA AMERICANA	100 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6402-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BLATELLA GERMANICA 
german cockroach injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6407
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BLATTELLA GERMANICA (UNII: G9O67I0A8Q) (BLATTELLA GERMANICA - UNII:G9O67I0A8Q)	BLATTELLA GERMANICA	100 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6407-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ACREMONIUM STRICTUM 
acremonium cephalosporium injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6501
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACREMONIUM STRICTUM (UNII: 3F36V0451W) (ACREMONIUM STRICTUM - UNII:3F36V0451W)	ACREMONIUM STRICTUM	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6501-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ALTERNARIA TENUIS 
alternaria tenuis a alternata injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6503
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6503-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ASPERGILLUS FUMIGATUS 
aspergillus fumigatus injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6506
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48)	ASPERGILLUS FUMIGATUS	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6506-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ASPERGILLUS NIGER VAR NIGER 
aspergillus niger injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6508
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6508-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AUREOBASIDIUM PULLULANS VAR PULLULANS 
aureobasidium pullularia pullulans injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6511
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK)	AUREOBASIDIUM PULLULANS VAR. PULLUTANS	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6511-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BOTRYTIS CINEREA 
botrytis cinerea injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6513
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7)	BOTRYTIS CINEREA	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6513-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CANDIDA ALBICANS 
candida albicans injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6515
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC)	CANDIDA ALBICANS	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6515-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CHAETOMIUM GLOBOSUM 
chaetomium globosum injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6517
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A)	CHAETOMIUM GLOBOSUM	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6517-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CLADOSPORIUM CLADOSPORIOIDES 
cladosporium cladosporioides hormodendrum clad injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6519
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLADOSPORIUM CLADOSPORIOIDES (UNII: 4ZWY20GTGO) (CLADOSPORIUM CLADOSPORIOIDES - UNII:4ZWY20GTGO)	CLADOSPORIUM CLADOSPORIOIDES	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6519-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CLADOSPORIUM SPHAEROSPERMUM 
cladosporium sphaerospermum hormodendrum hordei injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6521
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R)	CLADOSPORIUM SPHAEROSPERMUM	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6521-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

COCHLIOBOLUS SATIVUS 
drechslera helminthosporium injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6525
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W)	COCHLIOBOLUS SATIVUS	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6525-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

EPICOCCUM NIGRUM 
epicoccum nigrum injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6528
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7)	EPICOCCUM NIGRUM	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6528-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

FUSARIUM OXYSPORUM VASINFECTUM 
fusarium spp injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6532
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
FUSARIUM OXYSPORUM VASINFECTUM (UNII: 6M98DC08TZ) (FUSARIUM OXYSPORUM VASINFECTUM - UNII:6M98DC08TZ)	FUSARIUM OXYSPORUM VASINFECTUM	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6532-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

HELMINTHOSPORIUM SOLANI 
helminthosporium solani spondylocladium injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6535
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HELMINTHOSPORIUM SOLANI (UNII: U6Z259H815) (HELMINTHOSPORIUM SOLANI - UNII:U6Z259H815)	HELMINTHOSPORIUM SOLANI	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6535-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

MUCOR PLUMBEUS 
helminthmucor spp injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6537
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E)	MUCOR PLUMBEUS	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6537-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

NEUROSPORA INTERMEDIA 
neurospora spp injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6539
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI)	NEUROSPORA INTERMEDIA	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6539-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PHOMA EXIGUA VAR EXIGUA 
phoma herbarum injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6544
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PHOMA EXIGUA VAR. EXIGUA (UNII: 8JAG41IE4M) (PHOMA EXIGUA VAR. EXIGUA - UNII:8JAG41IE4M)	PHOMA EXIGUA VAR. EXIGUA	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6544-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

RHIZOPUS ARRHIZUS VAR ARRHIZUS 
rhizopus spp injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6547
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHIZOPUS ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS - UNII:8476849N1Y)	RHIZOPUS ARRHIZUS	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6547-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

RHODOTORULA RUBRA 
rhodotorula rubra injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6549
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHODOTORULA RUBRA (UNII: 15W81V867R) (RHODOTORULA RUBRA - UNII:15W81V867R)	RHODOTORULA RUBRA	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6549-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

STEMPHYLIUM SOLANI 
stemphylium spp injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6555
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
STEMPHYLIUM SOLANI (UNII: 1IEK4UDP5M) (STEMPHYLIUM SOLANI - UNII:1IEK4UDP5M)	STEMPHYLIUM SOLANI	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6555-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

TRICHOPHYTON MENTAGROPHYTES 
trichophyton mentagrophytes injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6557
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV)	TRICHOPHYTON MENTAGROPHYTES	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6557-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SACCHAROMYCES CEREVISIAE 
yeast saccharomyces cerevisiae injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6560
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) (SACCHAROMYCES CEREVISIAE - UNII:978D8U419H)	SACCHAROMYCES CEREVISIAE	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6560-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ACACIA 
acacia injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6676
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACACIA (UNII: 5C5403N26O) (ACACIA - UNII:5C5403N26O)	ACACIA	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6676-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ALNUS INCANA SSP RUGOSA POLLEN 
white alder injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6678
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALNUS INCANA SUBSP. RUGOSA POLLEN (UNII: 605T96G8Y5) (ALNUS INCANA SUBSP. RUGOSA POLLEN - UNII:605T96G8Y5)	ALNUS INCANA SUBSP. RUGOSA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6678-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

FRAXINUS VELUTINA POLLEN 
arizona ash injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6679
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
FRAXINUS VELUTINA POLLEN (UNII: LJT6I6Z8FD) (FRAXINUS VELUTINA POLLEN - UNII:LJT6I6Z8FD)	FRAXINUS VELUTINA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6679-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

FRAXINUS AMERICANA POLLEN 
white ash injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6680
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q) (FRAXINUS AMERICANA POLLEN - UNII:G684LX721Q)	FRAXINUS AMERICANA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6680-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PASPALUM NOTATUM POLLEN 
bahia grass injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6682
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK) (PASPALUM NOTATUM POLLEN - UNII:V003SHB7VK)	PASPALUM NOTATUM POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6682-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

MORELLA CERIFERA POLLEN 
bayberry wax myrtle injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6683
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MORELLA CERIFERA POLLEN (UNII: LC8MEV9S89) (MORELLA CERIFERA POLLEN - UNII:LC8MEV9S89)	MORELLA CERIFERA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6683-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

FAGUS GRANDIFOLIA POLLEN 
beech injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6684
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
FAGUS GRANDIFOLIA POLLEN (UNII: 34X886W1H4) (FAGUS GRANDIFOLIA POLLEN - UNII:34X886W1H4)	FAGUS GRANDIFOLIA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6684-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BETULA LENTA POLLEN 
black birch injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6686
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BETULA LENTA POLLEN (UNII: JQ5HI5004M) (BETULA LENTA POLLEN - UNII:JQ5HI5004M)	BETULA LENTA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6686-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BETULA NIGRA POLLEN 
river birch red injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6687
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BETULA NIGRA POLLEN (UNII: 93963RFO1P) (BETULA NIGRA POLLEN - UNII:93963RFO1P)	BETULA NIGRA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6687-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BETULA LENTA POLLEN 
white birch injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6688
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BETULA LENTA POLLEN (UNII: JQ5HI5004M) (BETULA LENTA POLLEN - UNII:JQ5HI5004M)	BETULA LENTA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6688-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ACER NEGUNDO POLLEN 
box elder ash leaf maple injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6690
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACER NEGUNDO POLLEN (UNII: P6K070AR8V) (ACER NEGUNDO POLLEN - UNII:P6K070AR8V)	ACER NEGUNDO POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6690-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BROMUS INERMIS POLLEN 
brome grass injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6692
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BROMUS INERMIS POLLEN (UNII: 766QT72BK6) (BROMUS INERMIS POLLEN - UNII:766QT72BK6)	BROMUS INERMIS POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6692-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AMARANTHUS PALMERI POLLEN 
carelessweed injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6693
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMARANTHUS PALMERI POLLEN (UNII: 1GH3WV23KH) (AMARANTHUS PALMERI POLLEN - UNII:1GH3WV23KH)	AMARANTHUS PALMERI POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6693-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

JUNIPERUS ASHEI POLLEN 
mountain cedar injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6694
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
JUNIPERUS ASHEI POLLEN (UNII: 544F8MEY0Y) (JUNIPERUS ASHEI POLLEN - UNII:544F8MEY0Y)	JUNIPERUS ASHEI POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6694-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

JUNIPERUS VIRGINIANA POLLEN 
red cedar injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6695
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
JUNIPERUS VIRGINIANA POLLEN (UNII: PY0JA16R2G) (JUNIPERUS VIRGINIANA POLLEN - UNII:PY0JA16R2G)	JUNIPERUS VIRGINIANA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6695-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

XANTHIUM STRUMARIUM VAR CANADENSE POLLEN 
cocklebur injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6696
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN (UNII: 0ZK6G3W3BI) (XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN - UNII:0ZK6G3W3BI)	XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6696-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

POPULUS DELTOIDES POLLEN 
eastern cottonwood common injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6699
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POPULUS DELTOIDES POLLEN (UNII: 476DVV63WP) (POPULUS DELTOIDES POLLEN - UNII:476DVV63WP)	POPULUS DELTOIDES POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6699-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

POPULUS DELTOIDES SSP MONILIFERA POLLEN 
western cottonwood injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6702
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN (UNII: 5928LJ1441) (POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN - UNII:5928LJ1441)	POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6702-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CUPRESSUS ARIZONICA POLLEN 
arizona cypress injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6703
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CUPRESSUS ARIZONICA POLLEN (UNII: 232DMH0XVF) (CUPRESSUS ARIZONICA POLLEN - UNII:232DMH0XVF)	CUPRESSUS ARIZONICA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6703-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

RUMEX ACETOSELLA POLLEN 
sour dock sheep sorrel injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6704
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RUMEX ACETOSELLA POLLEN (UNII: N52MIQ81ZW) (RUMEX ACETOSELLA POLLEN - UNII:N52MIQ81ZW)	RUMEX ACETOSELLA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6704-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

RUMEX CRISPUS POLLEN 
yellow dock injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6705
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RUMEX CRISPUS POLLEN (UNII: V825XJG64G) (RUMEX CRISPUS POLLEN - UNII:V825XJG64G)	RUMEX CRISPUS POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6705-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

EUPATORIUM CAPILLIFOLIUM POLLEN 
dog fennel injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6707
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EUPATORIUM CAPILLIFOLIUM POLLEN (UNII: B67NF86HF0) (EUPATORIUM CAPILLIFOLIUM POLLEN - UNII:B67NF86HF0)	EUPATORIUM CAPILLIFOLIUM POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6707-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ULMUS AMERICANA POLLEN 
american elm injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6708
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ULMUS AMERICANA POLLEN (UNII: 89BAT511BD) (ULMUS AMERICANA POLLEN - UNII:89BAT511BD)	ULMUS AMERICANA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6708-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ULMUS PUMILA POLLEN 
chinese elm injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6711
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ULMUS PUMILA POLLEN (UNII: 030R993R8E) (ULMUS PUMILA POLLEN - UNII:030R993R8E)	ULMUS PUMILA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6711-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

EUCALYPTUS GLOBULUS POLLEN 
eucalyptus injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6713
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EUCALYPTUS GLOBULUS POLLEN (UNII: 7XW7TB10X9) (EUCALYPTUS GLOBULUS POLLEN - UNII:7XW7TB10X9)	EUCALYPTUS GLOBULUS POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6713-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CORYLUS AMERICANA POLLEN 
hazelnut pollen injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6715
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CORYLUS AMERICANA POLLEN (UNII: ZGS382Y3AV) (CORYLUS AMERICANA POLLEN - UNII:ZGS382Y3AV)	CORYLUS AMERICANA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6715-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CARYA OVATA POLLEN 
shagbark hickory injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6716
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CARYA OVATA POLLEN (UNII: 54UN9R2798) (CARYA OVATA POLLEN - UNII:54UN9R2798)	CARYA OVATA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6716-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SORGHUM HALEPENSE POLLEN 
johnson grass injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6717
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP) (SORGHUM HALEPENSE POLLEN - UNII:577VA5B4HP)	SORGHUM HALEPENSE POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6717-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

JUNIPERUS CALIFORNICA POLLEN 
western juniper injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6719
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
JUNIPERUS CALIFORNICA POLLEN (UNII: 0H1V4V5V9L) (JUNIPERUS CALIFORNICA POLLEN - UNII:0H1V4V5V9L)	JUNIPERUS CALIFORNICA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6719-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

KOCHIA SCOPARIA POLLEN 
kochia firebush injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6720
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BASSIA SCOPARIA POLLEN (UNII: 07A108ZKW5) (BASSIA SCOPARIA POLLEN - UNII:07A108ZKW5)	BASSIA SCOPARIA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6720-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CHENOPODIUM ALBUM POLLEN 
lambs quarters injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6721
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN) (CHENOPODIUM ALBUM POLLEN - UNII:098LKX5NCN)	CHENOPODIUM ALBUM POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6721-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ROBINIA PSEUDOACACIA POLLEN 
black locust injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6723
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ROBINIA PSEUDOACACIA POLLEN (UNII: 8003NOJ82F) (ROBINIA PSEUDOACACIA POLLEN - UNII:8003NOJ82F)	ROBINIA PSEUDOACACIA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6723-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ACER RUBRUM POLLEN 
red maple injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6724
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACER RUBRUM POLLEN (UNII: 700NK45C76) (ACER RUBRUM POLLEN - UNII:700NK45C76)	ACER RUBRUM POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6724-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ACER SACCHARUM POLLEN 
sugar maple injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6725
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACER SACCHARUM POLLEN (UNII: V38QUQ7861) (ACER SACCHARUM POLLEN - UNII:V38QUQ7861)	ACER SACCHARUM POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6725-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

IVA XANTHIFOLIA POLLEN 
burweed marshelder injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6726
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CYCLACHAENA XANTHIFOLIA POLLEN (UNII: V80TPZ0T6J) (CYCLACHAENA XANTHIFOLIA POLLEN - UNII:V80TPZ0T6J)	CYCLACHAENA XANTHIFOLIA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6726-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

IVA ANNUA VAR ANNUA POLLEN 
rough marshelder injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6727
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
IVA ANNUA POLLEN (UNII: Y2U5S5PF22) (IVA ANNUA POLLEN - UNII:Y2U5S5PF22)	IVA ANNUA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6727-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PROSOPIS JULIFLORA POLLEN 
mesquite injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6730
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PROSOPIS JULIFLORA POLLEN (UNII: 6EIJ3D04MR) (PROSOPIS JULIFLORA POLLEN - UNII:6EIJ3D04MR)	PROSOPIS JULIFLORA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6730-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ARTEMISIA VULGARIS POLLEN 
common mugwort injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6732
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARTEMISIA VULGARIS POLLEN (UNII: ANT994T71D) (ARTEMISIA VULGARIS POLLEN - UNII:ANT994T71D)	ARTEMISIA VULGARIS POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6732-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

MORUS RUBRA POLLEN 
red mulberry injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6734
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MORUS RUBRA POLLEN (UNII: 9LYI4RTZ52) (MORUS RUBRA POLLEN - UNII:9LYI4RTZ52)	MORUS RUBRA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6734-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

MORUS ALBA POLLEN 
white mulberry injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6735
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MORUS ALBA POLLEN (UNII: 3I9T68187H) (MORUS ALBA POLLEN - UNII:3I9T68187H)	MORUS ALBA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6735-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

QUERCUS AGRIFOLIA POLLEN 
california live oak coast injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6737
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
QUERCUS AGRIFOLIA POLLEN (UNII: VOT5MA71M7) (QUERCUS AGRIFOLIA POLLEN - UNII:VOT5MA71M7)	QUERCUS AGRIFOLIA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6737-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

QUERCUS RUBRA POLLEN 
red oak injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6738
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
QUERCUS RUBRA POLLEN (UNII: SVW19ET93C) (QUERCUS RUBRA POLLEN - UNII:SVW19ET93C)	QUERCUS RUBRA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6738-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

QUERCUS VIRGINIANA POLLEN 
virginia live oak injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6739
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
QUERCUS VIRGINIANA POLLEN (UNII: 8KDG09A4GO) (QUERCUS VIRGINIANA POLLEN - UNII:8KDG09A4GO)	QUERCUS VIRGINIANA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6739-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

QUERCUS ALBA POLLEN 
white oak injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6740
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK) (QUERCUS ALBA POLLEN - UNII:Z4Y9ZSV4KK)	QUERCUS ALBA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6740-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BETULA LENTA POLLEN 
white pine injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6772
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BETULA LENTA POLLEN (UNII: JQ5HI5004M) (BETULA LENTA POLLEN - UNII:JQ5HI5004M)	BETULA LENTA POLLEN	0.002 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6772-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

OLEA EUROPAEA POLLEN 
olive pollen injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6773
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OLEA EUROPAEA POLLEN (UNII: 43R41XZ627) (OLEA EUROPAEA POLLEN - UNII:43R41XZ627)	OLEA EUROPAEA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6773-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SYAGRUS ROMANZOFFIANA POLLEN 
queen palm coco palm injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6774
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SYAGRUS ROMANZOFFIANA POLLEN (UNII: 84ZOM591BB) (SYAGRUS ROMANZOFFIANA POLLEN - UNII:84ZOM591BB)	SYAGRUS ROMANZOFFIANA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6774-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CARYA ILLINOINENSIS POLLEN 
pecan pollen injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6775
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CARYA ILLINOINENSIS POLLEN (UNII: PYO4JR720Y) (CARYA ILLINOINENSIS POLLEN - UNII:PYO4JR720Y)	CARYA ILLINOINENSIS POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6775-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AMARANTHUS RETROFLEXUS POLLEN 
rough pigweed redroot injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6776
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW) (AMARANTHUS RETROFLEXUS POLLEN - UNII:73B14PX5FW)	AMARANTHUS RETROFLEXUS POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6776-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CASUARINA EQUISETIFOLIA POLLEN 
australian pine beefwood injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6777
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CASUARINA EQUISETIFOLIA POLLEN (UNII: OZJ4OE173N) (CASUARINA EQUISETIFOLIA POLLEN - UNII:OZJ4OE173N)	CASUARINA EQUISETIFOLIA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6777-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PLANTAGO LANCEOLATA POLLEN 
english plantain injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6778
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI) (PLANTAGO LANCEOLATA POLLEN - UNII:DO87T1U2CI)	PLANTAGO LANCEOLATA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6778-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

POPULUS ALBA POLLEN 
white poplar injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6779
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POPULUS ALBA POLLEN (UNII: VU8C8SB23P) (POPULUS ALBA POLLEN - UNII:VU8C8SB23P)	POPULUS ALBA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6779-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

LIGUSTRUM VULGARE POLLEN 
privet injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6780
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIGUSTRUM VULGARE POLLEN (UNII: Y3FRX92Z0E) (LIGUSTRUM VULGARE POLLEN - UNII:Y3FRX92Z0E)	LIGUSTRUM VULGARE POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6780-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AMBROSIA ACANTHICARPA POLLEN 
false ragweed bur injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6781
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMBROSIA ACANTHICARPA POLLEN (UNII: U2AI3H2J5Y) (AMBROSIA ACANTHICARPA POLLEN - UNII:U2AI3H2J5Y)	AMBROSIA ACANTHICARPA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6781-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AMBROSIA TRIFIDA POLLEN 
tall ragweed giant injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6782
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMBROSIA TRIFIDA POLLEN (UNII: KU1V1898XX) (AMBROSIA TRIFIDA POLLEN - UNII:KU1V1898XX)	AMBROSIA TRIFIDA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6782-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AMBROSIA PSILOSTACHYA POLLEN 
western ragweed injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6783
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMBROSIA PSILOSTACHYA POLLEN (UNII: RX18M46K8L) (AMBROSIA PSILOSTACHYA POLLEN - UNII:RX18M46K8L)	AMBROSIA PSILOSTACHYA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6783-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SALSOLA KALI POLLEN 
russian thistle injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6784
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALSOLA KALI POLLEN (UNII: 2MH135KC6G) (SALSOLA KALI POLLEN - UNII:2MH135KC6G)	SALSOLA KALI POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6784-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ARTEMISIA FRIGIDA POLLEN 
prairie sage injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6785
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARTEMISIA FRIGIDA POLLEN (UNII: 5AN5LR8L3F) (ARTEMISIA FRIGIDA POLLEN - UNII:5AN5LR8L3F)	ARTEMISIA FRIGIDA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6785-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ARTEMISIA TRIDENTATA POLLEN 
common sagebrush injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6786
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARTEMISIA TRIDENTATA POLLEN (UNII: YI19RB8YFD) (ARTEMISIA TRIDENTATA POLLEN - UNII:YI19RB8YFD)	ARTEMISIA TRIDENTATA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6786-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

LIQUIDAMBAR STYRACIFLUA POLLEN 
sweetgum non stock injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6787
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIQUIDAMBAR STYRACIFLUA POLLEN (UNII: 5Q246DS5BS) (LIQUIDAMBAR STYRACIFLUA POLLEN - UNII:5Q246DS5BS)	LIQUIDAMBAR STYRACIFLUA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6787-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PLATANUS OCCIDENTALIS POLLEN 
american sycamore injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6788
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PLATANUS OCCIDENTALIS POLLEN (UNII: E03U1K03LK) (PLATANUS OCCIDENTALIS POLLEN - UNII:E03U1K03LK)	PLATANUS OCCIDENTALIS POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6788-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

HOLCUS LANATUS POLLEN 
velvet grass injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6790
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOLCUS LANATUS POLLEN (UNII: 70O1TP6H01) (HOLCUS LANATUS POLLEN - UNII:70O1TP6H01)	HOLCUS LANATUS POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6790-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

JUGLANS NIGRA POLLEN 
walnut black pollen injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6791
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (JUGLANS NIGRA POLLEN - UNII:1BV28146ZR)	JUGLANS NIGRA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6791-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

JUGLANS NIGRA POLLEN 
california walnut black pollen injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6792
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (JUGLANS NIGRA POLLEN - UNII:1BV28146ZR)	JUGLANS NIGRA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6792-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

JUGLANS REGIA POLLEN 
english walnut pollen injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6793
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
JUGLANS REGIA POLLEN (UNII: ARW43087I1) (JUGLANS REGIA POLLEN - UNII:ARW43087I1)	JUGLANS REGIA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6793-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AMARANTHUS TUBERCULATUS POLLEN 
water hemp injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6794
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMARANTHUS TUBERCULATUS POLLEN (UNII: 92N6W6KO2G) (AMARANTHUS TUBERCULATUS POLLEN - UNII:92N6W6KO2G)	AMARANTHUS TUBERCULATUS POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6794-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

TRITICUM AESTIVUM POLLEN 
wheat pollen injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6795
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRITICUM AESTIVUM POLLEN (UNII: F1KAH8374D) (TRITICUM AESTIVUM POLLEN - UNII:F1KAH8374D)	TRITICUM AESTIVUM POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6795-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SALIX NIGRA POLLEN 
black willow injection, solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 0268-6796
Route of Administration	INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALIX NIGRA POLLEN (UNII: 6M2JIH93ZN) (SALIX NIGRA POLLEN - UNII:6M2JIH93ZN)	SALIX NIGRA POLLEN	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)	0.004 mL  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.009 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00275 g  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0268-6796-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

Labeler - ALK-Abello, Inc. (809998847)

Establishment
Name	Address	ID/FEI	Business Operations
Alk-abello, Inc.		809998847	MANUFACTURE(0268-6000, 0268-6100, 0268-6101, 0268-6102, 0268-6103, 0268-6104, 0268-6793, 0268-6794, 0268-6795, 0268-6796, 0268-6786, 0268-6787, 0268-6788, 0268-6790, 0268-6791, 0268-6792, 0268-6780, 0268-6781, 0268-6782, 0268-6783, 0268-6784, 0268-6785, 0268-6774, 0268-6775, 0268-6776, 0268-6777, 0268-6778, 0268-6779, 0268-6737, 0268-6738, 0268-6739, 0268-6740, 0268-6772, 0268-6773, 0268-6726, 0268-6727, 0268-6730, 0268-6732, 0268-6734, 0268-6735, 0268-6719, 0268-6720, 0268-6721, 0268-6723, 0268-6724, 0268-6725, 0268-6708, 0268-6711, 0268-6713, 0268-6715, 0268-6716, 0268-6717, 0268-6699, 0268-6702, 0268-6703, 0268-6704, 0268-6705, 0268-6707, 0268-6690, 0268-6692, 0268-6693, 0268-6694, 0268-6695, 0268-6696, 0268-6682, 0268-6683, 0268-6684, 0268-6686, 0268-6687, 0268-6688, 0268-6557, 0268-6560, 0268-6676, 0268-6678, 0268-6679, 0268-6680, 0268-6537, 0268-6539, 0268-6544, 0268-6547, 0268-6549, 0268-6555, 0268-6519, 0268-6521, 0268-6525, 0268-6528, 0268-6532, 0268-6535, 0268-6506, 0268-6508, 0268-6511, 0268-6513, 0268-6515, 0268-6517, 0268-6319, 0268-6401, 0268-6402, 0268-6407, 0268-6501, 0268-6503, 0268-6301, 0268-6303, 0268-6305, 0268-6308, 0268-6310, 0268-6316, 0268-6761, 0268-6762, 0268-6763, 0268-6764, 0268-6771, 0268-6001, 0268-6751, 0268-6752, 0268-6754, 0268-6755, 0268-6757, 0268-6760, 0268-6743, 0268-6744, 0268-6745, 0268-6748, 0268-6749, 0268-6750, 0268-6714, 0268-6722, 0268-6728, 0268-6731, 0268-6736, 0268-6741, 0268-6700, 0268-6701, 0268-6706, 0268-6709, 0268-6710, 0268-6712, 0268-6674, 0268-6677, 0268-6681, 0268-6689, 0268-6691, 0268-6697, 0268-6657, 0268-6658, 0268-6659, 0268-6670, 0268-6671, 0268-6672, 0268-6648, 0268-6649, 0268-6651, 0268-6652, 0268-6654, 0268-6656, 0268-6641, 0268-6642, 0268-6643, 0268-6644, 0268-6646, 0268-6647, 0268-6635, 0268-6636, 0268-6637, 0268-6638, 0268-6639, 0268-6640, 0268-6627, 0268-6629, 0268-6630, 0268-6631, 0268-6632, 0268-6634, 0268-6620, 0268-6621, 0268-6622, 0268-6623, 0268-6625, 0268-6626, 0268-6613, 0268-6614, 0268-6615, 0268-6616, 0268-6618, 0268-6619, 0268-6606, 0268-6607, 0268-6608, 0268-6609, 0268-6610, 0268-6612, 0268-6558, 0268-6600, 0268-6601, 0268-6602, 0268-6603, 0268-6605, 0268-6545, 0268-6548, 0268-6550, 0268-6552, 0268-6553, 0268-6556, 0268-6529, 0268-6533, 0268-6536, 0268-6538, 0268-6540, 0268-6543, 0268-6514, 0268-6516, 0268-6518, 0268-6520, 0268-6524, 0268-6526, 0268-6500, 0268-6502, 0268-6504, 0268-6507, 0268-6509, 0268-6512, 0268-6317, 0268-6318, 0268-6320, 0268-6400, 0268-6403, 0268-6405, 0268-6304, 0268-6306, 0268-6309, 0268-6311, 0268-6312, 0268-6314, 0268-6230, 0268-6231, 0268-6233, 0268-6234, 0268-6300, 0268-6302, 0268-6219, 0268-6220, 0268-6221, 0268-6224, 0268-6226, 0268-6229, 0268-6210, 0268-6212, 0268-6213, 0268-6214, 0268-6216, 0268-6218, 0268-6202, 0268-6203, 0268-6204, 0268-6205, 0268-6206, 0268-6208, 0268-6193, 0268-6195, 0268-6196, 0268-6197, 0268-6198, 0268-6200, 0268-6185, 0268-6186, 0268-6187, 0268-6189, 0268-6191, 0268-6192, 0268-6174, 0268-6177, 0268-6178, 0268-6180, 0268-6181, 0268-6183, 0268-6143, 0268-6146, 0268-6149, 0268-6170, 0268-6171, 0268-6173, 0268-6135, 0268-6136, 0268-6137, 0268-6138, 0268-6139, 0268-6141, 0268-6127, 0268-6128, 0268-6129, 0268-6130, 0268-6132, 0268-6133, 0268-6120, 0268-6121, 0268-6122, 0268-6123, 0268-6124, 0268-6125, 0268-6112, 0268-6113, 0268-6114, 0268-6115, 0268-6116, 0268-6118, 0268-6105, 0268-6106, 0268-6107, 0268-6108, 0268-6109, 0268-6110)