COTTONSEED injection CULTIVATED OAT POLLEN- avena sativa injection CURVULARIA- curvularia lunata injection CYPRESS, ARIZONA POLLEN- cupressus arizonica injection DANDELION POLLEN- taraxacum officinale injection DATE PALM POLLEN- phoenix dactylifera injection DES .......ction COCKLEBUR POLLEN- xanthium commune injection COCKROACH, AMERICAN- periplaneta americana injection COCKROACH, GERMAN- blattella germanica injection COMMON SAGE POLLEN- artemisia tridentata injection CORN POLLEN POLLEN- zea mays injection COTTON LINTERS injection

Cotton Linters by

Drug Labeling and Warnings

Cotton Linters by is a Other medication manufactured, distributed, or labeled by Allermed Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BOXED WARNING

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WARNINGS

This allergenic 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.
This allergenic extract is not directly interchangeable with other allergenic extracts. The initial dose must be based on skin testing as described in the dosage and administration section of this insert. Patients being switched from other types of extracts, such as alum precipitated extracts, should be started as though they were coming under treatment for the first time. Patients should be instructed to recognize adverse reaction symptoms and cautioned to contact the physician's office if reaction symptoms occur. As with all allergenic extracts, severe systemic reactions may occur. In certain individuals these systemic reactions may occur. In certain individuals these reactions may be life threatening. Patients should be observed for at least 20 minutes following treatment, and emergency measures as well as personnel trained in their use should be immediately available in the event of a life threatening reaction.
This product should not be injected intravenously (see Dosage and Administration). Refer also to the Warnings, Precautions, Adverse Reactions and Overdosage sections below.

DESCRIPTION

Allergenic extract contains the aqueous extractables from allergenic source material in extracting solution containing 0.25% sodium chloride, 0.125% sodium bicarbonate, and 50% glycerol. 0.4% phenol is added as a preservative. The weight by volume value shown on the label is a measurement of extract concentration, rather than extract potency. Extracts for which U.S. standards exist are labeled in allergy units, in addition to w/v strength.

CLINICAL PHARMACOLOGY

Positive skin tests with allergenic extract are the result of histamine release from mast cells sensitized with allergen specific IgE. The exact mechanisms by which immunotherapy relieves symptoms of allergy are still under investigation. Elevations in allergen-specific IgG antibodies and an increase in the activity of T suppressor lymphocytes appear to be some of the immunologic changes that occur from hyposensitization. 1,2,3

INDICATIONS AND USAGE

Allergenic extract may be used as a diagnostic skin test reagent in persons suspected of being sensitive to the allergenic source material from which the extract is made. Skin tests should be used in conjunction with a thorough allergic history to establish the relevance of a given allergen in the etiology of allergic disease. 4,5,6
Immunotherapy with allergenic extract is indicated in persons suffering from allergic rhinitis, bronchitis, conjunctivitis, urticaria and asthma. The therapeutic efficacy of allergenic extract has been proven in ragweed, grass, and mountain cedar pollinosis, cat-induced asthma and hypersensitivity to hymenoptera venoms. 7-12
Immunotherapy may be used along with or exclusive of antihistamines and other medications used to control allergic symptoms.

CONTRAINDICATIONS

Allergenic extract should not be administered to a non-allergic person. However, there are no absolute contraindications to the use of allergenic extract for treatment in appropriate individuals. Relative contraindications include: EXTREME SENSITIVITY TO AN ALLERGEN - Determined from the allergic history, or from previous anaphylaxis following skin testing or subcutaneous injection; AUTOIMMUNE DISEASE - Individuals with autoimmune disease may be at risk, due to the possibility of routine immunizations exacerbating symptoms of the underlying disease; PREGNANCY - In limited controlled studies of women receiving allergenic extract during conception and throughout all trimesters of pregnancy, no evidence was found that extract is harmful to the fetus or mother. However, because of the known pharmacologic action of histamine on uterine muscle, any treatment that might result in the release of significant amounts of this mediator should be avoided if possible 13. See Precaution #4; MYOCARDIAL INFARCTION - Patients who have experienced a recent myocardial infarction may not be able to tolerate immunotherapy. As in all of the above circumstances, the benefit to risk ration must be carefully evaluated; BLEEDING DIATHESIS - Patients with a bleeding tendency should not be tested or treated with allergenic extract, unless the physician responsible believes that such procedures are safe to perform.
Allergenic extract should be temporarily withheld from patients if any of the following conditions exist: (1) severe symptoms of hay fever and/or asthma; (2) infection or flu accompanied by fever; and (3) exposure to excessive amounts of clinically relevant allergens prior to skin testing or immunotherapy.

WARNINGS

The only approved method for determining hypersensitivity to Allermed Laboratories Allergenic Extracts is by diagnostic skin testing (See DOSAGE AND ADMINISTRATION — DIAGNOSIS).
Physicians who administer allergenic extract should have emergency medication and equipment available to treat anaphylaxis 14. See Precautions, Adverse Reactions and Overdosage below.
To reduce the risk of anaphylaxis, the following measures must be observed:

1. Concentrated extract must be diluted before use for intradermal skin testing and for beginning immunotherapy. It should never be injected intravenously during testing or treatment procedures.
2. Patients who are highly sensitive, determined from clinical findings and test results, may require that treatment start with a very weak concentration of extract, such as 1:10,000,000 v/v.
3. The dosage of fresh (new) extract given to a patient receiving maintenance injections must be reduced to one-fourth the amount given from the previous (old) lot (See Immunotherapy, last paragraph).
4. Patients who are transferred to standardized extract after previous treatment with unstandardized extract must be skin tested with serial dilutions, starting with a 1:100,000 v/v dilution of the standardized extract, to determine a safe, non-reacting starting dose.
5. Patients who are transferred to this extract after treatment with alum precipitated or other modified extract must re-start injections with the beginning recommended dose of this extract.

PRECAUTIONS

1. Extract should be stored at 2°C to 8°C since higher temperatures may adversely affect the stability of the product. Do not freeze.
2. After the needle is inserted subcutaneously, the plunger should be withdrawn slightly to check for the presence of blood in the syringe. If blood is observed, a new injection should be prepared and given at another site, observing the same precautions.
3. Treatment with beta-blocking drugs may make patients refractory to the usual dose of epinephrine, in the event epinephrine is required to control an adverse allergic reaction.
4. PREGNANCY CATEGORY C. Allergenic extract. Animal reproduction studies have not been conducted with allergenic extract. It is also not known whether allergenic extract can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Allergenic extract should be given to a pregnant woman only if clearly needed.
5. PATIENT INSTRUCTIONS: Patients should be instructed to remain in the physician's office for at least 20 minutes after skin testing and after each treatment injection, and immediately notify the physician if symptoms of a generalized reaction or shock occur.
6. CARCINOGENESIS, MUTAGENESIS, IMPAIRMENT OF FERTILITY: Long term studies have not been conducted with allergenic extracts to determine their potential for carcinogenesis, mutagenesis, and impairment of fertility.
7. LACTATION: Data are not available on the secretion of allergenic extract in human milk and it is not known what affect this might have on the nursing infant.
8. PEDIATRIC USE: The dose of allergenic extract recommended for children is the same as that used for adults, except in the injection of large doses of extract for treatment. In this case, the amount of extract given to a child may be modified so that the discomfort of the injection is minimized.

ADVERSE REACTIONS

Local Reactions: The occurrence of a hive 5 to 15 minutes after the subcutaneous injection of extract does not require a reduction in dosage. However, a local reaction with edema larger than 2 cm in diameter or swelling and redness that persist for several hours or longer indicates that too much extract has been given. Treatment should be altered as follows:

1. Additional injections should not be given until all evidence of the reaction has disappeared.
2. The next injection administered should be 50% of the last non-reacting dose or less, depending upon the size and severity of the local reaction.
3. Subsequent injections should be continued at the reduced dosage unless the physician responsible for treatment believes that it is safe to increase the dose, and that possible clinical improvement would result form the administration of a larger dose of extract.
   
   

Systemic Reactions:Systemic (generalized) reactions may range from a mild exacerbation of the patient's allergic symptoms to hives, anaphylactic shock, or even death from anaphylaxis. The reaction usually occurs 5 to 20 minutes after injection. As a rule, the more quickly a reaction develops, the more serious it is likely to become. Symptoms may include sneezing, coughing, itching, shortness of breath, abdominal cramps, vomiting, diarrhea, tachycardia, hypotension and respiratory failure in severe cases. The reaction is usually stopped by the subcutaneous injection of Epinephrine HCL 1:1,000 (See Overdosage below). The oral administration of antihistamines and the placement of a tourniquet proximal to the injection site are helpful adjuncts. In the event that additional measures are required, it may be necessary to treat the patient for BRONCHOSPASM with intravenous aminophylline, intravenous fluids and corticosteroids; for HYPOTENSION with vasopressors, volume repletion, isoproterenol and corticosteroids; for LARYNGEAL OBSTRUCTION with oxygen and tracheostomy and for CARDIAC ARREST with cardiopulmonary resuscitation and other appropriate measures.
Immunotherapy after anaphylaxis should be continued if the cause of the reaction can be identified and appropriate precautions taken to insure that a subsequent reaction does not occur.

OVERDOSAGE

A strong local reaction to the injection of extract may be treated with oral antihistamines and the local application of a cold compress. The dosage must be reduced and additional extract must not be given until all evidence of the reaction has disappeared.
A systemic reaction following the injection of extract must be treated immediately. Reported procedures include (Ref. #4, vol. 2, p. 888):

1. 0.01 mL/kg up to 0.2 mL of aqueous epinephrine HCL 1:1000 subcutaneously at the injection site of antigen.
2. 0.01 mL/kg up to 0.3 mL of aqueous epinephrine HCL 1:1000 subcutaneously at another site.
3. Diphenhydramine intravenously or intramuscularly, 1.25 mg/kg up to 50 mg.
4. Tourniquet above the injection site of antigen.

Specific reactions:

1. Brochospasm: intravenous aminophylline 4 mg/kg up to 500 mg given over 10 to 15 minutes, aqueous hydrocortisone 5 mg/kg up to 200 mg, oxygen.
2. Laryngeal edema: oxygen, intubation, tracheostomy.
3. Hypotension: vasopressors, fluids, corticosteroids.
4. Cardiac arrest: resuscitation, sodium bicarbonate, defibrillation, antiarrhythmia medications.

DOSAGE AND ADMINISTRATION

Diagnosis: Concentrated extract may be used for scratch or prick testing providing the patient is not extremely sensitive. In this case, the extract should be diluted 10 fold before a scratch or prick test is performed. Extract for intradermal testing must be used as follows:

a. Patients with a negative scratch or prick test: Patients who do not react who do not react to a valid scratch or prick test should be tested intradermally with 0.05 mL of a 1:1000 v/v dilution of the concentrate. If the test is negative, a second test should be performed with 0.05 mL of a 1:100 v/v dilution or concentrate.
b. Patients with positive scratch or prick tests: It is not advisable to perform an intradermal skin test if the patient has a positive scratch or prick test.
c. Patients tested only by the intradermal method: Patients suspected of being highly allergic should be tested with 0.05 mL of a 1:100,000 v/v dilution of the concentrate. A negative test should be followed by repeat tests using 10 fold stronger concentrations until the maximum dose of 0.05 mL of a 1:100 v/v dilution is reached.

Interpretation of Results
Scratch and Prick Test
A negative test shows only a slight red area at the site of scarification or prick penetration. Positive tests are scored as follows:

1+ Erythema with 5 mm wheal
2+ Erythema with a 5-10 mm wheal
3+ Erythema with a 10-15 mm wheal
4+ Erythema with a wheal 15 mm (or larger) with pseudopodia

Intradermal Test
A negative test shows no change in the appearance and size of the 5 mm wheal created by the I.D. injection of 0.05 mL of extract. Positive tests are scored as follows:

1+ Erythema 10-20 mm with a 5-10 mm wheal
2+ Erythema 20-30 mm with a 5-10 mm wheal
3+ Erythema 30-40 mm with a 10-15 mm wheal
4+ Erythema greater than 40 mm with a 15 mm wheal (or larger) with pseudopodia

Immunotherapy

Allergenic extract should be administered subcutaneously in the outer aspect of the upper arm using a sterile tuberculin syringe and needle. The skin should be cleaned with 70% alcohol and aseptic technique should be observed in removing the extract from the vial. Care must be taken to avoid injecting the extract into a blood vessel because of the risk of anaphylaxis.
Concentrated extract must be diluted before administration to new patients. A 1:100,000 v/v dilution of concentrate is usually satisfactory to start treatment. However, as a precaution against overdose, a skin test with the intended starting dose should be done to help evaluate the patient's sensitivity to the product. If the skin response is larger than 5 mm edema/15 mm erythema, the extract is too strong and must be diluted before it is given subcutaneously. The doses shown in the Dosage Schedule (Table 1) below are recommended unless the patient's skin test response and allergic history indicates that more dilute extract should be used.
Little is known about the required accumulated dosage of allergen that is needed to relieve symptoms. However, studies have shown that high dose immunotherapy is efficacious in the treatment of allergic rhinitis and asthma. For this reason, treatment with extract from Vial #5 is recommended, providing the patient can tolerate the extract without experiencing local or systemic reactions. Treatment with Vial #6 may be used for patients who have not had adverse reactions to extract in Vial #5 and who require more concentrated extract to control or relieve symptoms.
Patients who have received allergenic extract for maintenance therapy SHOULD NOT be given the same dose from a fresh vial of extract. IT IS ADVISABLE TO REDUCE THE DOSAGE OF FRESH EXTRACT TO ONE-FOURTH THE AMOUNT GIVEN FROM A PREVIOUS LOT OF EXTRACT MADE AT THE SAME CONCENTRATION AND BY THE SAME FORMULA.

Table 1 - Suggested Dosage Schedule

No.	Vial #1 1:100,000 w/v frequency twice weekly mL	Vial #2 1:10,000 w/v frequency twice weekly mL	Vial #3 1:1,000 w/v frequency once weekly mL	Vial #4 1:100 w/v frequency once weekly mL	Vial #5 1:10 w/v frequency every two-four weeks mL	Vial #6 Concentrate frequency every two-four weeks mL
1	0.025	0.025	0.025	0.025	0.025	0.025
2	0.05	0.05	0.05	0.05	0.05	0.05
3	0.10	0.10	0.10	0.10	0.10	0.10
4	0.15	0.15	0.15	0.15	0.15	0.15
5	0.20	0.20	0.20	0.20	0.20	0.20
6	0.25	0.25	0.25	0.25	0.25	0.25
7	0.30	0.30	0.30	0.30	0.30	0.30

SUPPLIED

Allergenic extract is supplied in dropper vials for scratch or prick testing and in 10, 30, and 50 mL vials for bulk use.

WARRANTY

Allermed Laboratories, Inc. certifies that allergenic extract prepared within the Laboratories meets the safety and sterility standards of the F.D.A. Because the Laboratories have no control over the conditions under which extract is sued, or the purposes intended, neither a good nor a bad effect following its administration is warranted.
The users of this product should be aware of the potential dangers involved in the injection of allergenic extract and accept the risk of any consequences resulting from such injections.
No representatives of the Laboratories may change this warranty whether written, oral or implied. The buyer or user must assume full responsibility for the product after it leaves the premises of the Laboratories.

REFERENCES

1. Levy, D.A., L.M., Lichtenstein, E.O. Goldstein and K. Ishizaka. Immunologic and cellular changes accompanying the therapy of pollen allergy. J. Clinical Investigations. 50:360, 1971.
2. Evans, R., H. Pence, H. Kaplan and R. Rocklin. The effect of immunotherapy on humoral and cellular response in ragweed hayfever. J. Clinical Investigations. 57:1378, 1976.
3. Ishizaka, K. Cellular events in the IgE antibody response. Adv. In Immunology. 23:50, 1976.
4. Middleton, Elliott, Jr., C.E. Reed and E.F. Ellis (Eds.) Allergy, Principles and Practice Vols. 1&2, C.V. Mosby 1978.
5. Sheldon, J.M., R.G. Lovell and K.P. Matthews. A Manual of Clinical Allergy. W.B. Saunders, 1967.
6. Nelson, H.S. Diagnostic procedures in allergy. I. Allergy skin testing. Ann. Allergy. 51:411, 1983.
7. Norma, P.S., W.L. Winkenwerder and L.M. Lichtenstein. Immunotherapy of hay fever with ragweed antigen E: comparisons with whole pollen extract and placebos. J. Allergy. 42:93, 1968.
8. Milner, F.H. and E.C. Tees. Specific sensitivity to individual grass pollens in some hay fever patients. Clinical Allergy. 2:83, 1972.
9. Frankland, A.W. and R. Augustine. Grass pollen antigens effective in treatment. Clinical Science. 23:95, 1962.
10. Pence, H.L., D.Q. Mitchell, R.L. Greely, B.R. Updegraff and H.A. Selfridge. Immunotherapy for mountain cedar pollinosis: a double-blind controlled study. J. Allergy ad Clinical Immunology. 58:39, 1976.
11. Taylor, W.W., J.L. Ohman, Jr. and F.C. Lowell. Immunotherapy in cat-induced asthma. Double-blind trial with evaluation of bronchial responses to cat allergen and histamine. J. Allergy and Clinical Immunology. 61:283. 1978.
12. Lichtenstein, L.M., M.D. Valentine and A.K. Sobotka. Insect allergies. The state of the art. J. Allergy and Clinical Immunology. 61:268, 1978.
13. Metzger, W.J., E. Turner and R. Patterson. The safety of immunotherapy during pregnancy. J. Allergy and Clinical Immunology. 61:268. 1978.
14. Ouellette, J.J. Emergency management of allergic reactions. Modern Medicine 99, 1975.

Container Label

INGREDIENTS AND APPEARANCE

COTTONSEED 
cottonseed injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-005
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COTTON SEED (UNII: DI0ZRJ0MXN) (COTTON SEED - UNII:DI0ZRJ0MXN)	COTTON SEED	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-005-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-005-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-005-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-005-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

CULTIVATED OAT POLLEN 
avena sativa injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-322
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVENA SATIVA POLLEN (UNII: A7IKY24TR7) (AVENA SATIVA POLLEN - UNII:A7IKY24TR7)	AVENA SATIVA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-322-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-322-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-322-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-322-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

CURVULARIA 
curvularia lunata injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-109
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COCHLIOBOLUS LUNATUS (UNII: 4T82EA86AJ) (COCHLIOBOLUS LUNATUS - UNII:4T82EA86AJ)	COCHLIOBOLUS LUNATUS	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-109-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-109-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-109-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-109-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

CYPRESS, ARIZONA POLLEN 
cupressus arizonica injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-341
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-341-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-341-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-341-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-341-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

DANDELION POLLEN 
taraxacum officinale injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-416
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TARAXACUM OFFICINALE POLLEN (UNII: WQ3S5294XY) (TARAXACUM OFFICINALE POLLEN - UNII:WQ3S5294XY)	TARAXACUM OFFICINALE POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-416-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-416-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-416-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-416-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

DATE PALM POLLEN 
phoenix dactylifera injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-387
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PHOENIX DACTYLIFERA POLLEN (UNII: 2FV55IRB5B) (PHOENIX DACTYLIFERA POLLEN - UNII:2FV55IRB5B)	PHOENIX DACTYLIFERA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-387-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-387-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-387-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-387-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

DESERT RAGWEED POLLEN 
ambrosia dumosa injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-355
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMBROSIA DUMOSA POLLEN (UNII: ZIO18VN6HJ) (AMBROSIA DUMOSA POLLEN - UNII:ZIO18VN6HJ)	AMBROSIA DUMOSA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-355-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-355-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-355-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-355-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

DOCK, YELLOW POLLEN 
rumex crispus injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-406
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-406-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-406-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-406-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-406-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

DOG HAIR 
dog hair injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-006
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CANIS LUPUS FAMILIARIS HAIR (UNII: 05S7L91ZTR) (CANIS LUPUS FAMILIARIS HAIR - UNII:05S7L91ZTR)	CANIS LUPUS FAMILIARIS HAIR	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-006-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-006-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-006-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-006-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

EASTERN COTTONWOOD POLLEN 
populus deltoides injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-395
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-395-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-395-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-395-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-395-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

EASTERN SYCAMORE POLLEN 
platanus occidentalis injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-391
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-391-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-391-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-391-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-391-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

EASTERN WHITE PINE POLLEN 
pinus strobus injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-388
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-388-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-388-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-388-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-388-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

ENGLISH PLANTAIN POLLEN 
plantago lanceolata injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-389
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-389-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-389-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-389-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-389-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

ENGLISH WALNUT POLLEN 
juglans regia injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-367
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-367-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-367-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-367-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-367-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

EPICOCCUM 
epicoccum nigrum injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-110
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7)	EPICOCCUM NIGRUM	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-110-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-110-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-110-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-110-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

EUCALYPTUS POLLEN 
eucalyptus globulus injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-347
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-347-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-347-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-347-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-347-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

EUROPEAN OLIVE POLLEN 
olea europea injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-383
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-383-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-383-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-383-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-383-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

FALSE RAGWEED POLLEN 
ambrosia acanthicarpa injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-351
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-351-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-351-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-351-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-351-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

FLAXSEED 
flaxseed injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-010
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
FLAX SEED (UNII: 4110YT348C) (FLAX SEED - UNII:4110YT348C)	FLAX SEED	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-010-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-010-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-010-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-010-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

FREMONT COTTONWOOD POLLEN 
populus fremontii injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-396
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-396-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-396-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-396-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-396-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

FUSARIUM 
fusarium solani injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-111
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HAEMATONECTRIA HAEMATOCOCCA (UNII: 7TLR512M4A) (HAEMATONECTRIA HAEMATOCOCCA - UNII:7TLR512M4A)	HAEMATONECTRIA HAEMATOCOCCA	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-111-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-111-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-111-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-111-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

GAMBELS OAK POLLEN 
quercus gambelii injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-404
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
QUERCUS GAMBELII POLLEN (UNII: 9HC15X34LX) (QUERCUS GAMBELII POLLEN - UNII:9HC15X34LX)	QUERCUS GAMBELII POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-404-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-404-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-404-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-404-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

GIANT RAGWEED POLLEN 
ambrosia trifida injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-317
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-317-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-317-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-317-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-317-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

GLYCEROL-SALINE CONTROL 
glycerol-saline diluent injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-818
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	0.53 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-818-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-818-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-818-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-818-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

GOAT EPITHELIA 
goat epithelia injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-011
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAPRA HIRCUS SKIN (UNII: JLG9853E2P) (CAPRA HIRCUS SKIN - UNII:JLG9853E2P)	CAPRA HIRCUS SKIN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-011-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-011-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-011-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-011-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

GRAMA GRASS POLLEN 
bouteloua spp. injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-326
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BOUTELOUA GRACILIS POLLEN (UNII: 2XO08315X1) (BOUTELOUA GRACILIS POLLEN - UNII:2XO08315X1)	BOUTELOUA GRACILIS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-326-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-326-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-326-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-326-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

GRAY (WHITE) BIRCH POLLEN 
betula populifolia injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-325
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BETULA POPULIFOLIA POLLEN (UNII: 23H70FYJ5U) (BETULA POPULIFOLIA POLLEN - UNII:23H70FYJ5U)	BETULA POPULIFOLIA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-325-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-325-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-325-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-325-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

GREASEWOOD POLLEN 
sarcobatus vermiculatus injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-411
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SARCOBATUS VERMICULATUS POLLEN (UNII: 6532U64A3X) (SARCOBATUS VERMICULATUS POLLEN - UNII:6532U64A3X)	SARCOBATUS VERMICULATUS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-411-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-411-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-411-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-411-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

GREEN ASH POLLEN 
fraxinus pennsylvanica injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-358
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
FRAXINUS PENNSYLVANICA POLLEN (UNII: 2WZG2G15WX) (FRAXINUS PENNSYLVANICA POLLEN - UNII:2WZG2G15WX)	FRAXINUS PENNSYLVANICA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-358-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-358-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-358-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-358-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

GUINEA PIG EPITHELIA 
guinea pig epithelia injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-012
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-012-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-012-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-012-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-012-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

HACKBERRY POLLEN 
celtis occidentalis injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-336
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-336-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-336-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-336-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-336-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

HAMSTER EPITHELIA 
hamster epithelia injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-013
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MESOCRICETUS AURATUS SKIN (UNII: 3K873H631W) (MESOCRICETUS AURATUS SKIN - UNII:3K873H631W)	MESOCRICETUS AURATUS SKIN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-013-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-013-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-013-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-013-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

HARD MAPLE POLLEN 
acer saccharum injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-452
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-452-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-452-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-452-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-452-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

HAZELNUT POLLEN 
corylus americana injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-340
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-340-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-340-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-340-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-340-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

HELMINTHOSPORIUM SATIVUM 
helminthosporium sativum injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-112
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W)	COCHLIOBOLUS SATIVUS	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-112-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-112-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-112-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-112-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

HOG EPITHELIA 
hog epithelia injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-014
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SUS SCROFA SKIN (UNII: 3EM4VW6TQN) (SUS SCROFA SKIN - UNII:3EM4VW6TQN)	SUS SCROFA SKIN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-014-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-014-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-014-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-014-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

HORSE EPITHELIA 
horse epithelia injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-015
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EQUUS CABALLUS SKIN (UNII: 88VZV9HGT4) (EQUUS CABALLUS SKIN - UNII:88VZV9HGT4)	EQUUS CABALLUS SKIN	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-015-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-015-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-015-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-015-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

HOUSE DUST 
house dust injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-008
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOUSE DUST (UNII: EYO007VX98) (HOUSE DUST - UNII:EYO007VX98)	HOUSE DUST	0.02 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-008-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-008-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-008-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-008-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

IODINE BUSH POLLEN 
allenrolfea occidentalis injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-311
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLENROLFEA OCCIDENTALIS POLLEN (UNII: 5W6JAI84OI) (ALLENROLFEA OCCIDENTALIS POLLEN - UNII:5W6JAI84OI)	ALLENROLFEA OCCIDENTALIS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-311-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-311-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-311-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-311-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

JOHNSON GRASS POLLEN 
sorghum halepense injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-413
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-413-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-413-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-413-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-413-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

JUTE 
jute injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-016
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CORCORUS CAPSULARIS FIBER (UNII: TVA75O7S63) (CORCORUS CAPSULARIS FIBER - UNII:TVA75O7S63)	CORCORUS CAPSULARIS FIBER	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-016-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-016-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-016-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-016-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

KAPOK 
kapok injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-017
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CEIBA PENTANDRA FIBER (UNII: 758Z9H9WV9) (CEIBA PENTANDRA FIBER - UNII:758Z9H9WV9)	CEIBA PENTANDRA FIBER	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-017-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-017-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-017-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-017-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

KARAYA GUM 
karaya gum injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-018
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
KARAYA GUM (UNII: 73W9IQY50Q) (KARAYA GUM - UNII:73W9IQY50Q)	KARAYA GUM	0.01 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-018-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-018-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-018-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-018-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

KOELERS GRASS POLLEN 
koeleria cristata injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-375
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
KOELERIA MACRANTHA POLLEN (UNII: IIC6H3WF6J) (KOELERIA MACRANTHA POLLEN - UNII:IIC6H3WF6J)	KOELERIA MACRANTHA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-375-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-375-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-375-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-375-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

LAMBS QUARTERS POLLEN 
chenopodium album injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-339
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-339-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-339-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-339-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-339-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

LENS SCALE POLLEN 
atriplex lentiformis injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-440
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ATRIPLEX LENTIFORMIS POLLEN (UNII: 86LWA5503I) (ATRIPLEX LENTIFORMIS POLLEN - UNII:86LWA5503I)	ATRIPLEX LENTIFORMIS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-440-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-440-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-440-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-440-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

LINDEN POLLEN 
tilia cordata injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-460
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TILIA CORDATA POLLEN (UNII: OCO1LJR5YN) (TILIA CORDATA POLLEN - UNII:OCO1LJR5YN)	TILIA CORDATA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-460-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-460-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-460-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-460-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

LOMBARD POPLAR POLLEN 
populus nigra injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-397
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POPULUS NIGRA POLLEN (UNII: 0MGE63QPFJ) (POPULUS NIGRA POLLEN - UNII:0MGE63QPFJ)	POPULUS NIGRA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-397-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-397-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-397-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-397-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

MELALEUCA POLLEN 
melaleuca leucadendron injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-380
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-380-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-380-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-380-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-380-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

MESQUITE POLLEN 
prosopis juliflora injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-400
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-400-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-400-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-400-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-400-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

MONILIA 
monilia sitophila injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-113
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHRYSONILIA SITOPHILA (UNII: 296FK85FY6) (CHRYSONILIA SITOPHILA - UNII:296FK85FY6)	CHRYSONILIA SITOPHILA	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-113-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-113-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-113-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-113-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

MOUNTAIN CEDAR POLLEN 
juniperus sabinoides injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-371
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-371-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-371-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-371-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-371-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

MOUSE EPITHELIA 
mouse epithelia injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-019
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MUS MUSCULUS SKIN (UNII: 390AN9GB09) (MUS MUSCULUS SKIN - UNII:390AN9GB09)	MUS MUSCULUS SKIN	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-019-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-019-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-019-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-019-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

MUCOR 
mucor racemosus injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-114
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MUCOR RACEMOSUS (UNII: 17RH99LQ7G) (MUCOR RACEMOSUS - UNII:17RH99LQ7G)	MUCOR RACEMOSUS	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-114-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-114-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-114-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-114-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

MUGWORT SAGE POLLEN 
artemisia vulgaris injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-321
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-321-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-321-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-321-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-321-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

MUSTARD POLLEN 
brassica campestris injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-327
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BRASSICA RAPA POLLEN (UNII: 85Z8OHV3K7) (BRASSICA RAPA POLLEN - UNII:85Z8OHV3K7)	BRASSICA RAPA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-327-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-327-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-327-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-327-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

NETTLE POLLEN 
urtica dioica injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-423
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
URTICA DIOICA POLLEN (UNII: DNB59M1NVU) (URTICA DIOICA POLLEN - UNII:DNB59M1NVU)	URTICA DIOICA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-423-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-423-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-423-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-423-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

ORRIS ROOT 
orris root injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-020
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
IRIS GERMANICA VAR. FLORENTINA ROOT (UNII: M30XO5X4XD) (IRIS GERMANICA VAR. FLORENTINA ROOT - UNII:M30XO5X4XD)	IRIS GERMANICA VAR. FLORENTINA ROOT	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-020-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-020-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-020-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-020-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

PALO VERDE POLLEN 
cercidium torreyana injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-338
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PARKINSONIA FLORIDA POLLEN (UNII: 57586C96ZL) (PARKINSONIA FLORIDA POLLEN - UNII:57586C96ZL)	PARKINSONIA FLORIDA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-338-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-338-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-338-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-338-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

PECAN POLLEN 
carya illinoinensis injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-444
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-444-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-444-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-444-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-444-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

PENICILLIUM 
penicillium chrysogenum injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-115
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-115-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-115-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-115-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-115-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

PEPPER TREE POLLEN 
schinus molle injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-412
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-412-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-412-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-412-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-412-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

PHOMA 
phoma betae injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-116
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PLEOSPORA BETAE (UNII: V58BK047ES) (PLEOSPORA BETAE - UNII:V58BK047ES)	PLEOSPORA BETAE	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-116-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-116-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-116-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-116-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

POVERTY WEED POLLEN 
iva axillaris injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-363
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
IVA AXILLARIS POLLEN (UNII: 13KFG30UBR) (IVA AXILLARIS POLLEN - UNII:13KFG30UBR)	IVA AXILLARIS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-363-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-363-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-363-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-363-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

PRIVET POLLEN 
ligustrum vulgare injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-376
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-376-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-376-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-376-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-376-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

PULLULARIA 
pullularia pullulans injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-117
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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	0.01 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-117-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-117-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-117-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-117-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

PUSSY WILLOW POLLEN 
salix discolor injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-407
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALIX DISCOLOR POLLEN (UNII: ER172J09FM) (SALIX DISCOLOR POLLEN - UNII:ER172J09FM)	SALIX DISCOLOR POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-407-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-407-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-407-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-407-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

QUACKGRASS POLLEN 
agropyron repens injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-307
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-307-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-307-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-307-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-307-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

RABBITBUSH POLLEN 
ambrosia deltoides injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-354
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMBROSIA DELTOIDEA POLLEN (UNII: O4AB4546TP) (AMBROSIA DELTOIDEA POLLEN - UNII:O4AB4546TP)	AMBROSIA DELTOIDEA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-354-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-354-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-354-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-354-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

RED ALDER POLLEN 
alnus rubra injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-435
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALNUS RUBRA POLLEN (UNII: Z0F2YK1B7H) (ALNUS RUBRA POLLEN - UNII:Z0F2YK1B7H)	ALNUS RUBRA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-435-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-435-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-435-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-435-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

RED CEDAR POLLEN 
juniperus virginiana injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-373
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-373-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-373-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-373-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-373-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

RED MAPLE POLLEN 
acer rubrum injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-434
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-434-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-434-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-434-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-434-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

RED MULBERRY POLLEN 
morus rubra injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-447
Route of Administration	SUBCUTANEOUS, INTRADERMAL, CUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-447-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-447-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-447-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-447-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

RED OAK POLLEN 
quercus rubra injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-450
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-450-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-450-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-450-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-450-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

REDROOT PIGWEED POLLEN 
amaranthus retroflexus injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-314
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-314-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-314-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-314-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-314-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

RHIZOPUS 
rhizopus oryzae injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-118
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHIZOPUS ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS - UNII:8476849N1Y)	RHIZOPUS ARRHIZUS	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-118-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-118-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-118-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-118-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

RIVER/RED BIRCH POLLEN 
betula nigra injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-443
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-443-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-443-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-443-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-443-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

ROCKY MTN. JUNIPER POLLEN 
juniperus scopulorum injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-372
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
JUNIPERUS SCOPULORUM POLLEN (UNII: 0G82TT8ZFY) (JUNIPERUS SCOPULORUM POLLEN - UNII:0G82TT8ZFY)	JUNIPERUS SCOPULORUM POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-372-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-372-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-372-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-372-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

ROUGH MARSHELDER POLLEN 
iva ciliata injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-364
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-364-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-364-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-364-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-364-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

RUSSIAN OLIVE POLLEN 
elaeagnus angustifolia injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-346
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ELAEAGNUS ANGUSTIFOLIA POLLEN (UNII: 68P4F4M6VD) (ELAEAGNUS ANGUSTIFOLIA POLLEN - UNII:68P4F4M6VD)	ELAEAGNUS ANGUSTIFOLIA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-346-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-346-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-346-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-346-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

RUSSIAN THISTLE POLLEN 
salsola kali injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-410
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-410-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-410-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-410-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-410-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

RUST, WHEAT 
puccinia striiformis injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-120
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PUCCINIA STRIIFORMIS VAR. STRIIFORMIS (UNII: 9NLW29GJAX) (PUCCINIA STRIIFORMIS VAR. STRIIFORMIS - UNII:9NLW29GJAX)	PUCCINIA STRIIFORMIS VAR. STRIIFORMIS	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-120-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-120-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-120-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-120-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

SALT CEDAR POLLEN 
tamarix gallica injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-415
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TAMARIX GALLICA POLLEN (UNII: 43IR7KR479) (TAMARIX GALLICA POLLEN - UNII:43IR7KR479)	TAMARIX GALLICA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-415-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-415-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-415-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-415-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

SALT GRASS POLLEN 
distichlis spicata injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-345
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-345-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-345-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-345-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-345-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

SANDBUR RAGWEED POLLEN 
ambrosia bipinnatifida injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-353
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMBROSIA CHAMISSONIS POLLEN (UNII: 2Z41EEQ491) (AMBROSIA CHAMISSONIS POLLEN - UNII:2Z41EEQ491)	AMBROSIA CHAMISSONIS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-353-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-353-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-353-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-353-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

SHAD SCALE POLLEN 
atriplex confertifolia injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-439
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ATRIPLEX CONFERTIFOLIA POLLEN (UNII: GG8WX068MX) (ATRIPLEX CONFERTIFOLIA POLLEN - UNII:GG8WX068MX)	ATRIPLEX CONFERTIFOLIA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-439-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-439-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-439-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-439-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

SHAGBARK HICKORY POLLEN 
carya ovata injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-332
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-332-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-332-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-332-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-332-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

SHEEP SORREL POLLEN 
rumex acetosella injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-405
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-405-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-405-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-405-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-405-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

SHORTLEAF PINE POLLEN 
pinus echinata injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-448
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-448-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-448-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-448-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-448-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

SILVER MAPLE POLLEN 
acer saccharinum injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-304
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACER SACCHARINUM POLLEN (UNII: 95447163DG) (ACER SACCHARINUM POLLEN - UNII:95447163DG)	ACER SACCHARINUM POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-304-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-304-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-304-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-304-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

SILVER RAGWEED POLLEN 
dicoria canescens injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-344
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DICORIA CANESCENS POLLEN (UNII: E9H4GR1NMP) (DICORIA CANESCENS POLLEN - UNII:E9H4GR1NMP)	DICORIA CANESCENS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-344-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-344-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-344-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-344-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

SISAL 
sisal injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-021
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AGAVE SISALANA FIBER (UNII: MRJ91HVV4H) (AGAVE SISALANA FIBER - UNII:MRJ91HVV4H)	AGAVE SISALANA FIBER	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-021-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-021-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-021-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-021-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

SLENDER RAGWEED POLLEN 
ambrosia tenuifolia injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-356
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-356-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-356-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-356-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-356-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

SMOOTH BROME POLLEN 
bromus inermis injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-328
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-328-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-328-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-328-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-328-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

SMUT, CORN 
ustilago maydis injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-122
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-122-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-122-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-122-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-122-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

SMUT, JOHNSON GRASS 
sphacelotheca cruenta injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-123
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SPORISORIUM CRUENTUM (UNII: GQM6LVU5V8) (SPORISORIUM CRUENTUM - UNII:GQM6LVU5V8)	SPORISORIUM CRUENTUM	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-123-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-123-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-123-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-123-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

SMUT, WHEAT 
tilletia caries (tritici) injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-124
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TILLETIA CARIES (UNII: C7000B9PQI) (TILLETIA CARIES - UNII:C7000B9PQI)	TILLETIA CARIES	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-124-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-124-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-124-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-124-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

SPRING BIRCH POLLEN 
betula fontinalis injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-441
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BETULA OCCIDENTALIS POLLEN (UNII: R889N2L976) (BETULA OCCIDENTALIS POLLEN - UNII:R889N2L976)	BETULA OCCIDENTALIS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-441-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-441-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-441-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-441-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

STEMPHYLIUM 
stemphylium botryosum injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-126
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PLEOSPORA TARDA (UNII: TPL549N9R8) (PLEOSPORA TARDA - UNII:TPL549N9R8)	PLEOSPORA TARDA	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-126-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-126-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-126-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-126-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

SUGAR BEET POLLEN 
beta vulgaris injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-324
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BETA VULGARIS POLLEN (UNII: W7NU4B5CIY) (BETA VULGARIS POLLEN - UNII:W7NU4B5CIY)	BETA VULGARIS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-324-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-324-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-324-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-324-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

SUNFLOWER POLLEN 
helianthus annua injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-360
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HELIANTHUS ANNUUS POLLEN (UNII: 28D6K7E9IP) (HELIANTHUS ANNUUS POLLEN - UNII:28D6K7E9IP)	HELIANTHUS ANNUUS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-360-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-360-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-360-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-360-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

SWEET GUM POLLEN 
liquidamber styraciflua injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-377
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-377-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-377-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-377-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-377-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

TAG ALDER POLLEN 
alnus rugosa injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-436
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-436-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-436-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-436-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-436-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

TOBACCO LEAF 
tobacco leaf injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-022
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOBACCO LEAF (UNII: 6YR2608RSU) (TOBACCO LEAF - UNII:6YR2608RSU)	TOBACCO LEAF	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-022-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-022-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-022-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-022-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

TREE OF HEAVEN POLLEN 
ailanthus altissima injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-310
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-310-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-310-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-310-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-310-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

UTAH JUNIPER POLLEN 
juniperus osteosperma injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-370
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
JUNIPERUS OSTEOSPERMA POLLEN (UNII: 15L060HV8H) (JUNIPERUS OSTEOSPERMA POLLEN - UNII:15L060HV8H)	JUNIPERUS OSTEOSPERMA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-370-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-370-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-370-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-370-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

VELVET GRASS POLLEN 
holcus lanatus injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-361
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-361-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-361-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-361-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-361-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

WESTERN JUNIPER POLLEN 
juniperus occidentalis injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-369
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
JUNIPERUS OCCIDENTALIS POLLEN (UNII: 7JWJ3HXZ9U) (JUNIPERUS OCCIDENTALIS POLLEN - UNII:7JWJ3HXZ9U)	JUNIPERUS OCCIDENTALIS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-369-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-369-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-369-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-369-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

WESTERN RAGWEED POLLEN 
ambrosia psilostachia injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-316
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-316-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-316-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-316-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-316-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

WESTERN SYCAMORE POLLEN 
platanus racemosa injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-392
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PLATANUS RACEMOSA POLLEN (UNII: BWC8DYU8OS) (PLATANUS RACEMOSA POLLEN - UNII:BWC8DYU8OS)	PLATANUS RACEMOSA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-392-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-392-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-392-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-392-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

WESTERN WATERHEMP POLLEN 
acnida tamariscina injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-305
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMARANTHUS TUBERCULATUS POLLEN (UNII: 92N6W6KO2G) (AMARANTHUS TUBERCULATUS POLLEN - UNII:92N6W6KO2G)	AMARANTHUS TUBERCULATUS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-305-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-305-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-305-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-305-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

WESTERN WHEATGRASS POLLEN 
agropyron smithii injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-308
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PASCOPYRUM SMITHII POLLEN (UNII: 6AU0ZD8T1O) (PASCOPYRUM SMITHII POLLEN - UNII:6AU0ZD8T1O)	PASCOPYRUM SMITHII POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-308-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-308-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-308-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-308-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

WHITE ASH POLLEN 
fraxinus americana injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-357
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-357-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-357-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-357-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-357-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

WHITE HICKORY POLLEN 
carya tomentosa injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-334
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CARYA ALBA POLLEN (UNII: G2A764T54B) (CARYA ALBA POLLEN - UNII:G2A764T54B)	CARYA ALBA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-334-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-334-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-334-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-334-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

WHITE MULBERY POLLEN 
morus alba injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-382
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-382-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-382-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-382-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-382-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

WHITE OAK POLLEN 
quercus alba injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-402
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-402-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-402-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-402-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-402-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

WHITE POPLAR POLLEN 
populus alba injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-394
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-394-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-394-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-394-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-394-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

WING SCALE POLLEN 
atriplex canescens injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-438
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ATRIPLEX CANESCENS POLLEN (UNII: 26U0BU8G83) (ATRIPLEX CANESCENS POLLEN - UNII:26U0BU8G83)	ATRIPLEX CANESCENS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-438-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-438-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-438-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-438-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

WINTERFAT POLLEN 
eurotia lanata injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-348
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
KRASCHENINNIKOVIA LANATA POLLEN (UNII: 0GTO5BR99M) (KRASCHENINNIKOVIA LANATA POLLEN - UNII:0GTO5BR99M)	KRASCHENINNIKOVIA LANATA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-348-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-348-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-348-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-348-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

WORMWOOD SAGE POLLEN 
artemisia absinthium injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-319
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARTEMISIA ABSINTHIUM POLLEN (UNII: 81GS97HVFO) (ARTEMISIA ABSINTHIUM POLLEN - UNII:81GS97HVFO)	ARTEMISIA ABSINTHIUM POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-319-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-319-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-319-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-319-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

YELLOW PINE POLLEN 
pinus ponderosa injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-449
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PINUS PONDEROSA POLLEN (UNII: 042SUA2DS9) (PINUS PONDEROSA POLLEN - UNII:042SUA2DS9)	PINUS PONDEROSA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-449-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-449-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-449-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-449-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

ACACIA POLLEN 
acacia spp. injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-301
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACACIA POLLEN (UNII: 43DDR2YDYZ) (ACACIA POLLEN - UNII:43DDR2YDYZ)	ACACIA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-301-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-301-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-301-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-301-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

WALNUT MIX 
walnut mix injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-544
Route of Administration	PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (JUGLANS NIGRA POLLEN - UNII:1BV28146ZR)	JUGLANS NIGRA POLLEN	0.0167 g  in 1 mL
JUGLANS REGIA POLLEN (UNII: ARW43087I1) (JUGLANS REGIA POLLEN - UNII:ARW43087I1)	JUGLANS REGIA POLLEN	0.0167 g  in 1 mL
JUGLANS CALIFORNICA POLLEN (UNII: 2147EPR64I) (JUGLANS CALIFORNICA POLLEN - UNII:2147EPR64I)	JUGLANS CALIFORNICA POLLEN	0.0167 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.5 g  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-544-01	1 mL in 1 VIAL; Type 0: Not a Combination Product
2	NDC: 49643-544-05	5 mL in 1 VIAL; Type 0: Not a Combination Product
3	NDC: 49643-544-10	10 mL in 1 VIAL; Type 0: Not a Combination Product
4	NDC: 49643-544-30	30 mL in 1 VIAL; Type 0: Not a Combination Product
5	NDC: 49643-544-50	50 mL in 1 VIAL; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

ALTERNARIA 
alternaria alternata injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-101
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-101-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-101-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-101-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-101-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

ALDER, WHITE POLLEN 
alnus rhombifolia injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-312
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALNUS RHOMBIFOLIA POLLEN (UNII: 7X8HL8GRTM) (ALNUS RHOMBIFOLIA POLLEN - UNII:7X8HL8GRTM)	ALNUS RHOMBIFOLIA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-312-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-312-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-312-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-312-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

ALFALFA POLLEN 
medicago sativa injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-300
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MEDICAGO SATIVA POLLEN (UNII: G515RAI9FY) (MEDICAGO SATIVA POLLEN - UNII:G515RAI9FY)	MEDICAGO SATIVA POLLEN	0.02 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-300-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-300-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-300-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-300-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

ALKALI BLITE POLLEN 
suaeda spp. injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-414
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SUAEDA NIGRA POLLEN (UNII: FZU040QDS7) (SUAEDA NIGRA POLLEN - UNII:FZU040QDS7)	SUAEDA NIGRA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-414-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-414-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-414-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-414-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

AMERICAN ELM POLLEN 
ulmus americana injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-417
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-417-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-417-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-417-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-417-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

ARIZONA ASH POLLEN 
fraxinus velutina injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-359
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
FRAXINUS VELUTINA POLLEN (UNII: LJT6I6Z8FD) (FRAXINUS VELUTINA POLLEN - UNII:LJT6I6Z8FD)	FRAXINUS VELUTINA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-359-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-359-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-359-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-359-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

ARROYO WILLOW POLLEN 
salix lasiolepsis injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-408
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALIX LASIOLEPIS POLLEN (UNII: 808UWJ59FI) (SALIX LASIOLEPIS POLLEN - UNII:808UWJ59FI)	SALIX LASIOLEPIS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-408-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-408-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-408-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-408-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

ASPEN POLLEN 
populus tremuloides injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-398
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-398-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-398-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-398-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-398-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

ASPERGILLUS FUMIGATUS 
aspergillus fumigatus injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-130
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48)	ASPERGILLUS FUMIGATUS	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-130-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-130-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-130-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-130-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

AUSTRALIAN PINE POLLEN 
casuarina equisetifoli injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-335
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-335-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-335-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-335-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-335-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

BAHIA GRASS POLLEN 
paspalum notatum injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-384
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-384-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-384-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-384-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-384-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

BASSIA POLLEN 
bassia hyssopifolia injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-323
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BASSIA HYSSOPIFOLIA POLLEN (UNII: 35487N1IC9) (BASSIA HYSSOPIFOLIA POLLEN - UNII:35487N1IC9)	BASSIA HYSSOPIFOLIA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-323-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-323-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-323-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-323-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

BEECH POLLEN 
fagus grandifolia injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-349
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-349-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-349-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-349-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-349-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

BLACK COTTONWOOD POLLEN 
populus trichocarpa injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-399
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POPULUS TRICHOCARPA POLLEN (UNII: H8QYU50Z2D) (POPULUS TRICHOCARPA POLLEN - UNII:H8QYU50Z2D)	POPULUS TRICHOCARPA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-399-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-399-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-399-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-399-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

BLACK OAK POLLEN 
quercus velutina injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-451
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
QUERCUS VELUTINA POLLEN (UNII: 294L626TT0) (QUERCUS VELUTINA POLLEN - UNII:294L626TT0)	QUERCUS VELUTINA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-451-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-451-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-451-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-451-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

BLACK WALNUT POLLEN 
juglans nigra injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-366
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-366-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-366-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-366-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-366-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

BLACK WILLOW POLLEN 
salix nigra injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-409
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALIX NIGRA POLLEN (UNII: 6M2JIH93ZN) (SALIX NIGRA POLLEN - UNII:6M2JIH93ZN)	SALIX NIGRA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-409-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-409-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-409-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-409-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

BOTRYTIS 
botrytis cinerea injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-104
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7)	BOTRYTIS CINEREA	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-104-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-104-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-104-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-104-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

BOTTLEBRUSH POLLEN 
callistemon citrinus injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-330
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CALLISTEMON CITRINUS POLLEN (UNII: 62OII98F1T) (CALLISTEMON CITRINUS POLLEN - UNII:62OII98F1T)	CALLISTEMON CITRINUS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-330-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-330-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-330-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-330-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

BOX ELDER MAPLE POLLEN 
acer negundo injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-303
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-303-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-303-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-303-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-303-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

BURNING BUSH POLLEN 
kochia scoparia injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-374
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-374-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-374-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-374-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-374-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

BURROBRUSH POLLEN 
hymenoclea salsola injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-362
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMBROSIA SALSOLA POLLEN (UNII: 662J7FTA7T) (AMBROSIA SALSOLA POLLEN - UNII:662J7FTA7T)	AMBROSIA SALSOLA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-362-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-362-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-362-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-362-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

BURWEED MARSHELDER POLLEN 
iva xanthifolia injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-365
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-365-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-365-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-365-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-365-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

CALIF. BLACK WALNUT POLLEN 
juglans californica injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-446
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
JUGLANS CALIFORNICA POLLEN (UNII: 2147EPR64I) (JUGLANS CALIFORNICA POLLEN - UNII:2147EPR64I)	JUGLANS CALIFORNICA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-446-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-446-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-446-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-446-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

CALIFORNIA JUNIPER POLLEN 
juniperus californica injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-368
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-368-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-368-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-368-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-368-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

CALIFORNIA SCRUB OAK POLLEN 
quercus dumosa injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-403
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
QUERCUS DUMOSA POLLEN (UNII: P5W45RU6E4) (QUERCUS DUMOSA POLLEN - UNII:P5W45RU6E4)	QUERCUS DUMOSA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-403-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-403-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-403-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-403-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

CANARY GRASS POLLEN 
phalaris arundinaceae injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-385
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PHALARIS ARUNDINACEA POLLEN (UNII: FAY1Y90VJ9) (PHALARIS ARUNDINACEA POLLEN - UNII:FAY1Y90VJ9)	PHALARIS ARUNDINACEA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-385-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-385-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-385-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-385-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

CANDIDA 
candida albicans injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-105
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC)	CANDIDA ALBICANS	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-105-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-105-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-105-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-105-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

CANYON RAGWEED POLLEN 
ambrosia ambrosioides injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-352
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMBROSIA AMBROSIOIDES POLLEN (UNII: 81214Y871U) (AMBROSIA AMBROSIOIDES POLLEN - UNII:81214Y871U)	AMBROSIA AMBROSIOIDES POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-352-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-352-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-352-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-352-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

CARELESS WEED POLLEN 
amaranthus palmerii injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-313
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMARANTHUS PALMERI POLLEN (UNII: 1GH3WV23KH) (AMARANTHUS PALMERI POLLEN - UNII:1GH3WV23KH)	AMARANTHUS PALMERI POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-313-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-313-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-313-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-313-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

CATTLE EPITHELIA 
cattle epithelia injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-003
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BOS TAURUS SKIN (UNII: 7J12CD6O9L) (BOS TAURUS SKIN - UNII:7J12CD6O9L)	BOS TAURUS SKIN	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-003-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-003-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-003-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-003-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

CEPHALOSPORIUM 
cephalosporium roseum injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-106
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CEPHALOSPORIUM ROSEUM (UNII: 1756J4PM8P) (CEPHALOSPORIUM ROSEUM - UNII:1756J4PM8P)	CEPHALOSPORIUM ROSEUM	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-106-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-106-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-106-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-106-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

CHAETOMIUM 
chaetomium globosum injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-107
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A)	CHAETOMIUM GLOBOSUM	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-107-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-107-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-107-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-107-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

CHEAT GRASS POLLEN 
bromus secalinus injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-329
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BROMUS SECALINUS POLLEN (UNII: Q4T1SJ3046) (BROMUS SECALINUS POLLEN - UNII:Q4T1SJ3046)	BROMUS SECALINUS POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-329-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-329-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-329-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-329-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

CHERRY BIRCH POLLEN 
betula lenta injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-442
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-442-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-442-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-442-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-442-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

CHINESE ELM POLLEN 
ulmus pumila injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-419
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-419-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-419-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-419-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-419-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

CLADOSPORIUM 
cladosporium herbarum injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-108
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLADOSPORIUM HERBARUM (UNII: O64JF11198) (CLADOSPORIUM HERBARUM - UNII:O64JF11198)	CLADOSPORIUM HERBARUM	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-108-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-108-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-108-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-108-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

COAST LIVE OAK POLLEN 
quercus agrifolia injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-401
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-401-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-401-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-401-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-401-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

COAST MAPLE POLLEN 
acer macrophyllum injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-302
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACER MACROPHYLLUM POLLEN (UNII: E4CG5Q55M1) (ACER MACROPHYLLUM POLLEN - UNII:E4CG5Q55M1)	ACER MACROPHYLLUM POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-302-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-302-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-302-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-302-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

COAST SAGE POLLEN 
artemisia californica injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-437
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARTEMISIA CALIFORNICA POLLEN (UNII: 1EDY616508) (ARTEMISIA CALIFORNICA POLLEN - UNII:1EDY616508)	ARTEMISIA CALIFORNICA POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-437-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-437-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-437-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-437-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

COCKLEBUR POLLEN 
xanthium commune injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-420
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
XANTHIUM STRUMARIUM POLLEN (UNII: 2QOF601J1M) (XANTHIUM STRUMARIUM POLLEN - UNII:2QOF601J1M)	XANTHIUM STRUMARIUM POLLEN	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-420-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-420-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-420-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-420-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

COCKROACH, AMERICAN 
periplaneta americana injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-047
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (PERIPLANETA AMERICANA - UNII:2RQ1L9N089)	PERIPLANETA AMERICANA	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-047-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-047-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-047-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-047-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

COCKROACH, GERMAN 
blattella germanica injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-048
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BLATTELLA GERMANICA (UNII: G9O67I0A8Q) (BLATTELLA GERMANICA - UNII:G9O67I0A8Q)	BLATTELLA GERMANICA	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-048-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-048-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-048-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-048-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

COMMON SAGE POLLEN 
artemisia tridentata injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-320
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-320-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-320-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-320-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-320-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

CORN POLLEN POLLEN 
zea mays injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-422
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

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
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-422-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-422-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-422-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-422-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

COTTON LINTERS 
cotton linters injection

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 49643-004
Route of Administration	INTRADERMAL, CUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COTTON FIBER (UNII: 70LDW53ROO) (COTTON FIBER - UNII:70LDW53ROO)	COTTON FIBER	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.0025 g  in 1 mL
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	0.00125 g  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.53 g  in 1 mL
PHENOL (UNII: 339NCG44TV)	0.004 g  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49643-004-05	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 49643-004-10	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 49643-004-30	30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
4	NDC: 49643-004-50	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA102211	03/12/1974

Labeler - Allermed Laboratories, Inc. (073364531)

Establishment
Name	Address	ID/FEI	Business Operations
Allermed Laboratories, Inc.		073364531	manufacture