EPIDERMOPHYTON FLOCCOSUM solution FUSARIUM MIX- gibberella fujikuroi and fusarium solani solution MUCOR MIX- mucor circinelloides f. lusitanicus and mucor plumbeus solution NEW STOCK FUNGI MIX- acremonium strictum, alternaria alternata, aspergillus niger, aureobasidium pullulans, bipolaris sorokiniana, botrytis cinerea, candida albicans, chaetomiu .......EREA solution RHODOTORULA MUCILAGINOSA solution CLADOSPORIUM HERBARUM solution PHYCOMYCETES MIX- mucor circinelloides f. lusitanicus and rhizopus stolonifer solution MICROSPORUM CANIS solution BERMUDA GRASS SMUT- ustilago cynodontis solution ASPERGILLUS AMSTELODAMI solution

Epidermophyton floccosum by

Drug Labeling and Warnings

Epidermophyton floccosum by is a Other medication manufactured, distributed, or labeled by Greer Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BOXED WARNING

(What is this?)

WARNING

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.

ALLERGENIC EXTRACTS MAY CAUSE SEVERE OR FATAL ANAPHYLAXIS IN EXTREMELY SENSITIVE PATIENTS. THE INITIAL DOSE MUST BE BASED ON SKIN TESTING AS DESCRIBED IN THE DOSAGE AND ADMINISTRATION SECTION OF THIS INSERT. PATIENTS SHOULD BE INSTRUCTED TO RECOGNIZE ADVERSE REACTION SYMPTOMS AND CAUTIONED TO CONTACT THE PHYSICIAN'S OFFICE IF REACTION SYMPTOMS OCCUR. IN CERTAIN INDIVIDUALS, THESE REACTIONS COULD BE FATAL. PATIENTS SHOULD BE OBSERVED FOR AT LEAST 20 MINUTES FOLLOWING TREATMENT.

EMERGENCY MEASURES, AS WELL AS PERSONNEL TRAINED IN THEIR USE, SHOULD BE IMMEDIATELY AVAILABLE IN THE EVENT OF A LIFE‑ THREATENING REACTION. PATIENTS BEING SWITCHED FROM ONE LOT OF EXTRACT TO ANOTHER FROM THE SAME MANUFACTURER SHOULD HAVE THEIR DOSE REDUCED BY 75%.

THIS PRODUCT SHOULD NOT BE INJECTED INTRAVENOUSLY.

REFER ALSO TO THE WARNINGS, PRECAUTIONS, ADVERSE REACTIONS AND OVERDOSAGE SECTION BELOW.

DESCRIPTION

Allergenic Extracts are supplied as a sterile solution for intracutaneous or subcutaneous administration. Concentrates contain the soluble extractants of the source material with 0.5% sodium chloride and 0.54% sodium bicarbonate at a pH of 6.8 to 8.4 as aqueous extracts in water for injection or in 50% glycerin. Aqueous extracts contain 0.4% phenol as a preservative and 50% glycerinated extracts contain 0.2% phenol. Diluted aqueous extracts contain Buffered Saline with 0.5% sodium chloride, 0.04% potassium phosphate, 0.11% sodium phosphate heptahydrate, and 0.4% phenol in water for injection.

Source materials for these extracts are as follows: Pollens are collected from the respective grasses, weeds, trees, shrubs, cultured plants and flowers. Mold extracts are produced from pure culture mycelial mats. Rusts and smuts are obtained from natural growths. Epidermal extracts are produced from the hide, hair, or feathers containing the natural dander, or from separated dander. Insects are the whole body insects. House dust is made from various dusts ordinarily found in the home with the extract dialyzed to remove low‑molecular weight irritants and concentrated to an extraction ratio of 1:1. Food extracts are prepared from the edible portions of the respective foods, obtained fresh if possible. Certain diagnostic food extracts contain 0.1% sodium formaldehyde sulfoxylate as an antioxidant. Other miscellaneous inhalants involved in respiratory allergy are obtained in the naturally occurring form to which a patient may be exposed.

Extracts are labeled either by weight‑to‑volume (w/v) based on the weight of the source material to the volume of the extracting fluid, or in protein nitrogen units (PNU) based on assay with one PNU representing 0.00001 mg of protein nitrogen.

CLINICAL PHARMACOLOGY

The allergic reaction is dependent upon the presence of antigen‑specific immunoglobulin E (IgE) antibodies that are bound to specific receptors on mast cells and basophils. The presence of IgE antibodies on mast cells and basophils sensitizes these cells and, upon interaction with the appropriate allergen, histamine and other mediators are released. IgE antibody has been shown to correlate with atopic diseases such as allergic rhinitis and allergic asthma. (1‑4) In the skin these mediators are responsible for the characteristic wheal and flare (erythema) reactions upon Allergenic Extract skin testing in persons with the specific allergies. (3‑7)

Specific immunotherapy with Allergenic Extracts as employed for over 45 years is helpful in reducing symptoms associated with exposure to the offending allergens. A summary of effectiveness by the Panel on Review of Allergenic Extracts, an advisory committee to the U.S. Food and Drug Administration, has been published. (8) Several mechanisms have been proposed to explain the effectiveness of immunotherapy: an increase in antigen‑specific IgG antibodies is frequently associated with clinical effectiveness, although correlation is not consistent in all studies; there is a decrease in specific IgE; and IgE production is suppressed during periods of seasonal or high exposure to the antigen. (9) Other changes following immunotherapy have been noted including development of auto‑anti‑idiotypic antibodies; a decrease in blood basophil sensitivity to allergen; a decrease in lymphokine production and lymphocyte proliferation by cells exposed to allergen; and development of allergen‑specific suppressor cells. (10) The complete mechanisms of immunotherapy are not known and remain the subject of investigation.

INDICATIONS & USAGE

Allergenic Extracts are indicated for the diagnosis and treatment of patients with immediate hypersensitivity allergy to the respective allergens, inhaled, ingested or otherwise introduced into contact with sensitive tissues. The diagnosis of IgE‑mediated allergy may be established by the allergy history, clinical evaluation, and skin test reactivity. (4,7,11) Immunotherapy with Allergenic Extracts is indicated when testing and patient history have identified the offending allergens and when it is not possible or practical to avoid these allergens. (12‑14) Food extracts have not been proven effective in immunotherapy.

The use of Allergenic Extracts for the above purposes should be made only by physicians with special familiarity and knowledge of allergy. (See DOSAGE AND ADMINISTRATION)

CONTRAINDICATIONS

There are no known absolute contraindications to the use of Allergenic Extracts for immunotherapy. Immunotherapy with specific antigens should not be done in those individuals who do not exhibit skin test or clinical sensitivity to the particular antigens. (See below under WARNINGS and PRECAUTIONS)

Allergenic extract injections should not be administered in the presence of diseases characterized by a bleeding diathesis.

Children with nephrotic syndrome require careful consideration and probably should not receive injection therapy because a variety of seemingly unrelated events, such as immunization, can cause an exacerbation of their nephrotic disease.

General contraindications include:

EXTREME SENSITIVITY TO THE SPECIFIC ALLERGEN ‑ Determined from previous anaphylaxis following exposure.

AUTOIMMUNE DISEASE ‑ Individuals with autoimmune disease may be at risk, due to the possibility of routine immunizations exacerbating symptoms of the underlying disease.

WARNINGS

Concentrated extracts must be diluted with a sterile diluent prior to first use on a patient for treatment or intradermal testing. Allergenic Extracts are manufactured to assure high potency and have the ability during skin testing and immunotherapy to cause serious local and systemic reactions including death in sensitive patients. Most reactions occur within 20 minutes after injection, (15) but may occur later. (16) To minimize the potential for local or systemic reactions, the relative sensitivity of the patient must be assessed from the allergic history and from clinical observations. Patients should be informed of these risks prior to skin testing and immunotherapy (see PRECAUTIONS and ADVERSE REACTIONS below).

Allergenic Extract immunotherapy doses should be lowered or temporarily withheld from patients if any of the following conditions exist:

(1) severe symptoms of rhinitis and/or asthma

(2) infection or flu accompanied by fever

(3) exposure to excessive amounts of clinically relevant allergen prior to a scheduled injection

(4) evidence of a local or systemic reaction to the preceding extract injection during a course of immunotherapy

The dosage must be reduced when modifying dosages or components in a mixture or an individual prescription, or when starting a patient on fresh extract, even though the labeled strength of the old and new vials may be the same. This reduction in dosage may be necessary due to the older vial losing potency during storage, or due to different sensitivities to different components. The amount of new extract given should not exceed 25% of the last dose given from the old vial, assuming both extracts contain comparable amounts of allergen. Any evidence of a local or generalized reaction requires a reduction in dosage during the initial stages of immunotherapy, as well as during maintenance therapy.

PRECAUTIONS

GENERAL:

Not for intravenous use!

Systemic allergic reactions may occur as a result of immunotherapy. The risk can be minimized by adherence to a careful injection schedule, which starts with a low concentration of extract and is increased slowly. Because of the danger of serious reactions, caution is needed in testing exquisitely sensitive patients, particularly with potent allergens, e.g., peanut, cottonseed, and flaxseed. (8) Such extracts should be appropriately diluted before use.

The physician must be prepared to treat anaphylaxis should it occur and have the necessary drugs and equipment on hand to do so. (17‑18) Extracts should not be administered by the patient or other individuals who are not prepared to treat anaphylaxis should it occur.

Patients receiving Allergenic Extracts should be kept under observation a minimum of twenty (20) minutes so that any adverse reaction can be observed and properly handled. (15) This time should be extended for high‑risk patients such as those with unstable asthma or those suffering an exacerbation of their symptoms.

Patients receiving beta blockers may not be responsive to beta adrenergic drugs used to treat anaphylaxis. The risks of anaphylaxis in these patients should be carefully weighed against the benefits of immunotherapy.

Check the lot number and dosage schedule of the patient to verify correctness of a prescription number, a vial number, or strength. Only after this verification has been made should an injection be given.

A separate sterile needle and syringe should be used for each patient to prevent transmission of hepatitis or other infectious agents.

INFORMATION FOR PATIENTS:

Most serious reactions following the administration of Allergenic Extracts occur within 20 minutes; the patient should remain under observation for this period of time or longer if instructed by the physician. The size of any local reaction should be recorded, because increasingly large local reactions may precede a subsequent systemic reaction with increasing dosage. The patient should be instructed to report any unusual reactions. In particular, this includes unusual swelling and/or tenderness at the injection site, or reactions such as rhinorrhea, sneezing, coughing, wheezing, shortness of breath, nausea, dizziness, or faintness. Reactions may occur some time after leaving the physician's office, in which case medical attention should be sought immediately.

DRUG INTERACTIONS: Skin test diagnosis with Allergenic Extracts is contraindicated within 24 hours after the last dose of most antihistamines, within 48 hours after the last dose of terfenadine, and within 3 weeks or longer after the last dose of astemizole. These products suppress histamine skin test reactions and could mask a positive response.

CARCINOGENESIS, MUTAGENESIS, IMPAIRMENT OF FERTILITY: There is no evidence of carcinogenicity, mutagenesis or impairment of fertility in humans from Allergenic Extracts. No long‑term studies in animals have been performed to evaluate carcinogenic potential.

PREGNANCY: PREGNANCY CATEGORY C ‑ Animal reproduction studies have not been conducted with Allergenic Extracts. It is also not known whether Allergenic Extracts can cause fetal harm when administered to a pregnant woman or whether they can affect reproduction capacity. Allergenic Extracts should be given to a pregnant woman only if clearly needed.

There is no evidence of adverse effects of Allergenic Extracts on the fetus. (8) Studies have not been performed in animals to determine whether extracts affect fertility in males or females, have teratogenic potential, or have other adverse effects on the fetus. Caution should be exercised in testing or treating pregnant females because a systemic reaction may cause an abortion as a result of uterine muscle contractions.

LABOR AND DELIVERY: There is no known information of adverse effects during labor and delivery.

NURSING MOTHERS: It is not known whether this product is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when extracts are administered to a nursing woman.

PEDIATRIC AND GERIATRIC USE: Although most extracts have not been studied systematically in children, children and geriatric patients appear to tolerate injections of Allergenic Extracts well. Studies with pollenosis and asthma have been conducted in children (e.g. refs. 19‑21). Extract usage in children should follow the same precautions as in adults.

ADVERSE REACTIONS

Adverse systemic reactions may occur within minutes upon use of an Allergenic Extract to which a person has specific sensitivity. These reactions consist primarily of allergic symptoms such as generalized skin erythema, urticaria, pruritus, angioedema, rhinitis, wheezing, laryngeal edema, and hypotension. Less commonly, nausea, emesis, abdominal cramps, diarrhea and uterine contractions may occur. Severe reactions may cause shock and loss of consciousness. Fatalities have occurred rarely. (8,22,23) These systemic reactions occur with varying frequency in different clinics and are usually less than 1%. To some extent, the reaction rate is related to the type and dose of administered extract and to the sensitivity of the patient. In general, immunotherapy with Allergenic Extracts is considered to be safe. (24) Despite all precautions, occasional reactions are unavoidable.

Adverse systemic reactions should be treated as follows:

A. A tourniquet should be immediately applied to the extremity above the site of injection. Release the tourniquet every few minutes for a few seconds.

B. Epinephrine 1:1000 should be injected immediately in the opposite arm in amounts of 0.3 to 0.5 mL and 0.2 mL epinephrine should be administered at the site of injection. For children below the age of 6 years, adjust the dosage of epinephrine to 0.005 mL per pound of body weight per dose. Repeat epinephrine dosage in 15 minutes if necessary and if symptoms persist.

C. Adverse reactions not responding to epinephrine therapy may require the use of parenteral bronchodilators, vasopressors, oxygen, or volume replacement therapy.

Local reactions consisting of erythema, itching, swelling, tenderness and sometimes pain may occur at the injection site. These reactions may appear within a few minutes to hours and persist for several days. Local cold applications and oral antihistamines may be effective treatment. For marked and prolonged local reactions, steroids may be helpful.

OVERDOSAGE

Systemic reactions are uncommon after injection, but if the patient receives more extract than can be tolerated at that particular time and begins to experience immediate hypersensitivity anaphylaxis, the procedures listed under ADVERSE REACTIONS should be instituted.

Overdosage may occur because of an error in the volume of extract injected, or an incorrect dilution injected, or because the patient may be exposed to airborne or environmental antigens simultaneously with injection of the same antigens. In the event of a systemic reaction occurring, the dosage schedule should be carefully adjusted as outlined above under WARNINGS.

DOSAGE & ADMINISTRATION

1. DIAGNOSTIC TESTING

For the patient with a suspected diagnosis of allergy to more than one antigen, initial skin testing should include the individual extracts. If a screening skin test with a mixture is used, a positive response should be followed by testing with the individual extracts to determine the degree of sensitivity to each and to guide in the selection of extracts and their concentration for immunotherapy if indicated. However, because a negative skin test with a mixture may not be indicative of the absence of allergy to one or more of the components due to their dilution, testing with individual extracts is more precise. False negative responses may occur if serum levels of antihistamines remain from prior medication administration (see CONTRAINDICATIONS). The use of a positive control is especially recommended for patients on prior medications which may decrease the histamine skin test response.

Scratch or Prick‑puncture Skin Testing:

Allergenic Extract concentrates may be used for scratch or prick‑puncture testing or scratch tests in 50% glycerin, 1:20 w/v or strongest available strength in 5 mL vials may be used. Prick‑puncture tests with concentrated extracts in patients highly sensitive to the specific antigen should yield distinctive wheals with diameters of greater than 5 mm and with much larger erythema reactions. Glycerinated histamine phosphate 5 mg/mL (1.8 mg/mL histamine base) or aqueous histamine phosphate 2.75 mg/mL (1 mg/mL histamine base; 1:1,000 W/V) may be used as a positive control.

Intradermal Skin Testing:

Extract for intradermal testing must be prepared by diluting the stock concentrate injection vials with sterile diluent (use normal or buffered saline, or normal saline with human serum albumin) or the appropriate dilutions may be purchased.

a. Patients with a negative scratch or prick‑puncture test:

Patients who do not react to a scratch or prick‑puncture test should be tested intradermally, using a 26 or 27 gauge 1/4 inch needle, with 0.02 to 0.05 mL of an appropriate extract dilution from 1/100 to 1/1000 of the concentrate. A negative test should be followed by a repeat test using a higher concentration until significant wheal and flare reaction sizes are attained or until the responses remain negative. As a negative control use the diluent or, in the case of extracts in 50% glycerin, use 0.5% to 1% glycerosaline solution. As a positive control, use glycerinated histamine phosphate diluted to 0.5 mg/mL (0.18 mg/mL histamine base) or aqueous histamine phosphate 0.275 mg/mL (0.1 mg/mL histamine base).

b. Patients tested only by the intradermal method:

Since highly reactive individuals may react intracutaneously at 1:1 million or even 1:10 million dilutions, any intradermal injection should be preceded by a puncture test and the dose adjusted accordingly. Other patients suspected of being moderately allergic should be tested with 0.02 to 0.05 mL of an appropriate extract dilution on the order of 1/10,000 to 1/100,000 of the concentrate. A negative test should be followed by repeat tests using progressively stronger ten‑fold concentrations until significant wheal and flare reaction sizes are attained, or until skin test responses with the higher concentrations remain negative. As a negative control, use the diluent or, in the case of extracts in 50% glycerin, use 0.5% to 1% glycerosaline solution. As a positive control, use glycerinated histamine phosphate diluted to 0.5 mg/mL (0.18 mg/mL histamine base) or aqueous histamine phosphate 0.275 mg/mL (0.1 mg/mL histamine base).

Skin tests are graded in terms of the wheal and erythema response noted at 15 to 20 minutes, and compared to the appropriate controls. Wheal and erythema sizes may be recorded by actual measurement.

2. IMMUNOTHERAPY

Immunotherapy is administered by subcutaneous injection. Dosage of Allergenic Extracts is individualized according to the patient's sensitivity, the clinical response, and tolerance to the extract administered during the phases of an injection regimen. The initial dose of the extract should be determined based on the puncture test reactivity. In patients who appear to be exquisitely sensitive by history and skin test, the initial dose of the extract should be 0.05 to 0.1 mL of a low concentration, such as dilution number 5 or 6 in below. Patients with lesser sensitivity may be started with 0.05 to 0.1 mL of the next higher concentration. The amount of Allergenic Extract is increased at each injection by no more than 50% of the previous amount, and the next increment is governed by the response to the last injection. Large local reactions which persist for longer than 24 hours are generally considered an indication for repeating the previous dose or reducing the dose at the next administration. Any evidence of systemic reaction is an indication for a reduction of 75% in the subsequent dose. The upper limits of dosage have not been established; however, doses larger than 0.2 mL of an extract in 50% glycerin may cause discomfort upon injection. The dosage of Allergenic Extract does not vary significantly with the allergic disease under treatment.

To prepare dilutions starting from a concentrate such as 1:10 W/V, 1:20 W/V, OR 20,000 PNU/mL, proceed as in Table 1 below. (Note: Add 0.5 mL of concentrate to 4.5 mL of sterile diluent and make additional dilutions in the same manner.)

TABLE 1

Ten-Fold Dilution Series *

* There is no direct potency correlation across the table between PNUs and W/V.
Dilution	Extract	Diluent	W/V	W/V	PNU/mL
0	Concentrate		1:10	1:20	20,000
1	0.5 mL in dilution concentrate	4.5 mL	1:100	1:200	2,000
2	0.5 mL in dilution 1	4.5 mL	1:1,000	1:2,000	200
3	0.5 mL in dilution 2	4.5 mL	1:10,000	1:20,000	20
4	0.5 mL in dilution 3	4.5 mL	1:100,000	1:200,000	2
5	0.5 mL in dilution 4	4.5 mL	1:1,000,000	1:2,000,000	0.2
6	0.5 mL in dilution 5	4.5 mL	1:10,000,000	1:20,000,000	0.0

HOW SUPPLIED

Stock concentrate extracts containing up to 40,000 PNU/mL, or 1:10 W/V or other dilutions as requested by the physician are supplied in 5, 10, 30 and 50 mL in aqueous or 50% glycerin buffered saline. House dust extract is supplied in a 1:1 W/V concentrate, or a maximum of 10,000 PNU/mL. Extracts are also supplied in dropper vials for scratch or prick testing.

STORAGE AND HANDLING

Allergenic Extracts should be stored at 2‑8°C and kept at this temperature range during office use. Refer to vial labels for expiration dates. Diluted extracts are inherently less stable than concentrates. Dilutions of glycerinated extracts which result in glycerin below 50% are also less stable. The more dilute extracts in aqueous diluents should be replenished daily. Potency of a particular dilution can be checked by skin test in comparison to a fresh dilution of the extract on an individual known to be allergic to the specific antigen.

REFERENCES

1. Lichtenstein LM, Ishizaka K, Norman PS, et al. IgE antibody measurements in ragweed hayfever: relationship to clinical severity and the results of immunotherapy. J Clin Invest 1973;52:474.
2. Elgefors B, Julin A, Johansson SGO. Immunoglobulin E in bronchial asthma. Acta Allergol 1974;29:327.
3. Norman PS. The clinical significance of IgE. Hosp Pract 1975;10:41‑49.
4. Bryant DA, Burns MW, Lazarus L. The correlation between skin tests, bronchial provocation tests and the serum level of IgE specific for common allergens in patients with asthma. Clin Allergy 1975;5:145.
5. Loeffler JA, Cawley LP, Moeder M. Serum IgE levels: correlation with skin test sensitivity. Ann Allergy 1973;31:331.
6. Pepys J. Skin tests in diagnosis. In Gell PGH, Coombs RRA, Lachman PJ, eds. Clinical aspects of Immunology. Oxford: Blackwell Scientific Publications, 1975.
7. Burrows B, et al. Respiratory disorders and allergy skin test reactions. Ann Allergy 1976;84:134.
8. Implementation of Efficacy Review, Allergenic Extracts. Federal Register 1985;50:3082‑3288
9. Levy DA, Lichenstein LM, Goldstein EO, Ishizaka K. Immunologic and cellular changes accompanying the therapy of pollen allergy. J Clin Invest 1973;50:360.
10. Gurka G, Rocklin R. Immunologic responses during allergen-specific immunotherapy for respiratory allergy. Ann Allergy 1988;61:239-43.
11. Zeiss CR Jr. Patient evaluation. In: Allergy and Clinical Immunology, Locky RF, ed. Garden City, N.Y.: Medical Examination Publishing 1976:616.
12. Frankland AW, Augustin R. Prophylaxis of summer hay‑fever and asthma: a controlled trial comparing crude grass‑pollen extracts with the isolated main protein component. Lancet 1954;1:1055.
13. Frankland AW, Augustin R. Grass pollen antigens effective in treatment. Clin Sci 1962;23:95.
14. Rohr AS, Marshall NA, Saxon A: Successful immunotherapy for Triatoma protracta‑induced anaphylaxis. J Allergy Clin Immunol 1984;73:369‑75.
15. Executive Committee, American Academy of Allergy and Immunology. The waiting period after allergen skin testing and immunotherapy (Position statement). J Allergy Clin Immunol 1990;85:526‑7.
16. Greenberg MA, Kaufman CR, Gonzalez GE, Rosenblatt CD, Smith LJ, Summers RJ. Late and immediate systemic‑allergic reactions to inhalant allergen immunotherapy. J Allergy Clin Immunol 1986;77:865‑70.
17. Ouellette JJ. Emergency management of the allergic reactions. Modern Medicine 1975;99.
18. Anderson JA, et al. Personnel and equipment to treat systemic reactions caused by immunotherapy with allergenic extracts. J Allergy Clin Immunol 1986;77:271‑3.
19. Sadan N, Rhyne MB, Mellits ED, et al. Immunotherapy of pollenosis in children: investigation of the immunologic basis of clinical improvement. N Eng J Med 1969;280:623.
20. Johnstone DE. Value of hyposensitization therapy for perennial bronchial asthma in children. Pediatrics 1961;27:39.
21. VanAsperin PP, Kemp AS, Mellis CM. Skin test reactivity and clinical allergen sensitivity in infancy. J Allergy Clin Immunol 1984;73:381‑6.
22. Committee on Safety of Medicine. Desensitizing vaccines. Br Med J 1986;293:948.
23. Lockey RF, Benedict LM, Turkeltaub PC, Bukantz SC. Fatalities from immunotherapy (IT) and skin testing (ST). J Allergy Clin Immunol 1987;79:660‑77.
24. Norman PS, Van Metre TE Jr. The safety of allergenic immunotherapy. J Allergy Clin Immunol 1990;85:522‑5.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EPIDERMOPHYTON FLOCCOSUM 
epidermophyton floccosum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1668
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EPIDERMOPHYTON FLOCCOSUM (UNII: 6JR6JTN25S) (EPIDERMOPHYTON FLOCCOSUM - UNII:6JR6JTN25S)	EPIDERMOPHYTON FLOCCOSUM	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1668-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

FUSARIUM MIX 
gibberella fujikuroi and fusarium solani solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9636
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HAEMATONECTRIA HAEMATOCOCCA (UNII: 7TLR512M4A) (HAEMATONECTRIA HAEMATOCOCCA - UNII:7TLR512M4A)	HAEMATONECTRIA HAEMATOCOCCA	0.025 g  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2)	GIBBERELLA FUJIKUROI	0.025 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9636-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9636-4	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	BLA101833	09/15/1981

FUSARIUM MIX 
gibberella fujikuroi and fusarium solani solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9637
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HAEMATONECTRIA HAEMATOCOCCA (UNII: 7TLR512M4A) (HAEMATONECTRIA HAEMATOCOCCA - UNII:7TLR512M4A)	HAEMATONECTRIA HAEMATOCOCCA	20000 [PNU]  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2)	GIBBERELLA FUJIKUROI	20000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9637-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9637-4	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	BLA101833	09/15/1981

FUSARIUM MIX 
gibberella fujikuroi and fusarium solani solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9638
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HAEMATONECTRIA HAEMATOCOCCA (UNII: 7TLR512M4A) (HAEMATONECTRIA HAEMATOCOCCA - UNII:7TLR512M4A)	HAEMATONECTRIA HAEMATOCOCCA	10000 [PNU]  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2)	GIBBERELLA FUJIKUROI	10000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9638-4	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	BLA101833	09/15/1981

FUSARIUM MIX 
gibberella fujikuroi and fusarium solani solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9639
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HAEMATONECTRIA HAEMATOCOCCA (UNII: 7TLR512M4A) (HAEMATONECTRIA HAEMATOCOCCA - UNII:7TLR512M4A)	HAEMATONECTRIA HAEMATOCOCCA	0.0005 g  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2)	GIBBERELLA FUJIKUROI	0.0005 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9639-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

FUSARIUM MIX 
gibberella fujikuroi and fusarium solani solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9641
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HAEMATONECTRIA HAEMATOCOCCA (UNII: 7TLR512M4A) (HAEMATONECTRIA HAEMATOCOCCA - UNII:7TLR512M4A)	HAEMATONECTRIA HAEMATOCOCCA	0.0125 g  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2)	GIBBERELLA FUJIKUROI	0.0125 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9641-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9641-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-9641-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

MUCOR MIX 
mucor circinelloides f. lusitanicus and mucor plumbeus solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9648
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MUCOR CIRCINELLOIDES F. LUSITANICUS (UNII: 0J0X819B3C) (MUCOR CIRCINELLOIDES F. LUSITANICUS - UNII:0J0X819B3C)	MUCOR CIRCINELLOIDES F. LUSITANICUS	0.025 g  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E)	MUCOR PLUMBEUS	0.025 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9648-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9648-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

NEW STOCK FUNGI MIX 
acremonium strictum, alternaria alternata, aspergillus niger, aureobasidium pullulans, bipolaris sorokiniana, botrytis cinerea, candida albicans, chaetomium globosum, cladosporium sphaerospermum, epicoccum nigrum, gibberella fujikuroi, mucor plumbeus, penicillium notatum, phoma betae, rhizopus stolonifer and trichophyton mentagrophytes solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9651
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PLEOSPORA BETAE (UNII: V58BK047ES) (PLEOSPORA BETAE - UNII:V58BK047ES)	PLEOSPORA BETAE	1250 [PNU]  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W)	COCHLIOBOLUS SATIVUS	1250 [PNU]  in 1 mL
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC)	CANDIDA ALBICANS	1250 [PNU]  in 1 mL
CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A)	CHAETOMIUM GLOBOSUM	1250 [PNU]  in 1 mL
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q)	RHIZOPUS STOLONIFER	1250 [PNU]  in 1 mL
TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV)	TRICHOPHYTON MENTAGROPHYTES	1250 [PNU]  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	1250 [PNU]  in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK)	AUREOBASIDIUM PULLULANS VAR. PULLUTANS	1250 [PNU]  in 1 mL
EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7)	EPICOCCUM NIGRUM	1250 [PNU]  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2)	GIBBERELLA FUJIKUROI	1250 [PNU]  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E)	MUCOR PLUMBEUS	1250 [PNU]  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	1250 [PNU]  in 1 mL
ACREMONIUM STRICTUM (UNII: 3F36V0451W) (ACREMONIUM STRICTUM - UNII:3F36V0451W)	ACREMONIUM STRICTUM	1250 [PNU]  in 1 mL
BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7)	BOTRYTIS CINEREA	1250 [PNU]  in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R)	CLADOSPORIUM SPHAEROSPERMUM	1250 [PNU]  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG)	PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM	1250 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9651-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9651-4	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	BLA101833	09/15/1981

MOLD MIX 2 
aureobasidium pullulans, curvularia spicifera, gibberella fujikuroi, mucor plumbeus and rhizopus stolonifer solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9610
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q)	RHIZOPUS STOLONIFER	8000 [PNU]  in 1 mL
COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD)	COCHLIOBOLUS SPICIFER	8000 [PNU]  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2)	GIBBERELLA FUJIKUROI	8000 [PNU]  in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK)	AUREOBASIDIUM PULLULANS VAR. PULLUTANS	8000 [PNU]  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E)	MUCOR PLUMBEUS	8000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9610-4	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	BLA101833	09/15/1981

MOLD MIX 1 
alternaria alternata, aspergillus niger, bipolaris sorokiniana, cladosporium sphaerospermum and penicillium notatum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9603
Route of Administration	INTRADERMAL, PERCUTANEOUS, 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	0.01 g  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	0.01 g  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W)	COCHLIOBOLUS SATIVUS	0.01 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	0.01 g  in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R)	CLADOSPORIUM SPHAEROSPERMUM	0.01 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9603-4	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	BLA101833	09/15/1981

NEW STOCK FUNGI MIX 
acremonium strictum, alternaria alternata, aspergillus niger, aureobasidium pullulans, bipolaris sorokiniana, botrytis cinerea, candida albicans, chaetomium globosum, cladosporium sphaerospermum, epicoccum nigrum, gibberella fujikuroi, mucor plumbeus, penicillium notatum, phoma betae, rhizopus stolonifer and trichophyton mentagrophytes solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9678
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q)	RHIZOPUS STOLONIFER	2500 [PNU]  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W)	COCHLIOBOLUS SATIVUS	2500 [PNU]  in 1 mL
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC)	CANDIDA ALBICANS	2500 [PNU]  in 1 mL
CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A)	CHAETOMIUM GLOBOSUM	2500 [PNU]  in 1 mL
TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV)	TRICHOPHYTON MENTAGROPHYTES	2500 [PNU]  in 1 mL
EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7)	EPICOCCUM NIGRUM	2500 [PNU]  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	2500 [PNU]  in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK)	AUREOBASIDIUM PULLULANS VAR. PULLUTANS	2500 [PNU]  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2)	GIBBERELLA FUJIKUROI	2500 [PNU]  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E)	MUCOR PLUMBEUS	2500 [PNU]  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	2500 [PNU]  in 1 mL
ACREMONIUM STRICTUM (UNII: 3F36V0451W) (ACREMONIUM STRICTUM - UNII:3F36V0451W)	ACREMONIUM STRICTUM	2500 [PNU]  in 1 mL
BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7)	BOTRYTIS CINEREA	2500 [PNU]  in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R)	CLADOSPORIUM SPHAEROSPERMUM	2500 [PNU]  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG)	PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM	2500 [PNU]  in 1 mL
PLEOSPORA BETAE (UNII: V58BK047ES) (PLEOSPORA BETAE - UNII:V58BK047ES)	PLEOSPORA BETAE	2500 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9678-4	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	BLA101833	09/15/1981

RHIZOPUS MIX 
rhizopus stolonifer and rhizopus oryzae solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9680
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q)	RHIZOPUS STOLONIFER	10000 [PNU]  in 1 mL
RHIZOPUS ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS - UNII:8476849N1Y)	RHIZOPUS ARRHIZUS	10000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9680-4	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	BLA101833	09/15/1981

RHIZOPUS MIX 
rhizopus stolonifer and rhizopus oryzae solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9669
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q)	RHIZOPUS STOLONIFER	0.0125 g  in 1 mL
RHIZOPUS ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS - UNII:8476849N1Y)	RHIZOPUS ARRHIZUS	0.0125 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9669-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9669-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-9669-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

GLIOCLADIUM VIRIDE 
gliocladium viride solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1684
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLIOCLADIUM VIRIDE (UNII: 8Z8C642TPL) (GLIOCLADIUM VIRIDE - UNII:8Z8C642TPL)	GLIOCLADIUM VIRIDE	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1684-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

MOLD MIX 2 
aureobasidium pullulans, curvularia spicifera, gibberella fujikuroi, mucor plumbeus and rhizopus stolonifer solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9612
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q)	RHIZOPUS STOLONIFER	0.0002 g  in 1 mL
COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD)	COCHLIOBOLUS SPICIFER	0.0002 g  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2)	GIBBERELLA FUJIKUROI	0.0002 g  in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK)	AUREOBASIDIUM PULLULANS VAR. PULLUTANS	0.0002 g  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E)	MUCOR PLUMBEUS	0.0002 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9612-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

AHH MOLD MIX 
alternaria alternata, bipolaris sorokiniana and cladosporium sphaerospermum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9622
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R)	CLADOSPORIUM SPHAEROSPERMUM	0.00033 g  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W)	COCHLIOBOLUS SATIVUS	0.00033 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	0.00033 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9622-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

AHH MOLD MIX 
alternaria alternata, bipolaris sorokiniana and cladosporium sphaerospermum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9673
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R)	CLADOSPORIUM SPHAEROSPERMUM	13333.333 [PNU]  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W)	COCHLIOBOLUS SATIVUS	13333.333 [PNU]  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	13333.333 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9673-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

AHH MOLD MIX 
alternaria alternata, bipolaris sorokiniana and cladosporium sphaerospermum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9623
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R)	CLADOSPORIUM SPHAEROSPERMUM	0.0166 g  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W)	COCHLIOBOLUS SATIVUS	0.0166 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	0.0166 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9623-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9623-4	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	BLA101833	09/15/1981

AHH MOLD MIX 
alternaria alternata, bipolaris sorokiniana and cladosporium sphaerospermum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9621
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R)	CLADOSPORIUM SPHAEROSPERMUM	0.0166 g  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W)	COCHLIOBOLUS SATIVUS	0.0166 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	0.0166 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9621-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9621-4	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	BLA101833	09/15/1981

ALTERNARIA/HORMODENDRUM MIX 
alternaria alternata and aspergillus fumigatus solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9624
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48)	ASPERGILLUS FUMIGATUS	0.025 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	0.025 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9624-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

ASPERGILLUS MIX 
aspergillus amstelodami, aspergillus flavus, aspergillus fumigatus, aspergillus nidulans and aspergillus niger solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9630
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	0.01 g  in 1 mL
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48)	ASPERGILLUS FUMIGATUS	0.01 g  in 1 mL
EUROTIUM AMSTELODAMI (UNII: D932NLL87Z) (EUROTIUM AMSTELODAMI - UNII:D932NLL87Z)	EUROTIUM AMSTELODAMI	0.01 g  in 1 mL
ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13)	ASPERGILLUS FLAVUS	0.01 g  in 1 mL
ASPERGILLUS NIDULANS (UNII: 242A53RB80) (ASPERGILLUS NIDULANS - UNII:242A53RB80)	ASPERGILLUS NIDULANS	0.01 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9630-4	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	BLA101833	09/15/1981

DEMATIACEAE MIX 
alternaria alternata, aureobasidium pullulans, bipolaris sorokiniana, cladosporium herbarum, curvularia spicifera and helminthosporium solani solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9635
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD)	COCHLIOBOLUS SPICIFER	0.0042 g  in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK)	AUREOBASIDIUM PULLULANS VAR. PULLUTANS	0.0042 g  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W)	COCHLIOBOLUS SATIVUS	0.0042 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	0.0042 g  in 1 mL
CLADOSPORIUM HERBARUM (UNII: O64JF11198) (CLADOSPORIUM HERBARUM - UNII:O64JF11198)	CLADOSPORIUM HERBARUM	0.0042 g  in 1 mL
HELMINTHOSPORIUM SOLANI (UNII: U6Z259H815) (HELMINTHOSPORIUM SOLANI - UNII:U6Z259H815)	HELMINTHOSPORIUM SOLANI	0.0042 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9635-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9635-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

ASPERGILLUS NIDULANS 
aspergillus nidulans solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1623
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS NIDULANS (UNII: 242A53RB80) (ASPERGILLUS NIDULANS - UNII:242A53RB80)	ASPERGILLUS NIDULANS	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1623-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

ASPERGILLUS MIX 
aspergillus amstelodami, aspergillus flavus, aspergillus fumigatus, aspergillus nidulans and aspergillus niger solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9629
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	4000 [PNU]  in 1 mL
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48)	ASPERGILLUS FUMIGATUS	4000 [PNU]  in 1 mL
EUROTIUM AMSTELODAMI (UNII: D932NLL87Z) (EUROTIUM AMSTELODAMI - UNII:D932NLL87Z)	EUROTIUM AMSTELODAMI	4000 [PNU]  in 1 mL
ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13)	ASPERGILLUS FLAVUS	4000 [PNU]  in 1 mL
ASPERGILLUS NIDULANS (UNII: 242A53RB80) (ASPERGILLUS NIDULANS - UNII:242A53RB80)	ASPERGILLUS NIDULANS	4000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9629-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9629-4	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	BLA101833	09/15/1981

EPICOCCUM NIGRUM 
epicoccum nigrum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2665
Route of Administration	PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7)	EPICOCCUM NIGRUM	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2665-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

HELMINTHOSPORIUM SOLANI 
helminthosporium solani solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2668
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HELMINTHOSPORIUM SOLANI (UNII: U6Z259H815) (HELMINTHOSPORIUM SOLANI - UNII:U6Z259H815)	HELMINTHOSPORIUM SOLANI	20000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2668-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-2668-4	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	BLA101833	09/15/1981

HELMINTHOSPORIUM SOLANI 
helminthosporium solani solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5622
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HELMINTHOSPORIUM SOLANI (UNII: U6Z259H815) (HELMINTHOSPORIUM SOLANI - UNII:U6Z259H815)	HELMINTHOSPORIUM SOLANI	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5622-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5622-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-5622-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

MUCOR PLUMBEUS 
mucor plumbeus solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1694
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E)	MUCOR PLUMBEUS	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1694-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1694-4	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	BLA101833	09/15/1981

RHIZOPUS ORYZAE 
rhizopus oryzae solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5633
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHIZOPUS ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS - UNII:8476849N1Y)	RHIZOPUS ARRHIZUS	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5633-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

STEMPHYLIUM SOLANI 
stemphylium solani solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2637
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
STEMPHYLIUM SOLANI (UNII: 1IEK4UDP5M) (STEMPHYLIUM SOLANI - UNII:1IEK4UDP5M)	STEMPHYLIUM SOLANI	40000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2637-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-2637-4	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	BLA101833	09/15/1981

STEMPHYLIUM SOLANI 
stemphylium solani solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2636
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
STEMPHYLIUM SOLANI (UNII: 1IEK4UDP5M) (STEMPHYLIUM SOLANI - UNII:1IEK4UDP5M)	STEMPHYLIUM SOLANI	20000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2636-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

STEMPHYLIUM SOLANI 
stemphylium solani solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5637
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
STEMPHYLIUM SOLANI (UNII: 1IEK4UDP5M) (STEMPHYLIUM SOLANI - UNII:1IEK4UDP5M)	STEMPHYLIUM SOLANI	0.025 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5637-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2	NDC: 22840-5637-4	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	BLA101833	09/15/1981

TRICHODERMA HARZIANUM 
trichoderma harzianum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2642
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICHODERMA HARZIANUM (UNII: CA33Q4013Q) (TRICHODERMA HARZIANUM - UNII:CA33Q4013Q)	TRICHODERMA HARZIANUM	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2642-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

MUCOR CIRCINELLOIDES F. LUSITANICUS 
mucor circinelloides f. lusitanicus solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5625
Route of Administration	PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MUCOR CIRCINELLOIDES F. LUSITANICUS (UNII: 0J0X819B3C) (MUCOR CIRCINELLOIDES F. LUSITANICUS - UNII:0J0X819B3C)	MUCOR CIRCINELLOIDES F. LUSITANICUS	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5625-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

CHAETOMIUM GLOBOSUM 
chaetomium globosum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5612
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A)	CHAETOMIUM GLOBOSUM	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5612-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5612-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

CLADOSPORIUM SPHAEROSPERMUM 
cladosporium sphaerospermum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2663
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R)	CLADOSPORIUM SPHAEROSPERMUM	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2663-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

CLADOSPORIUM SPHAEROSPERMUM 
cladosporium sphaerospermum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5614
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R)	CLADOSPORIUM SPHAEROSPERMUM	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5614-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5614-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-5614-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

MUCOR CIRCINELLOIDES F. CIRCINELLOIDES 
mucor circinelloides f. circinelloides solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2669
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MUCOR CIRCINELLOIDES F. CIRCINELLOIDES (UNII: 48Z8OUT98B) (MUCOR CIRCINELLOIDES F. CIRCINELLOIDES - UNII:48Z8OUT98B)	MUCOR CIRCINELLOIDES F. CIRCINELLOIDES	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2669-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

ALTERNARIA/HORMODENDRUM MIX 
alternaria alternata and aspergillus fumigatus solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9625
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48)	ASPERGILLUS FUMIGATUS	0.0005 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	0.0005 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9625-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

MONILIA MIX 
candida albicans and neurospora intermedia solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9643
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC)	CANDIDA ALBICANS	500 [PNU]  in 1 mL
NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI)	NEUROSPORA INTERMEDIA	500 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9643-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

MONILIA MIX 
candida albicans and neurospora intermedia solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9677
Route of Administration	INTRADERMAL, PERCUTANEOUS, 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
NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI)	NEUROSPORA INTERMEDIA	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9677-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

MONILIA MIX 
candida albicans and neurospora intermedia solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9645
Route of Administration	PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC)	CANDIDA ALBICANS	0.025 g  in 1 mL
NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI)	NEUROSPORA INTERMEDIA	0.025 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9645-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9645-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-9645-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

MUCOR MIX 
mucor circinelloides f. lusitanicus and mucor plumbeus solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9646
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MUCOR CIRCINELLOIDES F. LUSITANICUS (UNII: 0J0X819B3C) (MUCOR CIRCINELLOIDES F. LUSITANICUS - UNII:0J0X819B3C)	MUCOR CIRCINELLOIDES F. LUSITANICUS	0.0005 g  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E)	MUCOR PLUMBEUS	0.0005 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9646-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

PENICILLIUM CHRYSOGENUM (NOTATUM) 
penicillium chrysogenum (notatum) solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5631
Route of Administration	PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL

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	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5631-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5631-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

TRICHODERMA HARZIANUM 
trichoderma harzianum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2640
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICHODERMA HARZIANUM (UNII: CA33Q4013Q) (TRICHODERMA HARZIANUM - UNII:CA33Q4013Q)	TRICHODERMA HARZIANUM	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2640-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-2640-4	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	BLA101833	09/15/1981

MOLD MIX 3 
alternaria alternata, aspergillus niger, cladosporium sphaerospermum and penicillium notatum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9616
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R)	CLADOSPORIUM SPHAEROSPERMUM	5000 [PNU]  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	5000 [PNU]  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	5000 [PNU]  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG)	PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM	5000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9616-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9616-4	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	BLA101833	09/15/1981

MOLD MIX 3 
alternaria alternata, aspergillus niger, cladosporium sphaerospermum and penicillium notatum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9617
Route of Administration	INTRADERMAL, SUBCUTANEOUS, PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R)	CLADOSPORIUM SPHAEROSPERMUM	0.025 g  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	0.025 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	0.025 g  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG)	PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM	0.025 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9617-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9617-4	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	BLA101833	09/15/1981

ALTERNARIA/HORMODENDRUM MIX 
alternaria alternata and aspergillus fumigatus solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9674
Route of Administration	INTRADERMAL, SUBCUTANEOUS, PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48)	ASPERGILLUS FUMIGATUS	10000 [PNU]  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	10000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9674-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9674-4	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	BLA101833	09/15/1981

ACREMONIUM STRICTUM 
acremonium strictum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5601
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SAROCLADIUM STRICTUM (UNII: 3F36V0451W) (SAROCLADIUM STRICTUM - UNII:3F36V0451W)	SAROCLADIUM STRICTUM	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5601-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5601-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

ASPERGILLUS NIGER 
aspergillus niger solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1627
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	20000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1627-4	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	BLA101833	09/15/1981

MOLD MIX 3 
alternaria alternata, aspergillus niger, cladosporium sphaerospermum and penicillium notatum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9619
Route of Administration	INTRADERMAL, SUBCUTANEOUS, PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R)	CLADOSPORIUM SPHAEROSPERMUM	0.0125 g  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	0.0125 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	0.0125 g  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG)	PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM	0.0125 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9619-4	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	BLA101833	09/15/1981

MONILIA MIX 
candida albicans and neurospora intermedia solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9642
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC)	CANDIDA ALBICANS	10000 [PNU]  in 1 mL
NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI)	NEUROSPORA INTERMEDIA	10000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9642-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9642-4	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	BLA101833	09/15/1981

NEW STOCK FUNGI MIX 
acremonium strictum, alternaria alternata, aspergillus niger, aureobasidium pullulans, bipolaris sorokiniana, botrytis cinerea, candida albicans, chaetomium globosum, cladosporium sphaerospermum, epicoccum nigrum, gibberella fujikuroi, mucor plumbeus, penicillium notatum, phoma betae, rhizopus stolonifer and trichophyton mentagrophytes solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9653
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q)	RHIZOPUS STOLONIFER	0.003125 g  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W)	COCHLIOBOLUS SATIVUS	0.003125 g  in 1 mL
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC)	CANDIDA ALBICANS	0.003125 g  in 1 mL
CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A)	CHAETOMIUM GLOBOSUM	0.003125 g  in 1 mL
TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV)	TRICHOPHYTON MENTAGROPHYTES	0.003125 g  in 1 mL
EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7)	EPICOCCUM NIGRUM	0.003125 g  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	0.003125 g  in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK)	AUREOBASIDIUM PULLULANS VAR. PULLUTANS	0.003125 g  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2)	GIBBERELLA FUJIKUROI	0.003125 g  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E)	MUCOR PLUMBEUS	0.003125 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	0.003125 g  in 1 mL
ACREMONIUM STRICTUM (UNII: 3F36V0451W) (ACREMONIUM STRICTUM - UNII:3F36V0451W)	ACREMONIUM STRICTUM	0.003125 g  in 1 mL
BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7)	BOTRYTIS CINEREA	0.003125 g  in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R)	CLADOSPORIUM SPHAEROSPERMUM	0.003125 g  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG)	PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM	0.003125 g  in 1 mL
PLEOSPORA BETAE (UNII: V58BK047ES) (PLEOSPORA BETAE - UNII:V58BK047ES)	PLEOSPORA BETAE	0.003125 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9653-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9653-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-9653-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

GRAIN SMUT MIX 
ustilago maydis, ustilago tritici, ustilago nuda and ustilago avenae solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9670
Route of Administration	PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
USTILAGO NUDA (UNII: 9Y53ZS6I82) (USTILAGO NUDA - UNII:9Y53ZS6I82)	USTILAGO NUDA	0.00625 g  in 1 mL
USTILAGO AVENAE (UNII: YIH315U1TU) (USTILAGO AVENAE - UNII:YIH315U1TU)	USTILAGO AVENAE	0.00625 g  in 1 mL
USTILAGO MAYDIS (UNII: 4K7Z7K7SWG) (USTILAGO MAYDIS - UNII:4K7Z7K7SWG)	USTILAGO MAYDIS	0.00625 g  in 1 mL
USTILAGO TRITICI (UNII: BV82OL2IZ8) (USTILAGO TRITICI - UNII:BV82OL2IZ8)	USTILAGO TRITICI	0.00625 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9670-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9670-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-9670-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

NEUROSPORA INTERMEDIA 
neurospora intermedia solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2600
Route of Administration	PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI)	NEUROSPORA INTERMEDIA	40000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2600-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-2600-4	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	BLA101833	09/15/1981

NEUROSPORA INTERMEDIA 
neurospora intermedia solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5627
Route of Administration	SUBCUTANEOUS, PERCUTANEOUS, INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI)	NEUROSPORA INTERMEDIA	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5627-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5627-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

PAECILOMYCES VARIOTII 
paecilomyces variotii solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2605
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PAECILOMYCES VARIOTII (UNII: KO7V58BY40) (PAECILOMYCES VARIOTII - UNII:KO7V58BY40)	PAECILOMYCES VARIOTII	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2605-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-2605-4	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	BLA101833	09/15/1981

PENICILLIUM DIGITATUM 
penicillium digitatum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5630
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PENICILLIUM DIGITATUM (UNII: 1SB49SV239) (PENICILLIUM DIGITATUM - UNII:1SB49SV239)	PENICILLIUM DIGITATUM	0.0125 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5630-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5630-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

PENICILLIUM CHRYSOGENUM (NOTATUM) 
penicillium chrysogenum (notatum) solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2615
Route of Administration	INTRADERMAL, PERCUTANEOUS, 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	40000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2615-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

PHOMA BETAE 
phoma betae solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5632
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PLEOSPORA BETAE (UNII: V58BK047ES) (PLEOSPORA BETAE - UNII:V58BK047ES)	PLEOSPORA BETAE	0.025 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5632-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5632-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

RHIZOPUS ORYZAE 
rhizopus oryzae solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2619
Route of Administration	INTRADERMAL, PERCUTANEOUS, 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 BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2619-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

ASPERGILLUS MIX 
aspergillus amstelodami, aspergillus flavus, aspergillus fumigatus, aspergillus nidulans and aspergillus niger solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9627
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	0.02 g  in 1 mL
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48)	ASPERGILLUS FUMIGATUS	0.02 g  in 1 mL
EUROTIUM AMSTELODAMI (UNII: D932NLL87Z) (EUROTIUM AMSTELODAMI - UNII:D932NLL87Z)	EUROTIUM AMSTELODAMI	0.02 g  in 1 mL
ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13)	ASPERGILLUS FLAVUS	0.02 g  in 1 mL
ASPERGILLUS NIDULANS (UNII: 242A53RB80) (ASPERGILLUS NIDULANS - UNII:242A53RB80)	ASPERGILLUS NIDULANS	0.02 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9627-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9627-4	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	BLA101833	09/15/1981

ALTERNARIA ALTERNATA 
alternaria alternata solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1604
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1604-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

ACREMONIUM STRICTUM 
acremonium strictum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1606
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SAROCLADIUM STRICTUM (UNII: 3F36V0451W) (SAROCLADIUM STRICTUM - UNII:3F36V0451W)	SAROCLADIUM STRICTUM	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1606-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

RHIZOPUS STOLONIFER 
rhizopus stolonifer solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2623
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q)	RHIZOPUS STOLONIFER	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2623-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-2623-4	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	BLA101833	09/15/1981

MUCOR CIRCINELLOIDES F. LUSITANICUS 
mucor circinelloides f. lusitanicus solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2671
Route of Administration	PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MUCOR CIRCINELLOIDES F. LUSITANICUS (UNII: 0J0X819B3C) (MUCOR CIRCINELLOIDES F. LUSITANICUS - UNII:0J0X819B3C)	MUCOR CIRCINELLOIDES F. LUSITANICUS	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2671-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

TRICHOTHECIUM ROSEUM 
trichothecium roseum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2654
Route of Administration	PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICHOTHECIUM ROSEUM (UNII: TGO054E31O) (TRICHOTHECIUM ROSEUM - UNII:TGO054E31O)	TRICHOTHECIUM ROSEUM	20000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2654-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-2654-4	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	BLA101833	09/15/1981

TRICHOTHECIUM ROSEUM 
trichothecium roseum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2656
Route of Administration	PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICHOTHECIUM ROSEUM (UNII: TGO054E31O) (TRICHOTHECIUM ROSEUM - UNII:TGO054E31O)	TRICHOTHECIUM ROSEUM	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2656-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

MYCOGONE PERNICIOSA 
mycogone perniciosa solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5642
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYPOMYCES PERNICIOSUS (UNII: 6K41G30A6U) (HYPOMYCES PERNICIOSUS - UNII:6K41G30A6U)	HYPOMYCES PERNICIOSUS	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5642-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5642-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-5642-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

MOLD MIX 2 
aureobasidium pullulans, curvularia spicifera, gibberella fujikuroi, mucor plumbeus and rhizopus stolonifer solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9609
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q)	RHIZOPUS STOLONIFER	2000 [PNU]  in 1 mL
COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD)	COCHLIOBOLUS SPICIFER	2000 [PNU]  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2)	GIBBERELLA FUJIKUROI	2000 [PNU]  in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK)	AUREOBASIDIUM PULLULANS VAR. PULLUTANS	2000 [PNU]  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E)	MUCOR PLUMBEUS	2000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9609-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9609-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

BIPOLARIS SOROKINIANA 
bipolaris sorokiniana solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1632
Route of Administration	INTRADERMAL, PERCUTANEOUS, 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 BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1632-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1632-4	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	BLA101833	09/15/1981

PENICILLIUM MIX 
penicillium camemberti, penicillium chrysogenum, penicillium digitatum, penicillium notatum and penicillium roqueforti solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9656
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PENICILLIUM DIGITATUM (UNII: 1SB49SV239) (PENICILLIUM DIGITATUM - UNII:1SB49SV239)	PENICILLIUM DIGITATUM	5000 [PNU]  in 1 mL
PENICILLIUM CAMEMBERTI (UNII: T069R9OPVG) (PENICILLIUM CAMEMBERTI - UNII:T069R9OPVG)	PENICILLIUM CAMEMBERTI	5000 [PNU]  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG)	PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM	5000 [PNU]  in 1 mL
PENICILLIUM ROQUEFORTI (UNII: 7ORP6R724L) (PENICILLIUM ROQUEFORTI - UNII:7ORP6R724L)	PENICILLIUM ROQUEFORTI	5000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9656-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

PENICILLIUM MIX 
penicillium camemberti, penicillium chrysogenum, penicillium digitatum, penicillium notatum and penicillium roqueforti solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9655
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PENICILLIUM DIGITATUM (UNII: 1SB49SV239) (PENICILLIUM DIGITATUM - UNII:1SB49SV239)	PENICILLIUM DIGITATUM	10000 [PNU]  in 1 mL
PENICILLIUM CAMEMBERTI (UNII: T069R9OPVG) (PENICILLIUM CAMEMBERTI - UNII:T069R9OPVG)	PENICILLIUM CAMEMBERTI	10000 [PNU]  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG)	PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM	10000 [PNU]  in 1 mL
PENICILLIUM ROQUEFORTI (UNII: 7ORP6R724L) (PENICILLIUM ROQUEFORTI - UNII:7ORP6R724L)	PENICILLIUM ROQUEFORTI	10000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9655-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9655-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

PENICILLIUM MIX 
penicillium camemberti, penicillium chrysogenum, penicillium digitatum, penicillium notatum and penicillium roqueforti solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9657
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PENICILLIUM DIGITATUM (UNII: 1SB49SV239) (PENICILLIUM DIGITATUM - UNII:1SB49SV239)	PENICILLIUM DIGITATUM	0.0125 g  in 1 mL
PENICILLIUM CAMEMBERTI (UNII: T069R9OPVG) (PENICILLIUM CAMEMBERTI - UNII:T069R9OPVG)	PENICILLIUM CAMEMBERTI	0.0125 g  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG)	PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM	0.0125 g  in 1 mL
PENICILLIUM ROQUEFORTI (UNII: 7ORP6R724L) (PENICILLIUM ROQUEFORTI - UNII:7ORP6R724L)	PENICILLIUM ROQUEFORTI	0.0125 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9657-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9657-4	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	BLA101833	09/15/1981

PENICILLIUM MIX 
penicillium camemberti, penicillium chrysogenum, penicillium digitatum, penicillium notatum and penicillium roqueforti solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9679
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PENICILLIUM DIGITATUM (UNII: 1SB49SV239) (PENICILLIUM DIGITATUM - UNII:1SB49SV239)	PENICILLIUM DIGITATUM	2500 [PNU]  in 1 mL
PENICILLIUM CAMEMBERTI (UNII: T069R9OPVG) (PENICILLIUM CAMEMBERTI - UNII:T069R9OPVG)	PENICILLIUM CAMEMBERTI	2500 [PNU]  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG)	PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM	2500 [PNU]  in 1 mL
PENICILLIUM ROQUEFORTI (UNII: 7ORP6R724L) (PENICILLIUM ROQUEFORTI - UNII:7ORP6R724L)	PENICILLIUM ROQUEFORTI	2500 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9679-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

ALTERNARIA ALTERNATA 
alternaria alternata solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1600
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	20000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
PHENOL (UNII: 339NCG44TV)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1600-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1600-4	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	BLA101833	09/15/1981

ALTERNARIA ALTERNATA 
alternaria alternata solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1601
Route of Administration	PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	40000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1601-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1601-4	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	BLA101833	09/15/1981

ASPERGILLUS FLAVUS 
aspergillus flavus solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1610
Route of Administration	PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13)	ASPERGILLUS FLAVUS	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1610-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1610-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

ASPERGILLUS FUMIGATUS 
aspergillus fumigatus solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1615
Route of Administration	INTRADERMAL, PERCUTANEOUS, 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 BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1615-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1615-4	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	BLA101833	09/15/1981

ASPERGILLUS NIGER 
aspergillus niger solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1625
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1625-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1625-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

CHAETOMIUM GLOBOSUM 
chaetomium globosum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1648
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A)	CHAETOMIUM GLOBOSUM	40000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1648-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1648-4	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	BLA101833	09/15/1981

CHAETOMIUM GLOBOSUM 
chaetomium globosum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1647
Route of Administration	INTRADERMAL, PERCUTANEOUS, 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 BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1647-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1647-4	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	BLA101833	09/15/1981

CHAETOMIUM GLOBOSUM 
chaetomium globosum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1650
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A)	CHAETOMIUM GLOBOSUM	20000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1650-4	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	BLA101833	09/15/1981

CHAETOMIUM GLOBOSUM 
chaetomium globosum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1651
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A)	CHAETOMIUM GLOBOSUM	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1651-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

MOLD MIX 3 
alternaria alternata, aspergillus niger, cladosporium sphaerospermum and penicillium notatum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9614
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R)	CLADOSPORIUM SPHAEROSPERMUM	0.00025 g  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	0.00025 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	0.00025 g  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG)	PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM	0.00025 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9614-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

MOLD MIX 3 
alternaria alternata, aspergillus niger, cladosporium sphaerospermum and penicillium notatum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9618
Route of Administration	SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R)	CLADOSPORIUM SPHAEROSPERMUM	10000 [PNU]  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	10000 [PNU]  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	10000 [PNU]  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG)	PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM	10000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9618-4	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	BLA101833	09/15/1981

ASPERGILLUS MIX 
aspergillus amstelodami, aspergillus flavus, aspergillus fumigatus, aspergillus nidulans and aspergillus niger solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9631
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	0.0002 g  in 1 mL
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48)	ASPERGILLUS FUMIGATUS	0.0002 g  in 1 mL
EUROTIUM AMSTELODAMI (UNII: D932NLL87Z) (EUROTIUM AMSTELODAMI - UNII:D932NLL87Z)	EUROTIUM AMSTELODAMI	0.0002 g  in 1 mL
ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13)	ASPERGILLUS FLAVUS	0.0002 g  in 1 mL
ASPERGILLUS NIDULANS (UNII: 242A53RB80) (ASPERGILLUS NIDULANS - UNII:242A53RB80)	ASPERGILLUS NIDULANS	0.0002 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9631-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

DEMATIACEAE MIX 
alternaria alternata, aureobasidium pullulans, bipolaris sorokiniana, cladosporium herbarum, curvularia spicifera and helminthosporium solani solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9634
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD)	COCHLIOBOLUS SPICIFER	0.0083 g  in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK)	AUREOBASIDIUM PULLULANS VAR. PULLUTANS	0.0083 g  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W)	COCHLIOBOLUS SATIVUS	0.0083 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	0.0083 g  in 1 mL
CLADOSPORIUM HERBARUM (UNII: O64JF11198) (CLADOSPORIUM HERBARUM - UNII:O64JF11198)	CLADOSPORIUM HERBARUM	0.0083 g  in 1 mL
HELMINTHOSPORIUM SOLANI (UNII: U6Z259H815) (HELMINTHOSPORIUM SOLANI - UNII:U6Z259H815)	HELMINTHOSPORIUM SOLANI	0.0083 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9634-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

NEW STOCK FUNGI MIX 
acremonium strictum, alternaria alternata, aspergillus niger, aureobasidium pullulans, bipolaris sorokiniana, botrytis cinerea, candida albicans, chaetomium globosum, cladosporium sphaerospermum, epicoccum nigrum, gibberella fujikuroi, mucor plumbeus, penicillium notatum, phoma betae, rhizopus stolonifer and trichophyton mentagrophytes solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9649
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2)	GIBBERELLA FUJIKUROI	0.00625 g  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E)	MUCOR PLUMBEUS	0.00625 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	0.00625 g  in 1 mL
ACREMONIUM STRICTUM (UNII: 3F36V0451W) (ACREMONIUM STRICTUM - UNII:3F36V0451W)	ACREMONIUM STRICTUM	0.00625 g  in 1 mL
BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7)	BOTRYTIS CINEREA	0.00625 g  in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R)	CLADOSPORIUM SPHAEROSPERMUM	0.00625 g  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG)	PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM	0.00625 g  in 1 mL
PLEOSPORA BETAE (UNII: V58BK047ES) (PLEOSPORA BETAE - UNII:V58BK047ES)	PLEOSPORA BETAE	0.00625 g  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W)	COCHLIOBOLUS SATIVUS	0.00625 g  in 1 mL
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC)	CANDIDA ALBICANS	0.00625 g  in 1 mL
CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A)	CHAETOMIUM GLOBOSUM	0.00625 g  in 1 mL
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q)	RHIZOPUS STOLONIFER	0.00625 g  in 1 mL
TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV)	TRICHOPHYTON MENTAGROPHYTES	0.00625 g  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	0.00625 g  in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK)	AUREOBASIDIUM PULLULANS VAR. PULLUTANS	0.00625 g  in 1 mL
EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7)	EPICOCCUM NIGRUM	0.00625 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9649-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9649-4	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	BLA101833	09/15/1981

NEW STOCK FUNGI MIX 
acremonium strictum, alternaria alternata, aspergillus niger, aureobasidium pullulans, bipolaris sorokiniana, botrytis cinerea, candida albicans, chaetomium globosum, cladosporium sphaerospermum, epicoccum nigrum, gibberella fujikuroi, mucor plumbeus, penicillium notatum, phoma betae, rhizopus stolonifer and trichophyton mentagrophytes solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9652
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q)	RHIZOPUS STOLONIFER	0.003125 g  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W)	COCHLIOBOLUS SATIVUS	0.003125 g  in 1 mL
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC)	CANDIDA ALBICANS	0.003125 g  in 1 mL
CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A)	CHAETOMIUM GLOBOSUM	0.003125 g  in 1 mL
TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV)	TRICHOPHYTON MENTAGROPHYTES	0.003125 g  in 1 mL
EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7)	EPICOCCUM NIGRUM	0.003125 g  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	0.003125 g  in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK)	AUREOBASIDIUM PULLULANS VAR. PULLUTANS	0.003125 g  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2)	GIBBERELLA FUJIKUROI	0.003125 g  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E)	MUCOR PLUMBEUS	0.003125 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	0.003125 g  in 1 mL
ACREMONIUM STRICTUM (UNII: 3F36V0451W) (ACREMONIUM STRICTUM - UNII:3F36V0451W)	ACREMONIUM STRICTUM	0.003125 g  in 1 mL
BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7)	BOTRYTIS CINEREA	0.003125 g  in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R)	CLADOSPORIUM SPHAEROSPERMUM	0.003125 g  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG)	PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM	0.003125 g  in 1 mL
PLEOSPORA BETAE (UNII: V58BK047ES) (PLEOSPORA BETAE - UNII:V58BK047ES)	PLEOSPORA BETAE	0.003125 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9652-4	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	BLA101833	09/15/1981

GRASS SMUT MIX 
ustilago cynodontis and sporisorium cruentum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9676
Route of Administration	PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
USTILAGO CYNODONTIS (UNII: 0V3J4YEX2W) (USTILAGO CYNODONTIS - UNII:0V3J4YEX2W)	USTILAGO CYNODONTIS	0.05 g  in 1 mL
SPORISORIUM CRUENTUM (UNII: GQM6LVU5V8) (SPORISORIUM CRUENTUM - UNII:GQM6LVU5V8)	SPORISORIUM CRUENTUM	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9676-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

DRECHSLERA SPICIFERA 
drechslera spicifera solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1664
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD)	COCHLIOBOLUS SPICIFER	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1664-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

DRECHSLERA SPICIFERA 
drechslera spicifera solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1662
Route of Administration	INTRADERMAL, SUBCUTANEOUS, PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD)	COCHLIOBOLUS SPICIFER	20000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1662-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

ALTERNARIA HORMODENDRUM MIX 
alternaria alternata and aspergillus fumigatus solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9626
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	0.025 g  in 1 mL
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48)	ASPERGILLUS FUMIGATUS	0.025 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9626-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9626-4	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	BLA101833	09/15/1981

HELMINTHOSPORIUM SOLANI 
helminthosporium solani solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1690
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HELMINTHOSPORIUM SOLANI (UNII: U6Z259H815) (HELMINTHOSPORIUM SOLANI - UNII:U6Z259H815)	HELMINTHOSPORIUM SOLANI	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1690-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

MUCOR PLUMBEUS 
mucor plumbeus solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1696
Route of Administration	SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E)	MUCOR PLUMBEUS	40000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1696-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

MUCOR PLUMBEUS 
mucor plumbeus solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5626
Route of Administration	SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E)	MUCOR PLUMBEUS	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5626-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5626-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

ASPERGILLUS NIDULANS 
aspergillus nidulans solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1622
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS NIDULANS (UNII: 242A53RB80) (ASPERGILLUS NIDULANS - UNII:242A53RB80)	ASPERGILLUS NIDULANS	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1622-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1622-4	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	BLA101833	09/15/1981

ASPERGILLUS NIDULANS 
aspergillus nidulans solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2660
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS NIDULANS (UNII: 242A53RB80) (ASPERGILLUS NIDULANS - UNII:242A53RB80)	ASPERGILLUS NIDULANS	20000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2660-4	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	BLA101833	09/15/1981

AUREOBASIDIUM PULLULANS 
aureobasidium pullulans solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1630
Route of Administration	INTRADERMAL, PERCUTANEOUS, 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	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1630-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

BIPOLARIS SOROKINIANA 
bipolaris sorokiniana solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1635
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W)	COCHLIOBOLUS SATIVUS	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1635-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1635-4	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	BLA101833	09/15/1981

BIPOLARIS SOROKINIANA 
bipolaris sorokiniana solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1636
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W)	COCHLIOBOLUS SATIVUS	0.01 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1636-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

BIPOLARIS SOROKINIANA 
bipolaris sorokiniana solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5608
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W)	COCHLIOBOLUS SATIVUS	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5608-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5608-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-5608-5	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

ASPERGILLUS FUMIGATUS 
aspergillus fumigatus solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1617
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48)	ASPERGILLUS FUMIGATUS	40000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1617-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1617-4	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	BLA101833	09/15/1981

ASPERGILLUS FUMIGATUS 
aspergillus fumigatus solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1618
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48)	ASPERGILLUS FUMIGATUS	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1618-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1618-4	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	BLA101833	09/15/1981

NEW STOCK FUNGI MIX 
acremonium strictum, alternaria alternata, aspergillus niger, aureobasidium pullulans, bipolaris sorokiniana, botrytis cinerea, candida albicans, chaetomium globosum, cladosporium sphaerospermum, epicoccum nigrum, gibberella fujikuroi, mucor plumbeus, penicillium notatum, phoma betae, rhizopus stolonifer and trichophyton mentagrophytes solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9650
Route of Administration	SUBCUTANEOUS, PERCUTANEOUS, INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2)	GIBBERELLA FUJIKUROI	0.0000625 g  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E)	MUCOR PLUMBEUS	0.0000625 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	0.0000625 g  in 1 mL
ACREMONIUM STRICTUM (UNII: 3F36V0451W) (ACREMONIUM STRICTUM - UNII:3F36V0451W)	ACREMONIUM STRICTUM	0.0000625 g  in 1 mL
BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7)	BOTRYTIS CINEREA	0.0000625 g  in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R)	CLADOSPORIUM SPHAEROSPERMUM	0.0000625 g  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG)	PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM	0.0000625 g  in 1 mL
PLEOSPORA BETAE (UNII: V58BK047ES) (PLEOSPORA BETAE - UNII:V58BK047ES)	PLEOSPORA BETAE	0.0000625 g  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W)	COCHLIOBOLUS SATIVUS	0.0000625 g  in 1 mL
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC)	CANDIDA ALBICANS	0.0000625 g  in 1 mL
CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A)	CHAETOMIUM GLOBOSUM	0.0000625 g  in 1 mL
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q)	RHIZOPUS STOLONIFER	0.0000625 g  in 1 mL
TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV)	TRICHOPHYTON MENTAGROPHYTES	0.0000625 g  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	0.0000625 g  in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK)	AUREOBASIDIUM PULLULANS VAR. PULLUTANS	0.0000625 g  in 1 mL
EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7)	EPICOCCUM NIGRUM	0.0000625 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9650-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

PENICILLIUM MIX 
penicillium camemberti, penicillium chrysogenum, penicillium digitatum, penicillium notatum and penicillium roqueforti solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9654
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PENICILLIUM DIGITATUM (UNII: 1SB49SV239) (PENICILLIUM DIGITATUM - UNII:1SB49SV239)	PENICILLIUM DIGITATUM	0.025 g  in 1 mL
PENICILLIUM CAMEMBERTI (UNII: T069R9OPVG) (PENICILLIUM CAMEMBERTI - UNII:T069R9OPVG)	PENICILLIUM CAMEMBERTI	0.025 g  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG)	PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM	0.025 g  in 1 mL
PENICILLIUM ROQUEFORTI (UNII: 7ORP6R724L) (PENICILLIUM ROQUEFORTI - UNII:7ORP6R724L)	PENICILLIUM ROQUEFORTI	0.025 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9654-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9654-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

GRASS SMUT MIX 
ustilago cynodontis and sporisorium cruentum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9671
Route of Administration	PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL

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
USTILAGO CYNODONTIS (UNII: 0V3J4YEX2W) (USTILAGO CYNODONTIS - UNII:0V3J4YEX2W)	USTILAGO CYNODONTIS	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9671-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9671-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-9671-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

GRAIN SMUT MIX 
ustilago maydis, ustilago tritici, ustilago nuda and ustilago avenae solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9675
Route of Administration	PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
USTILAGO NUDA (UNII: 9Y53ZS6I82) (USTILAGO NUDA - UNII:9Y53ZS6I82)	USTILAGO NUDA	0.0125 g  in 1 mL
USTILAGO AVENAE (UNII: YIH315U1TU) (USTILAGO AVENAE - UNII:YIH315U1TU)	USTILAGO AVENAE	0.0125 g  in 1 mL
USTILAGO MAYDIS (UNII: 4K7Z7K7SWG) (USTILAGO MAYDIS - UNII:4K7Z7K7SWG)	USTILAGO MAYDIS	0.0125 g  in 1 mL
USTILAGO TRITICI (UNII: BV82OL2IZ8) (USTILAGO TRITICI - UNII:BV82OL2IZ8)	USTILAGO TRITICI	0.0125 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9675-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

CANDIDA ALBICANS 
candida albicans solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1641
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC)	CANDIDA ALBICANS	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1641-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1641-4	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	BLA101833	09/15/1981

CORN SMUT 
ustilago maydis solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2664
Route of Administration	PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
USTILAGO MAYDIS (UNII: 4K7Z7K7SWG) (USTILAGO MAYDIS - UNII:4K7Z7K7SWG)	USTILAGO MAYDIS	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2664-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

CANDIDA ALBICANS 
candida albicans solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1643
Route of Administration	INTRADERMAL, PERCUTANEOUS, 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 BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1643-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

EPIDERMOPHYTON FLOCCOSUM 
epidermophyton floccosum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1667
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EPIDERMOPHYTON FLOCCOSUM (UNII: 6JR6JTN25S) (EPIDERMOPHYTON FLOCCOSUM - UNII:6JR6JTN25S)	EPIDERMOPHYTON FLOCCOSUM	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1667-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1667-4	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	BLA101833	09/15/1981

EPIDERMOPHYTON FLOCCOSUM 
epidermophyton floccosum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1669
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EPIDERMOPHYTON FLOCCOSUM (UNII: 6JR6JTN25S) (EPIDERMOPHYTON FLOCCOSUM - UNII:6JR6JTN25S)	EPIDERMOPHYTON FLOCCOSUM	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1669-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

CLADOSPORIUM SPHAEROSPERMUM 
cladosporium sphaerospermum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1659
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R)	CLADOSPORIUM SPHAEROSPERMUM	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1659-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

DRECHSLERA SPICIFERA 
drechslera spicifera solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1661
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD)	COCHLIOBOLUS SPICIFER	40000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1661-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1661-4	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	BLA101833	09/15/1981

PAECILOMYCES VARIOTII 
paecilomyces variotii solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2606
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PAECILOMYCES VARIOTII (UNII: KO7V58BY40) (PAECILOMYCES VARIOTII - UNII:KO7V58BY40)	PAECILOMYCES VARIOTII	20000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2606-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-2606-4	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	BLA101833	09/15/1981

TRICHODERMA HARZIANUM 
trichoderma harzianum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5638
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICHODERMA HARZIANUM (UNII: CA33Q4013Q) (TRICHODERMA HARZIANUM - UNII:CA33Q4013Q)	TRICHODERMA HARZIANUM	0.025 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5638-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5638-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-5638-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

TRICHOPHYTON MENTAGROPHYTES 
trichophyton mentagrophytes solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2645
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV)	TRICHOPHYTON MENTAGROPHYTES	20000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2645-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-2645-4	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	BLA101833	09/15/1981

FUSARIUM MONILIFORME 
fusarium moniliforme solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1673
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2)	GIBBERELLA FUJIKUROI	40000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1673-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

FUSARIUM SOLANI 
fusarium solani solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1678
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HAEMATONECTRIA HAEMATOCOCCA (UNII: 7TLR512M4A) (HAEMATONECTRIA HAEMATOCOCCA - UNII:7TLR512M4A)	HAEMATONECTRIA HAEMATOCOCCA	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1678-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

MOLD MIX 1 
alternaria alternata, aspergillus niger, bipolaris sorokiniana, cladosporium sphaerospermum and penicillium notatum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9601
Route of Administration	INTRADERMAL, PERCUTANEOUS, 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	4000 [PNU]  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	4000 [PNU]  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W)	COCHLIOBOLUS SATIVUS	4000 [PNU]  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	4000 [PNU]  in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R)	CLADOSPORIUM SPHAEROSPERMUM	4000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9601-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9601-4	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	BLA101833	09/15/1981

FUSARIUM MONILIFORME 
fusarium moniliforme solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1674
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2)	GIBBERELLA FUJIKUROI	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1674-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

FUSARIUM SOLANI 
fusarium solani solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1677
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HAEMATONECTRIA HAEMATOCOCCA (UNII: 7TLR512M4A) (HAEMATONECTRIA HAEMATOCOCCA - UNII:7TLR512M4A)	HAEMATONECTRIA HAEMATOCOCCA	20000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1677-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

GEOTRICHUM CANDIDUM 
geotrichum candidum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1680
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GEOTRICHUM CANDIDUM (UNII: 5964J742O8) (GEOTRICHUM CANDIDUM - UNII:5964J742O8)	GEOTRICHUM CANDIDUM	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1680-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

GLIOCLADIUM VIRIDE 
gliocladium viride solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5621
Route of Administration	PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLIOCLADIUM VIRIDE (UNII: 8Z8C642TPL) (GLIOCLADIUM VIRIDE - UNII:8Z8C642TPL)	GLIOCLADIUM VIRIDE	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5621-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5621-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-5621-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

MUCOR PLUMBEUS 
mucor plumbeus solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1698
Route of Administration	SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E)	MUCOR PLUMBEUS	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1698-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

NEUROSPORA INTERMEDIA 
neurospora intermedia solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2601
Route of Administration	PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI)	NEUROSPORA INTERMEDIA	20000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2601-4	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	BLA101833	09/15/1981

PAECILOMYCES VARIOTII 
paecilomyces variotii solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2609
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PAECILOMYCES VARIOTII (UNII: KO7V58BY40) (PAECILOMYCES VARIOTII - UNII:KO7V58BY40)	PAECILOMYCES VARIOTII	40000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2609-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-2609-4	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	BLA101833	09/15/1981

PAECILOMYCES VARIOTII 
paecilomyces variotii solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5629
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PAECILOMYCES VARIOTII (UNII: KO7V58BY40) (PAECILOMYCES VARIOTII - UNII:KO7V58BY40)	PAECILOMYCES VARIOTII	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5629-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5629-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-5629-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

PENICILLIUM CHRYSOGENUM (NOTATUM) 
penicillium chrysogenum (notatum) solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2614
Route of Administration	INTRADERMAL, PERCUTANEOUS, 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 BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2614-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-2614-4	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	BLA101833	09/15/1981

PHOMA BETAE 
phoma betae solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2674
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PLEOSPORA BETAE (UNII: V58BK047ES) (PLEOSPORA BETAE - UNII:V58BK047ES)	PLEOSPORA BETAE	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2674-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

MUCOR CIRCINELLOIDES F. CIRCINELLOIDES 
mucor circinelloides f. circinelloides solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5624
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MUCOR CIRCINELLOIDES F. CIRCINELLOIDES (UNII: 48Z8OUT98B) (MUCOR CIRCINELLOIDES F. CIRCINELLOIDES - UNII:48Z8OUT98B)	MUCOR CIRCINELLOIDES F. CIRCINELLOIDES	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5624-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5624-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

PAECILOMYCES VARIOTII 
paecilomyces variotii solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2607
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PAECILOMYCES VARIOTII (UNII: KO7V58BY40) (PAECILOMYCES VARIOTII - UNII:KO7V58BY40)	PAECILOMYCES VARIOTII	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2607-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

ASPERGILLUS FUMIGATUS 
aspergillus fumigatus solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1621
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48)	ASPERGILLUS FUMIGATUS	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1621-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

RHIZOPUS STOLONIFER 
rhizopus stolonifer solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2624
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q)	RHIZOPUS STOLONIFER	40000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2624-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-2624-4	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	BLA101833	09/15/1981

RHIZOPUS STOLONIFER 
rhizopus stolonifer solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2625
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q)	RHIZOPUS STOLONIFER	20000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2625-4	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	BLA101833	09/15/1981

SACCHAROMYCES CEREVISIAE 
saccharomyces cerevisiae solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2634
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) (SACCHAROMYCES CEREVISIAE - UNII:978D8U419H)	SACCHAROMYCES CEREVISIAE	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2634-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-2634-4	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	BLA101833	09/15/1981

SACCHAROMYCES CEREVISIAE 
saccharomyces cerevisiae solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2677
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) (SACCHAROMYCES CEREVISIAE - UNII:978D8U419H)	SACCHAROMYCES CEREVISIAE	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2677-4	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	BLA101833	09/15/1981

TRICHOPHYTON MENTAGROPHYTES 
trichophyton mentagrophytes solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2646
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV)	TRICHOPHYTON MENTAGROPHYTES	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2646-4	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	BLA101833	09/15/1981

TRICHOPHYTON RUBRUM 
trichophyton rubrum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5640
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICHOPHYTON RUBRUM (UNII: 2ZAU32517N) (TRICHOPHYTON RUBRUM - UNII:2ZAU32517N)	TRICHOPHYTON RUBRUM	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5640-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5640-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

MOLD MIX 1 
alternaria alternata, aspergillus niger, bipolaris sorokiniana, cladosporium sphaerospermum and penicillium notatum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9602
Route of Administration	INTRADERMAL, PERCUTANEOUS, 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	8000 [PNU]  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	8000 [PNU]  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W)	COCHLIOBOLUS SATIVUS	8000 [PNU]  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	8000 [PNU]  in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R)	CLADOSPORIUM SPHAEROSPERMUM	8000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9602-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9602-4	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	BLA101833	09/15/1981

MOLD MIX 1 
alternaria alternata, aspergillus niger, bipolaris sorokiniana, cladosporium sphaerospermum and penicillium notatum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9604
Route of Administration	INTRADERMAL, PERCUTANEOUS, 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	0.0002 g  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	0.0002 g  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W)	COCHLIOBOLUS SATIVUS	0.0002 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	0.0002 g  in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R)	CLADOSPORIUM SPHAEROSPERMUM	0.0002 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9604-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

MOLD MIX 1 
alternaria alternata, aspergillus niger, bipolaris sorokiniana, cladosporium sphaerospermum and penicillium notatum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9606
Route of Administration	INTRADERMAL, PERCUTANEOUS, 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	0.01 g  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	0.01 g  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W)	COCHLIOBOLUS SATIVUS	0.01 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	0.01 g  in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R)	CLADOSPORIUM SPHAEROSPERMUM	0.01 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9606-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9606-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-9606-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

MOLD MIX 2 
aureobasidium pullulans, curvularia spicifera, gibberella fujikuroi, mucor plumbeus and rhizopus stolonifer solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9608
Route of Administration	PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q)	RHIZOPUS STOLONIFER	4000 [PNU]  in 1 mL
COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD)	COCHLIOBOLUS SPICIFER	4000 [PNU]  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2)	GIBBERELLA FUJIKUROI	4000 [PNU]  in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK)	AUREOBASIDIUM PULLULANS VAR. PULLUTANS	4000 [PNU]  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E)	MUCOR PLUMBEUS	4000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9608-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9608-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

ACREMONIUM STRICTUM 
acremonium strictum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2679
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SAROCLADIUM STRICTUM (UNII: 3F36V0451W) (SAROCLADIUM STRICTUM - UNII:3F36V0451W)	SAROCLADIUM STRICTUM	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2679-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

BOTRYTIS CINEREA 
botrytis cinerea solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5609
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7)	BOTRYTIS CINEREA	0.025 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5609-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5609-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

CANDIDA ALBICANS 
candida albicans solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1646
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC)	CANDIDA ALBICANS	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1646-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

RHIZOPUS STOLONIFER 
rhizopus stolonifer solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2627
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q)	RHIZOPUS STOLONIFER	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2627-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

RHIZOPUS STOLONIFER 
rhizopus stolonifer solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5634
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q)	RHIZOPUS STOLONIFER	0.025 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5634-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5634-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

RHODOTORULA MUCILAGINOSA 
rhodotorula mucilaginosa solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2628
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHODOTORULA MUCILAGINOSA (UNII: 62TY3X4N9Z) (RHODOTORULA MUCILAGINOSA - UNII:62TY3X4N9Z)	RHODOTORULA MUCILAGINOSA	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2628-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

CANDIDA ALBICANS 
candida albicans solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5610
Route of Administration	INTRADERMAL, PERCUTANEOUS, 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
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5610-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5610-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

CLADOSPORIUM HERBARUM 
cladosporium herbarum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5613
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLADOSPORIUM HERBARUM (UNII: O64JF11198) (CLADOSPORIUM HERBARUM - UNII:O64JF11198)	CLADOSPORIUM HERBARUM	0.025 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5613-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2	NDC: 22840-5613-4	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	BLA101833	09/15/1981

MOLD MIX 1 
alternaria alternata, aspergillus niger, bipolaris sorokiniana, cladosporium sphaerospermum and penicillium notatum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9600
Route of Administration	INTRADERMAL, PERCUTANEOUS, 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	0.02 g  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	0.02 g  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W)	COCHLIOBOLUS SATIVUS	0.02 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	0.02 g  in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R)	CLADOSPORIUM SPHAEROSPERMUM	0.02 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9600-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9600-4	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	BLA101833	09/15/1981

GLIOCLADIUM VIRIDE 
gliocladium viride solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1683
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLIOCLADIUM VIRIDE (UNII: 8Z8C642TPL) (GLIOCLADIUM VIRIDE - UNII:8Z8C642TPL)	GLIOCLADIUM VIRIDE	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1683-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

PENICILLIUM MIX 
penicillium camemberti, penicillium chrysogenum, penicillium digitatum, penicillium notatum and penicillium roqueforti solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9660
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PENICILLIUM DIGITATUM (UNII: 1SB49SV239) (PENICILLIUM DIGITATUM - UNII:1SB49SV239)	PENICILLIUM DIGITATUM	0.0125 g  in 1 mL
PENICILLIUM CAMEMBERTI (UNII: T069R9OPVG) (PENICILLIUM CAMEMBERTI - UNII:T069R9OPVG)	PENICILLIUM CAMEMBERTI	0.0125 g  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG)	PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM	0.0125 g  in 1 mL
PENICILLIUM ROQUEFORTI (UNII: 7ORP6R724L) (PENICILLIUM ROQUEFORTI - UNII:7ORP6R724L)	PENICILLIUM ROQUEFORTI	0.0125 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9660-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9660-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-9660-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

PENICILLIUM MIX 
penicillium camemberti, penicillium chrysogenum, penicillium digitatum, penicillium notatum and penicillium roqueforti solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9659
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PENICILLIUM CAMEMBERTI (UNII: T069R9OPVG) (PENICILLIUM CAMEMBERTI - UNII:T069R9OPVG)	PENICILLIUM CAMEMBERTI	0.00025 g  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG)	PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM	0.00025 g  in 1 mL
PENICILLIUM ROQUEFORTI (UNII: 7ORP6R724L) (PENICILLIUM ROQUEFORTI - UNII:7ORP6R724L)	PENICILLIUM ROQUEFORTI	0.00025 g  in 1 mL
PENICILLIUM DIGITATUM (UNII: 1SB49SV239) (PENICILLIUM DIGITATUM - UNII:1SB49SV239)	PENICILLIUM DIGITATUM	0.00025 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9659-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

PHYCOMYCETES MIX 
mucor circinelloides f. lusitanicus and rhizopus stolonifer solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9661
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MUCOR CIRCINELLOIDES F. LUSITANICUS (UNII: 0J0X819B3C) (MUCOR CIRCINELLOIDES F. LUSITANICUS - UNII:0J0X819B3C)	MUCOR CIRCINELLOIDES F. LUSITANICUS	0.025 g  in 1 mL
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q)	RHIZOPUS STOLONIFER	0.025 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9661-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

PHYCOMYCETES MIX 
mucor circinelloides f. lusitanicus and rhizopus stolonifer solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9662
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MUCOR CIRCINELLOIDES F. LUSITANICUS (UNII: 0J0X819B3C) (MUCOR CIRCINELLOIDES F. LUSITANICUS - UNII:0J0X819B3C)	MUCOR CIRCINELLOIDES F. LUSITANICUS	0.0005 g  in 1 mL
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q)	RHIZOPUS STOLONIFER	0.0005 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9662-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

PHYCOMYCETES MIX 
mucor circinelloides f. lusitanicus and rhizopus stolonifer solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9664
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MUCOR CIRCINELLOIDES F. LUSITANICUS (UNII: 0J0X819B3C) (MUCOR CIRCINELLOIDES F. LUSITANICUS - UNII:0J0X819B3C)	MUCOR CIRCINELLOIDES F. LUSITANICUS	0.0125 g  in 1 mL
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q)	RHIZOPUS STOLONIFER	0.0125 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9664-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9664-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-9664-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

RHIZOPUS MIX 
rhizopus stolonifer and rhizopus oryzae solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9665
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q)	RHIZOPUS STOLONIFER	0.025 g  in 1 mL
RHIZOPUS ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS - UNII:8476849N1Y)	RHIZOPUS ARRHIZUS	0.025 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9665-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9665-4	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	BLA101833	09/15/1981

RHIZOPUS MIX 
rhizopus stolonifer and rhizopus oryzae solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9666
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q)	RHIZOPUS STOLONIFER	20000 [PNU]  in 1 mL
RHIZOPUS ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS - UNII:8476849N1Y)	RHIZOPUS ARRHIZUS	20000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9666-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

RHIZOPUS MIX 
rhizopus stolonifer and rhizopus oryzae solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9668
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q)	RHIZOPUS STOLONIFER	0.0005 g  in 1 mL
RHIZOPUS ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS - UNII:8476849N1Y)	RHIZOPUS ARRHIZUS	0.0005 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9668-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

ASPERGILLUS FLAVUS 
aspergillus flavus solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1612
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13)	ASPERGILLUS FLAVUS	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1612-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

BIPOLARIS SOROKINIANA 
bipolaris sorokiniana solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2661
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W)	COCHLIOBOLUS SATIVUS	10000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2661-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

PENICILLIUM DIGITATUM 
penicillium digitatum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2610
Route of Administration	INTRADERMAL, SUBCUTANEOUS, PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PENICILLIUM DIGITATUM (UNII: 1SB49SV239) (PENICILLIUM DIGITATUM - UNII:1SB49SV239)	PENICILLIUM DIGITATUM	0.025 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2610-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-2610-4	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	BLA101833	09/15/1981

MUCOR MIX 
mucor circinelloides f. lusitanicus and mucor plumbeus solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9672
Route of Administration	PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MUCOR CIRCINELLOIDES F. LUSITANICUS (UNII: 0J0X819B3C) (MUCOR CIRCINELLOIDES F. LUSITANICUS - UNII:0J0X819B3C)	MUCOR CIRCINELLOIDES F. LUSITANICUS	0.05 g  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E)	MUCOR PLUMBEUS	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9672-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

MOLD MIX 2 
aureobasidium pullulans, curvularia spicifera, gibberella fujikuroi, mucor plumbeus and rhizopus stolonifer solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9607
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q)	RHIZOPUS STOLONIFER	0.01 g  in 1 mL
COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD)	COCHLIOBOLUS SPICIFER	0.01 g  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2)	GIBBERELLA FUJIKUROI	0.01 g  in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK)	AUREOBASIDIUM PULLULANS VAR. PULLUTANS	0.01 g  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E)	MUCOR PLUMBEUS	0.01 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9607-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9607-4	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	BLA101833	09/15/1981

ASPERGILLUS MIX 
aspergillus amstelodami, aspergillus flavus, aspergillus fumigatus, aspergillus nidulans and aspergillus niger solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9628
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	8000 [PNU]  in 1 mL
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48)	ASPERGILLUS FUMIGATUS	8000 [PNU]  in 1 mL
EUROTIUM AMSTELODAMI (UNII: D932NLL87Z) (EUROTIUM AMSTELODAMI - UNII:D932NLL87Z)	EUROTIUM AMSTELODAMI	8000 [PNU]  in 1 mL
ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13)	ASPERGILLUS FLAVUS	8000 [PNU]  in 1 mL
ASPERGILLUS NIDULANS (UNII: 242A53RB80) (ASPERGILLUS NIDULANS - UNII:242A53RB80)	ASPERGILLUS NIDULANS	8000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9628-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9628-4	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	BLA101833	09/15/1981

ASPERGILLUS MIX 
aspergillus amstelodami, aspergillus flavus, aspergillus fumigatus, aspergillus nidulans and aspergillus niger solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9633
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	0.01 g  in 1 mL
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48)	ASPERGILLUS FUMIGATUS	0.01 g  in 1 mL
EUROTIUM AMSTELODAMI (UNII: D932NLL87Z) (EUROTIUM AMSTELODAMI - UNII:D932NLL87Z)	EUROTIUM AMSTELODAMI	0.01 g  in 1 mL
ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13)	ASPERGILLUS FLAVUS	0.01 g  in 1 mL
ASPERGILLUS NIDULANS (UNII: 242A53RB80) (ASPERGILLUS NIDULANS - UNII:242A53RB80)	ASPERGILLUS NIDULANS	0.01 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9633-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9633-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-9633-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

MONILIA MIX 
candida albicans and neurospora intermedia solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9644
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC)	CANDIDA ALBICANS	0.0005 g  in 1 mL
NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI)	NEUROSPORA INTERMEDIA	0.0005 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9644-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

ASPERGILLUS FUMIGATUS 
aspergillus fumigatus solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1616
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48)	ASPERGILLUS FUMIGATUS	20000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1616-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

ASPERGILLUS FLAVUS 
aspergillus flavus solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1614
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13)	ASPERGILLUS FLAVUS	40000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1614-4	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	BLA101833	09/15/1981

ASPERGILLUS FUMIGATUS 
aspergillus fumigatus solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5604
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48)	ASPERGILLUS FUMIGATUS	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5604-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5604-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-5604-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

AUREOBASIDIUM PULLULANS 
aureobasidium pullulans solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5607
Route of Administration	INTRADERMAL, PERCUTANEOUS, 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	0.025 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5607-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2	NDC: 22840-5607-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-5607-4	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	BLA101833	09/15/1981

MOLD MIX 3 
alternaria alternata, aspergillus niger, cladosporium sphaerospermum and penicillium notatum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9620
Route of Administration	INTRADERMAL, SUBCUTANEOUS, PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R)	CLADOSPORIUM SPHAEROSPERMUM	0.0125 g  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	0.0125 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	0.0125 g  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG)	PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM	0.0125 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9620-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9620-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-9620-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

MOLD MIX 2 
aureobasidium pullulans, curvularia spicifera, gibberella fujikuroi, mucor plumbeus and rhizopus stolonifer solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-9613
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q)	RHIZOPUS STOLONIFER	0.005 g  in 1 mL
COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD)	COCHLIOBOLUS SPICIFER	0.005 g  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2)	GIBBERELLA FUJIKUROI	0.005 g  in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK)	AUREOBASIDIUM PULLULANS VAR. PULLUTANS	0.005 g  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E)	MUCOR PLUMBEUS	0.005 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-9613-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-9613-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-9613-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

DRECHSLERA SPICIFERA 
drechslera spicifera solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1660
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD)	COCHLIOBOLUS SPICIFER	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1660-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1660-4	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	BLA101833	09/15/1981

EPIDERMOPHYTON FLOCCOSUM 
epidermophyton floccosum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2666
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EPIDERMOPHYTON FLOCCOSUM (UNII: 6JR6JTN25S) (EPIDERMOPHYTON FLOCCOSUM - UNII:6JR6JTN25S)	EPIDERMOPHYTON FLOCCOSUM	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2666-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

MUCOR CIRCINELLOIDES F. CIRCINELLOIDES 
mucor circinelloides f. circinelloides solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1692
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MUCOR CIRCINELLOIDES F. CIRCINELLOIDES (UNII: 48Z8OUT98B) (MUCOR CIRCINELLOIDES F. CIRCINELLOIDES - UNII:48Z8OUT98B)	MUCOR CIRCINELLOIDES F. CIRCINELLOIDES	20000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1692-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

MUCOR CIRCINELLOIDES F. CIRCINELLOIDES 
mucor circinelloides f. circinelloides solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2670
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MUCOR CIRCINELLOIDES F. CIRCINELLOIDES (UNII: 48Z8OUT98B) (MUCOR CIRCINELLOIDES F. CIRCINELLOIDES - UNII:48Z8OUT98B)	MUCOR CIRCINELLOIDES F. CIRCINELLOIDES	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2670-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

NEUROSPORA INTERMEDIA 
neurospora intermedia solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1699
Route of Administration	PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI)	NEUROSPORA INTERMEDIA	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1699-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1699-4	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	BLA101833	09/15/1981

NEUROSPORA INTERMEDIA 
neurospora intermedia solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2602
Route of Administration	SUBCUTANEOUS, PERCUTANEOUS, INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI)	NEUROSPORA INTERMEDIA	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2602-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

PAECILOMYCES VARIOTII 
paecilomyces variotii solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2673
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PAECILOMYCES VARIOTII (UNII: KO7V58BY40) (PAECILOMYCES VARIOTII - UNII:KO7V58BY40)	PAECILOMYCES VARIOTII	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2673-4	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	BLA101833	09/15/1981

PENICILLIUM CHRYSOGENUM (NOTATUM) 
penicillium chrysogenum (notatum) solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2616
Route of Administration	INTRADERMAL, PERCUTANEOUS, 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	20000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2616-4	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	BLA101833	09/15/1981

PHOMA BETAE 
phoma betae solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2618
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PLEOSPORA BETAE (UNII: V58BK047ES) (PLEOSPORA BETAE - UNII:V58BK047ES)	PLEOSPORA BETAE	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2618-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

FUSARIUM MONILIFORME 
fusarium moniliforme solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1672
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2)	GIBBERELLA FUJIKUROI	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1672-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

GEOTRICHUM CANDIDUM 
geotrichum candidum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5620
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GEOTRICHUM CANDIDUM (UNII: 5964J742O8) (GEOTRICHUM CANDIDUM - UNII:5964J742O8)	GEOTRICHUM CANDIDUM	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5620-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5620-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-5620-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

PENICILLIUM CHRYSOGENUM (NOTATUM) 
penicillium chrysogenum (notatum) solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2612
Route of Administration	INTRADERMAL, PERCUTANEOUS, 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	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2612-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

RHIZOPUS ORYZAE 
rhizopus oryzae solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2621
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHIZOPUS ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS - UNII:8476849N1Y)	RHIZOPUS ARRHIZUS	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2621-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

RHODOTORULA MUCILAGINOSA 
rhodotorula mucilaginosa solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2630
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHODOTORULA MUCILAGINOSA (UNII: 62TY3X4N9Z) (RHODOTORULA MUCILAGINOSA - UNII:62TY3X4N9Z)	RHODOTORULA MUCILAGINOSA	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2630-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-2630-4	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	BLA101833	09/15/1981

SACCHAROMYCES CEREVISIAE 
saccharomyces cerevisiae solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2633
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) (SACCHAROMYCES CEREVISIAE - UNII:978D8U419H)	SACCHAROMYCES CEREVISIAE	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2633-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

ALTERNARIA ALTERNATA 
alternaria alternata solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1602
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1602-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1602-4	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	BLA101833	09/15/1981

FUSARIUM MONILIFORME 
fusarium moniliforme solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5618
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2)	GIBBERELLA FUJIKUROI	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5618-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5618-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-5618-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

GEOTRICHUM CANDIDUM 
geotrichum candidum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2667
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GEOTRICHUM CANDIDUM (UNII: 5964J742O8) (GEOTRICHUM CANDIDUM - UNII:5964J742O8)	GEOTRICHUM CANDIDUM	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2667-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

GLIOCLADIUM VIRIDE 
gliocladium viride solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1685
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLIOCLADIUM VIRIDE (UNII: 8Z8C642TPL) (GLIOCLADIUM VIRIDE - UNII:8Z8C642TPL)	GLIOCLADIUM VIRIDE	20000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1685-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1685-4	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	BLA101833	09/15/1981

GLIOCLADIUM VIRIDE 
gliocladium viride solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1686
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLIOCLADIUM VIRIDE (UNII: 8Z8C642TPL) (GLIOCLADIUM VIRIDE - UNII:8Z8C642TPL)	GLIOCLADIUM VIRIDE	40000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1686-4	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	BLA101833	09/15/1981

HELMINTHOSPORIUM SOLANI 
helminthosporium solani solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1689
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HELMINTHOSPORIUM SOLANI (UNII: U6Z259H815) (HELMINTHOSPORIUM SOLANI - UNII:U6Z259H815)	HELMINTHOSPORIUM SOLANI	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1689-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1689-4	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	BLA101833	09/15/1981

MUCOR PLUMBEUS 
mucor plumbeus solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1695
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E)	MUCOR PLUMBEUS	20000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1695-4	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	BLA101833	09/15/1981

MUCOR PLUMBEUS 
mucor plumbeus solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2672
Route of Administration	SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E)	MUCOR PLUMBEUS	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2672-4	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	BLA101833	09/15/1981

PAECILOMYCES VARIOTII 
paecilomyces variotii solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2608
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PAECILOMYCES VARIOTII (UNII: KO7V58BY40) (PAECILOMYCES VARIOTII - UNII:KO7V58BY40)	PAECILOMYCES VARIOTII	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2608-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

RHIZOPUS ORYZAE 
rhizopus oryzae solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2620
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHIZOPUS ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS - UNII:8476849N1Y)	RHIZOPUS ARRHIZUS	20000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2620-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

HELMINTHOSPORIUM SOLANI 
helminthosporium solani solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1687
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HELMINTHOSPORIUM SOLANI (UNII: U6Z259H815) (HELMINTHOSPORIUM SOLANI - UNII:U6Z259H815)	HELMINTHOSPORIUM SOLANI	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1687-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

RHODOTORULA MUCILAGINOSA 
rhodotorula mucilaginosa solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2631
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHODOTORULA MUCILAGINOSA (UNII: 62TY3X4N9Z) (RHODOTORULA MUCILAGINOSA - UNII:62TY3X4N9Z)	RHODOTORULA MUCILAGINOSA	40000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2631-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

RHODOTORULA MUCILAGINOSA 
rhodotorula mucilaginosa solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2675
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHODOTORULA MUCILAGINOSA (UNII: 62TY3X4N9Z) (RHODOTORULA MUCILAGINOSA - UNII:62TY3X4N9Z)	RHODOTORULA MUCILAGINOSA	20000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2675-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

RHODOTORULA MUCILAGINOSA 
rhodotorula mucilaginosa solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5635
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RHODOTORULA MUCILAGINOSA (UNII: 62TY3X4N9Z) (RHODOTORULA MUCILAGINOSA - UNII:62TY3X4N9Z)	RHODOTORULA MUCILAGINOSA	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5635-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5635-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-5635-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

TRICHODERMA HARZIANUM 
trichoderma harzianum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2641
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICHODERMA HARZIANUM (UNII: CA33Q4013Q) (TRICHODERMA HARZIANUM - UNII:CA33Q4013Q)	TRICHODERMA HARZIANUM	40000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2641-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-2641-4	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	BLA101833	09/15/1981

TRICHODERMA HARZIANUM 
trichoderma harzianum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2680
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICHODERMA HARZIANUM (UNII: CA33Q4013Q) (TRICHODERMA HARZIANUM - UNII:CA33Q4013Q)	TRICHODERMA HARZIANUM	20000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2680-4	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	BLA101833	09/15/1981

TRICHOPHYTON MENTAGROPHYTES 
trichophyton mentagrophytes solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2644
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV)	TRICHOPHYTON MENTAGROPHYTES	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2644-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

TRICHOPHYTON MENTAGROPHYTES 
trichophyton mentagrophytes solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2648
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV)	TRICHOPHYTON MENTAGROPHYTES	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2648-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

TRICHOPHYTON MENTAGROPHYTES 
trichophyton mentagrophytes solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5639
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV)	TRICHOPHYTON MENTAGROPHYTES	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5639-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5639-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

TRICHOPHYTON RUBRUM 
trichophyton rubrum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2650
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICHOPHYTON RUBRUM (UNII: 2ZAU32517N) (TRICHOPHYTON RUBRUM - UNII:2ZAU32517N)	TRICHOPHYTON RUBRUM	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2650-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

TRICHOPHYTON RUBRUM 
trichophyton rubrum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2681
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICHOPHYTON RUBRUM (UNII: 2ZAU32517N) (TRICHOPHYTON RUBRUM - UNII:2ZAU32517N)	TRICHOPHYTON RUBRUM	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2681-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

TRICHOTHECIUM ROSEUM 
trichothecium roseum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2652
Route of Administration	PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICHOTHECIUM ROSEUM (UNII: TGO054E31O) (TRICHOTHECIUM ROSEUM - UNII:TGO054E31O)	TRICHOTHECIUM ROSEUM	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2652-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-2652-4	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	BLA101833	09/15/1981

TRICHOTHECIUM ROSEUM 
trichothecium roseum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2653
Route of Administration	PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICHOTHECIUM ROSEUM (UNII: TGO054E31O) (TRICHOTHECIUM ROSEUM - UNII:TGO054E31O)	TRICHOTHECIUM ROSEUM	40000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2653-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-2653-4	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	BLA101833	09/15/1981

TRICHOTHECIUM ROSEUM 
trichothecium roseum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2655
Route of Administration	PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICHOTHECIUM ROSEUM (UNII: TGO054E31O) (TRICHOTHECIUM ROSEUM - UNII:TGO054E31O)	TRICHOTHECIUM ROSEUM	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2655-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

TRICHOTHECIUM ROSEUM 
trichothecium roseum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5641
Route of Administration	SUBCUTANEOUS, PERCUTANEOUS, INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICHOTHECIUM ROSEUM (UNII: TGO054E31O) (TRICHOTHECIUM ROSEUM - UNII:TGO054E31O)	TRICHOTHECIUM ROSEUM	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5641-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5641-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-5641-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

ALTERNARIA ALTERNATA 
alternaria alternata solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5600
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5600-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2	NDC: 22840-5600-4	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	BLA101833	09/15/1981

SACCHAROMYCES CEREVISIAE 
saccharomyces cerevisiae solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2676
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) (SACCHAROMYCES CEREVISIAE - UNII:978D8U419H)	SACCHAROMYCES CEREVISIAE	20000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2676-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

SACCHAROMYCES CEREVISIAE 
saccharomyces cerevisiae solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2678
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) (SACCHAROMYCES CEREVISIAE - UNII:978D8U419H)	SACCHAROMYCES CEREVISIAE	40000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2678-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

SACCHAROMYCES CEREVISIAE 
saccharomyces cerevisiae solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5636
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) (SACCHAROMYCES CEREVISIAE - UNII:978D8U419H)	SACCHAROMYCES CEREVISIAE	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5636-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5636-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

STEMPHYLIUM SOLANI 
stemphylium solani solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2635
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
STEMPHYLIUM SOLANI (UNII: 1IEK4UDP5M) (STEMPHYLIUM SOLANI - UNII:1IEK4UDP5M)	STEMPHYLIUM SOLANI	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2635-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-2635-4	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	BLA101833	09/15/1981

STEMPHYLIUM SOLANI 
stemphylium solani solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2638
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
STEMPHYLIUM SOLANI (UNII: 1IEK4UDP5M) (STEMPHYLIUM SOLANI - UNII:1IEK4UDP5M)	STEMPHYLIUM SOLANI	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2638-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

TRICHOPHYTON MENTAGROPHYTES 
trichophyton mentagrophytes solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2649
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV)	TRICHOPHYTON MENTAGROPHYTES	40000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2649-4	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	BLA101833	09/15/1981

MUCOR CIRCINELLOIDES F. LUSITANICUS 
mucor circinelloides f. lusitanicus solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2659
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MUCOR CIRCINELLOIDES F. LUSITANICUS (UNII: 0J0X819B3C) (MUCOR CIRCINELLOIDES F. LUSITANICUS - UNII:0J0X819B3C)	MUCOR CIRCINELLOIDES F. LUSITANICUS	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2659-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

EPICOCCUM NIGRUM 
epicoccum nigrum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5616
Route of Administration	PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7)	EPICOCCUM NIGRUM	0.025 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5616-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2	NDC: 22840-5616-4	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	BLA101833	09/15/1981

EPIDERMOPHYTON FLOCCOSUM 
epidermophyton floccosum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5617
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EPIDERMOPHYTON FLOCCOSUM (UNII: 6JR6JTN25S) (EPIDERMOPHYTON FLOCCOSUM - UNII:6JR6JTN25S)	EPIDERMOPHYTON FLOCCOSUM	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5617-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5617-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-5617-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

MICROSPORUM CANIS 
microsporum canis solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5623
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MICROSPORUM CANIS (UNII: N4F4RQ7BY7) (MICROSPORUM CANIS - UNII:N4F4RQ7BY7)	MICROSPORUM CANIS	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5623-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5623-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-5623-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

BERMUDA GRASS SMUT 
ustilago cynodontis solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5648
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
USTILAGO CYNODONTIS (UNII: 0V3J4YEX2W) (USTILAGO CYNODONTIS - UNII:0V3J4YEX2W)	USTILAGO CYNODONTIS	0.025 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5648-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5648-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-5648-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

FUSARIUM MONILIFORME 
fusarium moniliforme solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1671
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2)	GIBBERELLA FUJIKUROI	20000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1671-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1671-4	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	BLA101833	09/15/1981

ASPERGILLUS AMSTELODAMI 
aspergillus amstelodami solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1608
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EUROTIUM AMSTELODAMI (UNII: D932NLL87Z) (EUROTIUM AMSTELODAMI - UNII:D932NLL87Z)	EUROTIUM AMSTELODAMI	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1608-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

ASPERGILLUS NIDULANS 
aspergillus nidulans solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5605
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS NIDULANS (UNII: 242A53RB80) (ASPERGILLUS NIDULANS - UNII:242A53RB80)	ASPERGILLUS NIDULANS	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5605-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

ASPERGILLUS NIGER 
aspergillus niger solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1626
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1626-4	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	BLA101833	09/15/1981

ASPERGILLUS NIGER 
aspergillus niger solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5606
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5606-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5606-5	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

CANDIDA ALBICANS 
candida albicans solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1644
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC)	CANDIDA ALBICANS	40000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1644-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1644-4	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	BLA101833	09/15/1981

EPICOCCUM NIGRUM 
epicoccum nigrum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1666
Route of Administration	PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7)	EPICOCCUM NIGRUM	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1666-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

ASPERGILLUS NIGER 
aspergillus niger solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1628
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1628-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

BIPOLARIS SOROKINIANA 
bipolaris sorokiniana solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1633
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W)	COCHLIOBOLUS SATIVUS	40000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1633-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1633-4	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	BLA101833	09/15/1981

DRECHSLERA SPICIFERA 
drechslera spicifera solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5615
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD)	COCHLIOBOLUS SPICIFER	0.025 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5615-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5615-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-5615-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

FUSARIUM SOLANI 
fusarium solani solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1676
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HAEMATONECTRIA HAEMATOCOCCA (UNII: 7TLR512M4A) (HAEMATONECTRIA HAEMATOCOCCA - UNII:7TLR512M4A)	HAEMATONECTRIA HAEMATOCOCCA	0.025 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1676-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

FUSARIUM SOLANI 
fusarium solani solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5619
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HAEMATONECTRIA HAEMATOCOCCA (UNII: 7TLR512M4A) (HAEMATONECTRIA HAEMATOCOCCA - UNII:7TLR512M4A)	HAEMATONECTRIA HAEMATOCOCCA	0.025 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5619-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5619-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

GLIOCLADIUM VIRIDE 
gliocladium viride solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1681
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLIOCLADIUM VIRIDE (UNII: 8Z8C642TPL) (GLIOCLADIUM VIRIDE - UNII:8Z8C642TPL)	GLIOCLADIUM VIRIDE	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1681-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1681-4	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	BLA101833	09/15/1981

GLIOCLADIUM VIRIDE 
gliocladium viride solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1682
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLIOCLADIUM VIRIDE (UNII: 8Z8C642TPL) (GLIOCLADIUM VIRIDE - UNII:8Z8C642TPL)	GLIOCLADIUM VIRIDE	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1682-4	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	BLA101833	09/15/1981

HELMINTHOSPORIUM SOLANI 
helminthosporium solani solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1691
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HELMINTHOSPORIUM SOLANI (UNII: U6Z259H815) (HELMINTHOSPORIUM SOLANI - UNII:U6Z259H815)	HELMINTHOSPORIUM SOLANI	40000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1691-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1691-4	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	BLA101833	09/15/1981

BOTRYTIS CINEREA 
botrytis cinerea solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-2662
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7)	BOTRYTIS CINEREA	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-2662-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

CLADOSPORIUM HERBARUM 
cladosporium herbarum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1653
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLADOSPORIUM HERBARUM (UNII: O64JF11198) (CLADOSPORIUM HERBARUM - UNII:O64JF11198)	CLADOSPORIUM HERBARUM	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1653-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1653-4	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	BLA101833	09/15/1981

CLADOSPORIUM HERBARUM 
cladosporium herbarum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1654
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLADOSPORIUM HERBARUM (UNII: O64JF11198) (CLADOSPORIUM HERBARUM - UNII:O64JF11198)	CLADOSPORIUM HERBARUM	20000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1654-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1654-4	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	BLA101833	09/15/1981

CLADOSPORIUM HERBARUM 
cladosporium herbarum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1656
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLADOSPORIUM HERBARUM (UNII: O64JF11198) (CLADOSPORIUM HERBARUM - UNII:O64JF11198)	CLADOSPORIUM HERBARUM	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1656-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

ALTERNARIA ALTERNATA 
alternaria alternata solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1605
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	10000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
PHENOL (UNII: 339NCG44TV)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1605-4	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	BLA101833	09/15/1981

ASPERGILLUS AMSTELODAMI 
aspergillus amstelodami solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1609
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EUROTIUM AMSTELODAMI (UNII: D932NLL87Z) (EUROTIUM AMSTELODAMI - UNII:D932NLL87Z)	EUROTIUM AMSTELODAMI	1000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1609-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

BOTRYTIS CINEREA 
botrytis cinerea solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1639
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7)	BOTRYTIS CINEREA	0.001 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1639-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

FUSARIUM MONILIFORME 
fusarium moniliforme solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1670
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2)	GIBBERELLA FUJIKUROI	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1670-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1670-4	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	BLA101833	09/15/1981

ASPERGILLUS FUMIGATUS 
aspergillus fumigatus solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1619
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48)	ASPERGILLUS FUMIGATUS	0.002 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1619-1	5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

ASPERGILLUS FLAVUS 
aspergillus flavus solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5603
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13)	ASPERGILLUS FLAVUS	0.025 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
PHENOL (UNII: 339NCG44TV)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5603-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5603-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-5603-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

BIPOLARIS SOROKINIANA 
bipolaris sorokiniana solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1634
Route of Administration	PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W)	COCHLIOBOLUS SATIVUS	20000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1634-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-1634-4	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	BLA101833	09/15/1981

CLADOSPORIUM HERBARUM 
cladosporium herbarum solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1657
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLADOSPORIUM HERBARUM (UNII: O64JF11198) (CLADOSPORIUM HERBARUM - UNII:O64JF11198)	CLADOSPORIUM HERBARUM	40000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1657-4	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	BLA101833	09/15/1981

CANDIDA ALBICANS 
candida albicans solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1640
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC)	CANDIDA ALBICANS	0.01 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1640-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

CANDIDA ALBICANS 
candida albicans solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-1642
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC)	CANDIDA ALBICANS	20000 [PNU]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-1642-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

ASPERGILLUS AMSTELODAMI 
aspergillus amstelodami solution

Product Information
Product Type	NON-STANDARDIZED ALLERGENIC	Item Code (Source)	NDC: 22840-5602
Route of Administration	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EUROTIUM AMSTELODAMI (UNII: D932NLL87Z) (EUROTIUM AMSTELODAMI - UNII:D932NLL87Z)	EUROTIUM AMSTELODAMI	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
PHENOL (UNII: 339NCG44TV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22840-5602-2	10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2	NDC: 22840-5602-4	50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3	NDC: 22840-5602-5	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA101833	09/15/1981

Labeler - Greer Laboratories, Inc. (024671414)

Registrant - Greer Laboratories, Inc. (024671414)

Establishment
Name	Address	ID/FEI	Business Operations
Greer Laboratories, Inc.		024671414	manufacture(22840-1100, 22840-1101, 22840-1102, 22840-1103, 22840-1105, 22840-1106, 22840-1107, 22840-1108, 22840-1110, 22840-1111, 22840-1112, 22840-1113, 22840-1116, 22840-1117, 22840-1118, 22840-1119, 22840-1121, 22840-1122, 22840-1123, 22840-1125, 22840-1126, 22840-1127, 22840-1128, 22840-1129, 22840-1130, 22840-1131, 22840-1133, 22840-1134, 22840-1135, 22840-1136, 22840-1138, 22840-1139, 22840-1140, 22840-1141, 22840-1142, 22840-1144, 22840-1145, 22840-1146, 22840-1147, 22840-1149, 22840-1150, 22840-1151, 22840-1153, 22840-1154, 22840-1155, 22840-1157, 22840-1159, 22840-1160, 22840-1162, 22840-1163, 22840-1164, 22840-1167, 22840-1168, 22840-1169, 22840-1170, 22840-1171, 22840-1173, 22840-1174, 22840-1175, 22840-1176, 22840-1537, 22840-1538, 22840-5100, 22840-5101, 22840-5102, 22840-5103, 22840-5104, 22840-5105, 22840-5106, 22840-5107, 22840-5108, 22840-5109, 22840-5110, 22840-5111, 22840-5112, 22840-5113, 22840-5114, 22840-5115, 22840-5517, 22840-9100, 22840-9101, 22840-9102, 22840-9103, 22840-9104, 22840-9105, 22840-9107)