ANIMAL ALLERGENS, AP HORSE HAIR AND DANDER- ap horse hair and dander injection, solution 
ANIMAL ALLERGENS, AP CATTLE HAIR AND DANDER- cattle hair and dander injection, solution 
ANIMAL ALLERGENS, FEATHER MIX- feather mix injection, solution 
INSECTS WHOLE BODY COCKROACH MIX- insects whole body cockroach mix injection, solution 
INSECTS WHOLE BODY, FIRE ANT MIX- insects whole body, fire ant mix injection, solution 
MOLDS - MOLD MIX 10- molds - mold mix 10 injection, solution 
MOLDS - MOLD MIX 4- molds - mold mix 4 injection, solution 
MOLDS - TRICHOPHYTON MIX- molds - trichophyton mix injection, solution 
MOLDS, PENICILLIUM MIX- molds, penicillium mix injection, solution 
MOLDS, RUSTS AND SMUTS, ALTERNARIA TENUIS- alternaria tenuis injection, solution 
MOLDS, RUSTS AND SMUTS, ASPERGILLUS FUMIGATUS- aspergillus fumigatus injection, solution 
MOLDS, RUSTS AND SMUTS, CANDIDA ALBICANS- candida albicans injection, solution 
MOLDS, RUSTS AND SMUTS, CEPHALOSPORIUM ACREMONIUM- cephalosporium acremonium injection, solution 
MOLDS, RUSTS AND SMUTS, CURVULARIA SPICIFERA- curvularia spicifera injection, solution 
MOLDS, RUSTS AND SMUTS, EPICOCCUM NIGRUM- epicoccum nigrum injection, solution 
MOLDS, RUSTS AND SMUTS, FUSARIUM VASINFECTUM- fusarium vasinfectum injection, solution 
MOLDS, RUSTS AND SMUTS, HELMINTHOSPORIUM INTERSEMINATUM- helminthosporium interseminatum injection, solution 
MOLDS, RUSTS AND SMUTS, HORMODENDRUM CLADOSPORIOIDES- hormodendrum cladosporioides injection, solution 
MOLDS, RUSTS AND SMUTS, MUCOR RACEMOSUS- mucor racemosus injection, solution 
MOLDS, RUSTS AND SMUTS, PENICILLIUM NOTATUM- penicillium notatum injection, solution 
MOLDS, RUSTS AND SMUTS, PHOMA HERBARUM- phoma herbarum injection, solution 
MOLDS, RUSTS AND SMUTS, PULLULARIA PULLULANS- pullularia pullulans injection, solution 
MOLDS, RUSTS AND SMUTS, RHIZOPUS NIGRICANS- rhizopus nigricans injection, solution 
MOLDS, RUSTS AND SMUTS, STEMPHYLIUM BOTRYOSUM- stemphylium botryosum injection, solution 
POLLENS - GRASSES, BAHIA GRASS PASPALUM NOTATUM- bahia grass paspalum notatum injection, solution 
POLLENS - GRASSES, JOHNSON GRASS SORGHUM HALEPENSE- johnson grass sorghum halepense injection, solution 
POLLENS - TREES, ACACIA ACACIA LONGIFOLIA- acacia longifolia injection, solution 
POLLENS - TREES, ALDER, RED ALNUS RUBRA- alder, red alnus rubra injection, solution 
POLLENS - TREES, ASH, WHITE FRAXINUS AMERICANA- ash, white fraxinus americana injection, solution 
POLLENS - TREES, BIRCH MIX- birch mix injection, solution 
POLLENS - TREES, BOXELDER/MAPLE MIX- boxelder/maple mix injection, solution 
POLLENS - TREES, CEDAR, MOUNTAIN JUNIPERUS ASHEI- cedar, mountain juniperus ashei injection, solution 
POLLENS - TREES, CEDAR, RED JUNIPERUS VIRGINIANA- cedar, red juniperus virginiana injection, solution 
POLLENS - TREES, COTTONWOOD, COMMON POPULUS DELTOIDES- cottonwood, common populus deltoides injection, solution 
POLLENS - TREES, ELM, AMERICAN ULMUS AMERICANA- elm, american ulmus americana injection, solution 
POLLENS - TREES, ELM, CHINESE ULMUS PARVIFOLIA- elm, chinese ulmus parvifolia injection, solution 
POLLENS - TREES, HACKBERRY CELTIS OCCIDENTALIS- hackberry celtis occidentalis injection, solution 
POLLENS - TREES, MAPLE, HARD ACER SACCHARUM- maple, hard acer saccharum injection, solution 
POLLENS - TREES, MESQUITE, PROSOPIS JULIFLORA- mesquite, prosopis juliflora injection, solution 
POLLENS - TREES, MULBERRY MIX- mulberry mix injection, solution 
POLLENS - TREES, OAK MIX- oak mix injection, solution 
POLLENS - TREES, OAK, RED QUERCUS RUBRA- oak, red quercus rubra injection, solution 
POLLENS - TREES, OLIVE OLEA EUROPAEA- olive olea europaea injection, solution 
POLLENS - TREES, PECAN CARYA CARYA ILLINOENSIS- pecan carya carya illinoensis injection, solution 
POLLENS - TREES, RUSSIAN OLIVE ELAEAGNUS ANGUSTIFOLIA- russian olive elaeagnus angustifolia injection, solution 
POLLENS - TREES, SYCAMORE, AMERICAN EASTERN PLATANUS OCCIDENTALLIS- sycamore, american eastern platanus occidentallis injection, solution 
POLLENS - TREES, TREE MIX 11- tree mix 11 injection, solution 
POLLENS - TREES, TREE MIX 5- tree mix 5 injection, solution 
POLLENS - TREES, TREE MIX 6- tree mix 6 injection, solution 
POLLENS - TREES, WALNUT, BLACK JUGLANS NIGRA- walnut, black juglans nigra injection, solution 
POLLENS - TREES, WILLOW, BLACK SALIX NIGRA- willow, black salix nigra injection, solution 
POLLENS - WEEDS AND GARDEN PLANTS, COCKLEBUR XANTHIUM STRUMARIUM- cocklebur xanthium strumarium injection, solution 
POLLENS - WEEDS AND GARDEN PLANTS, GOLDENROD SOLIDAGO CANADENSIS- goldenrod solidago canadensis injection, solution 
POLLENS - WEEDS AND GARDEN PLANTS, LAMB QUARTERS CHENOPODIUM ALBUM- lamb quarters chenopodium album injection, solution 
POLLENS - WEEDS AND GARDEN PLANTS, PIGWEED, ROUGH REDROOT AMARANTHUS RETROFLEXUS- pigweed, rough redroot amaranthus retroflexus injection, solution 
POLLENS - WEEDS AND GARDEN PLANTS, PLANTAIN, ENGLISH PLANTAGO LANCEOLATA- plantain, english plantago lanceolata injection, solution 
POLLENS - WEEDS AND GARDEN PLANTS, RAGWEED, GIANT AMBROSIA TRIFIDA- ragweed, giant ambrosia trifida injection, solution 
POLLENS - WEEDS AND GARDEN PLANTS, RAGWEED. WESTERN AMBROSIA PSILOSTACHYA- ragweed. western ambrosia psilostachya injection, solution 
POLLENS - WEEDS AND GARDEN PLANTS, RUSSIAN THISTLE SALSOLA KALI- russian thistle salsola kali injection, solution 
POLLENS - WEEDS AND GARDEN PLANTS, SAGEBRUSH, MUGWORT ARTEMISIA VULGARIS- sagebrush, mugwort artemisia vulgaris injection, solution 
POLLENS - WEEDS AND GARDEN PLANTS, SCALE, WING SHAD ATRIPLEX CANESCENS- scale, wing shad atriplex canescens injection, solution 
POLLENS - WEEDS, CARELESS/PIGWEED MIX- careless/pigweed mix injection, solution 
POLLENS - WEEDS, DOCK/SORREL MIX- pollens - weeds, dock/sorrel mix injection, solution 
POLLENS - WEEDS, GIANT, SHORT, WESTERN RAGWEED MIX- giant, short, western ragweed mix injection, solution 
POLLENS - WEEDS, KOCHIA SCOPARIA- kochia scoparia injection, solution 
POLLENS - WEEDS, MARSHELDER/POVERTY MIX- pollens - weeds, marshelder/poverty mix injection, solution 
POLLENS - WEEDS, WEED MIX 2630- weed mix 2630 injection, solution 
Jubilant HollisterStier LLC

----------

INSTRUCTIONS ALLERGENIC EXTRACTS FOR INTRADERMAL TESTING

WARNINGS

This product is intended for use only by licensed medical personnel experienced in administering allergenic extracts and trained to provide immediate emergency treatment in the event of a life-threatening reaction.

Allergenic extracts may potentially elicit a severe life-threatening systemic reaction, rarely resulting in death.7 Therefore, emergency measures and personnel trained in their use should be available immediately in the event of such a reaction. Patients should be instructed to recognize adverse reaction symptoms and cautioned to contact the physician's office if symptoms occur.

Scratch, prick or puncture test first. Test intradermally only to those antigens giving negative or questionable reactions on scratch, prick or puncture testing.

This product should never be injected intravenously.

Patients on non-selective beta blockers may be more reactive to allergens given for testing or treatment and may be unresponsive to the usual doses of epinephrine used to treat allergic reactions.6

Refer also to the WARNINGS, PRECAUTIONS, and ADVERSE REACTIONS Sections below for further discussion.

DESCRIPTION

Extracts for intradermal testing are supplied in sterile multi-dose vials containing, in addition to the extract allergens and antigens, 0.5% sodium chloride, 0.275% sodium bicarbonate, up to 2% glycerin, 2.5% glycerin for AP™ products, and, as preservative, 0.4% phenol. The strength of these extracts may be expressed in terms of: 

1. Weight to Volume (w/v)
2. Protein Nitrogen Units/mL (PNU/mL)
3. Allergy Units/mL (AU/mL)
4. Bioequivalent Allergy Units/mL (BAU/mL)
5. Concentrate

CLINICAL PHARMACOLOGY

Allergenic extracts for intradermal testing used according to the DOSAGE AND ADMINISTRATION Section, produce erythema or erythema and wheal reactions in patients with significant IgE-mediated sensitivity to the relevant allergen. This allergic inflammatory response, although not completely understood, is thought to begin with the reaction of antigen with IgE on the surface of basophils, or mast cells, which initiates a series of biochemical events resulting in the production of histamine, slow-reacting substance of anaphylaxis and other mediators. These, in turn, produce the immediate-type wheal and flare skin reaction.

INDICATIONS AND USAGE

Certain diagnostics carry labeling which states Allergenic Extract for Diagnostic Use Only. Data to support the therapeutic use of products labeled with this statement have not been established.15

In addition to a carefully taken history, the use of intradermal testing extracts is an accepted method in the diagnosis of allergenic conditions.1, 2, 3 When scratch, prick or puncture reactions are small, or if the patient gives a history of allergic symptoms to a substance but scratch, prick or puncture tests are inconclusive, intradermal tests may be indicated. However, ANTIGENS PRODUCING LARGE 3 TO 4+ SCRATCH, PRICK OR PUNCTURE TESTS SHOULD NOT BE TESTED INTRADERMALLY.

Extracts of all allergens do not produce equivalent results in intradermal testing. The intensity of the skin reaction produced will be determined by two factors: the degree of sensitivity of the patient and the nature of the antigenic extract applied. In general, pollen extracts produce whealing reactions, whereas other inhalants produce erythematous reactions with wheals less often. Skin tests to foods seldom produce whealing reactions except for infrequent instances of severe sensitivity to fish, nuts or spices, and rarely other foods.

CONTRAINDICATIONS

There are no known absolute contraindications to allergy skin testing. Patients with cardiovascular diseases or pulmonary diseases such as symptomatic asthma, and/or who are receiving cardiovascular drugs such as beta blockers, may be at higher risk for severe adverse reactions. These patients may also be more refractory to the normal anaphylaxis treatment regime.

WARNINGS

Scratch, prick or puncture test first. Test intradermally only to those antigens giving negative or questionable reactions on scratch, prick or puncture testing. Excessively large local reactions or systemic reactions are more likely to occur if the patient is skin tested shortly after exposure to large amounts of antigen to which he or she is sensitive. Therefore, use caution when applying pollen tests to patients during their active pollen season, or after an exposure to inhalant allergens that produce symptoms. Refer to boxed WARNINGS Section.

PRECAUTIONS

1. General

It is recommended that disposable syringes and needles are used for intradermal tests to prevent the possibility of accidental transfer of serum hepatitis and other infectious agents from one person to another. Always have injectable epinephrine and a tourniquet available when tests are being made. (See ADVERSE REACTION Section.) Patients should be observed in the office for 30 to 45 minutes after each set of intradermal tests and instructed to return to the office promptly if symptoms of an allergic reaction or shock occur. In order to avoid darkening and possible precipitation, do not dilute the following extracts with solutions containing phenol: Privet pollen and food extracts of White Potato, Corn, Oat, Rye, and Wheat. Injections of such extracts discolored by reaction with phenol may produce lasting tattoo-like discoloration of the skin.

2. Information for Patients

Patients should be instructed in the recognition of adverse reactions to diagnostic testing. Patients should be made to understand the importance of a 30 to 45 minute observation period and be warned to return to the office promptly if symptoms occur after leaving.

3. Carcinogenesis, Mutagensis, Impairment of Fertility

Long-term studies in animals have not been conducted with allergenic extracts to determine their potential for carcinogenicity, mutagenicity or impairment of fertility.

4. Pregnancy

4,5 Animal reproduction studies have not been conducted with allergenic extracts. It is also not known whether allergenic extracts can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Allergenic extracts should be given to a pregnant woman only if clearly needed.

5. Nursing Mothers

There are no current studies on secretion of the allergenic extract components in human milk or effect on the nursing infant. Because many drugs are excreted in human milk, caution should be exercised when allergenic extracts are administered to a nursing woman.

6. Drug Interactions

Patients on non-selective beta blockers may be more reactive to allergens given for testing or treatment and may be unresponsive to the usual doses of epinephrine used to treat allergic reactions.6
Certain medications may lessen the skin test wheal and erythema responses elicited by allergens and histamine for varying time periods. Conventional antihistamines should be discontinued at least 5 days before skin testing. Long acting antihistamines should be discontinued for at least 3 weeks prior to skin testing.10Topical steroids should be discontinued at the skin test site for at least 2-3 weeks before skin testing. 10, 11 Tricyclic antidepressants such as Doxepin should be withheld for at least 7 days before skin testing.12Topical local anesthetics may suppress the flare responses and should be avoided in skin test sites. 13

7. Geriatric Use

Skin test wheal size decreases with age. The decrease in allergeninduced skin test reaction parallels that to histamine; therefore, appropriate positive skin test controls should always be performed.1

8. Pediatric Use

Wheal sizes in response to allergen skin testing can be smaller in infants than in adults. The skin response to histamine parallels that for allergens; therefore, appropriate postitive control skin tests should always be performed.1

ADVERSE REACTIONS

1. Local Reactions

Large, persistent local reactions or minor exacerbations of the patient's allergic symptoms may be treated by local cold applications and/or the use of oral antihistamines, but they should be considered a warning of possible severe systemic reactions.

2. Systemic Reactions
With careful attention to dosage and administration, such reactions occur infrequently, but it must be remembered that allergenic extracts are highly potent in sensitive individuals and OVERDOSE could result in anaphylactic symptoms. Therefore, it is imperative that physicians administering allergenic extracts understand and be prepared for the treatment of severe reactions. Adverse reaction frequency data for allergenic extract administration for testing and treatment show that risk is low.7, 8 It cannot be overemphasized that, under certain unpredictable combinations of circumstances, anaphylactic shock is a possibility. Other possible systemic reaction symptoms, in varying degrees of severity, are fainting, pallor, bradycardia, hypotension, angioedema, cough, wheezing, conjunctivitis, rhinitis and urticaria. If a systemic or anaphylactic reaction does occur, apply a tourniquet above the site of injection, if tests are performed on the arms, and inject the 1:1000 epinephrine-hydrochloride intramuscularly or subcutaneously into the opposite arm. Loosen the tourniquet at least every 10 minutes. Do not obstruct arterial blood flow with the tourniquet.


EPINEPHRINE:

ADULT DOSAGE: 0.3 to 0.5 mL should be injected. Repeat in 5 to 10 minutes if necessary.
PEDIATRIC DOSAGE: The usual initial dose is 0.01 mg (mL) per kg body weight or 0.3 mg (mL) per square meter of body surface area. Suggested dosage for infants to 2 years of age is 0.05 mL to 0.1 mL; for children 2 to 6 years, 0.15 mL; and children 6 to 12 years, 0.2 mL. Single pediatric doses should not exceed 0.3 mg (mL). Doses may be repeated as frequently as every 20 minutes, depending on the severity of the condition and the response of the patient. After administration of epinephrine, profound shock or vasomotor collapse should be treated with intravenous fluids, and possibly vasoactive drugs. Oxygen should be given by mask. Intravenous antihistamine, theophylline or adrenal corticosteroids may be used if necessary after adequate epinephrine and circulatory support have been given. Emergency resuscitation measures and personnel trained in their use should be available immediately in the event of a serious systemic or anaphylactic reaction not responsive to the above measures. [Ref. J. Allergy Clin. Immunol. 77 (2): 271-273, 1986]. Rarely are all of the above measures necessary; the tourniquet and epinephrine usually produce prompt responses. However, the physician should be prepared in advance for all contingencies. Promptness in beginning emergency treatment measures is of utmost importance.

3. Adverse Event Reporting
Report all adverse events to Jubilant HollisterStier LLC Customer Technical Services Department at 1 (800) 992-1120. A voluntary adverse event reporting system for health professionals is available through the FDA MEDWATCH program. Preprinted forms (FDA Form 3500) are available from the FDA by calling 1 (800) FDA-1088. Completed forms should be mailed to MEDWATCH, 5600 Fisher Lane, Rockville, MD 20852-9787 or Fax to: 1 (800) FDA-0178.

OVERDOSE SECTION

See ADVERSE REACTIONS Section.

DOSAGE AND ADMINISTRATION

1. General

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

2. Intradermal Testing Methods
Cleanse the rubber stopper of the vial with liquid antiseptic before withdrawing extract. A sterile tuberculin syringe with 26-gauge, short-bevel needle should be used for the injection. The anterior surface of the upper and lower arm is preferable for testing. Cleanse the skin with soap and water or wash with alcohol or other antiseptic. Introduce the needle between the superficial layers of the skin and inject 0.02 mL of the extract. Test sites should be at least 2.5 cm apart, and no more than 10 to 20 antigens should be introduced at one time. This group can be followed with additional groups of 10, providing the reactions are not numerous or strong. The same amount of extract should be injected in each site for proper comparison. It is advisable to avoid testing with more than one allergen in the same group in each series, i.e., nuts, fish, epidermals, etc. A site should be injected with 0.02 mL of the control solution. All skin tests should be validated by appropriate positive control tests (e.g., histamine) and negative control tests [e.g., Glycerin, Albumin Saline with Phenol (0.4%), or Buffered Saline with Phenol (0.4%)]. The negative control test should be the same material as is used as a diluting fluid in the tested extracts. Diluting fluid is used in the same way as an active test extract. False positive reactions are sometimes encountered in intradermal testing, and the possibility of irritation reactions should always be taken into consideration. In cases where the patient is known to be quite sensitive, screen testing by scratch, prick or puncture method is recommended, and intradermal testing should be done with caution. The intradermal strength supplied is usually safe for testing patients presenting negative scratch, prick or puncture test reactions. It is recommended that a 1:10 dilution of the stock intradermal strength be used in preliminary testing of patients not previously screened by scratch, prick or puncture tests.

3. Use of Antigen Mixes
The use of complicated mixes of unrelated pollens for testing is not recommended since in the case of a positive reaction it does not indicate which pollen(s) are responsible, and in the case of a negative reaction, it fails to indicate whether the individual pollens at full concentration would give a positive reaction.

4. Reading Skin Test Reactions
A positive reaction consists of an urticarial wheal with surrounding erythema (resembling somewhat a mosquito bite reaction) larger than the control site. The smallest reaction considered positive is erythema with a central papule at least 5 mm in diameter. In some instances with no reaction at the control site, erythema may be considered an indication of sensitivity. In general, the size of wheal and erythema response correlates directly with the patient's sensitivity to that allergen.
Standardized Products
(a) Mites: The skin test concentrations of 30 AU/mL and 300 AU/mL in multiple dose vials are used for intradermal testing.
Intradermal skin test results in selected highly sensitive subjects are presented for reference purposes:

AU/mL that Elicited ∑E = 50 mm
Allergen
Number of
Persons
Mean
2 Std. Dev. Range
 D. farinae
 12
 0.0609
 0.0015-2.6016
 D. pteronyssinus
 12
 0.333
 0.0003-4.0077

Intradermal extracts should be used as follows:
(1) Patients with a negative scratch, prick or puncture test: Patients who do not react to a valid scratch, prick or puncture test should be tested intradermally with 0.02 to 0.05 mL of a 30 AU/mL extract solution. If this test is negative, a second intradermal test may be performed using a 300 AU/mL extract solution. The negative control used with this latter dilution should contain 0.5% glycerin.
(2) Patients tested only by the intradermal method: Patients suspected of being highly allergic should be tested with 0.02 to 0.05 mL of a solution containing 0.03 AU/mL. A negative test should be followed by repeat tests using progressively stronger concentrations until the maximum recommended strength of 300 AU/mL is reached. The negative control used with this latter dilution should contain 0.5% glycerin.
(b) Cat Hair and Cat Pelt: Intradermal endpoint titration (IET) tests were completed with Cat Pelt extract using 15 subjects to determine the mean concentration required to produce a ∑E of 50 (D50) mm.That concentration contained 0.042 BAU/mL (range 0.002 to 0.890 BAU/mL).
IET tests were completed with Cat Hair extract using 15 subjects to determine the mean concentration required to produce a ∑E of 50 mm (D50). That concentration contained 0.049 BAU/mL (range 0.006 to 0.661 BAU/mL).
Intradermal extract should be used as follows:
Intradermal Tests should be done only on patients with a negative prick or puncture test. Patients who do not react to a valid prick or puncture test should be tested intradermally with 0.02 to 0.05 mL of a 100 BAU/mL extract solution. If this test is negative, a second intradermal test may be performed using a 1,000 BAU/mL extract solution. If the intradermal dilutions were prepared from glycerinated concentrate, the negative control used with this latter dilution should contain 5% glycerin.
Standardized Cat Hair and Cat Pelt products are not interchangeable with each other or any other cat products including those labeled AU/mL.
(c) Ragweed pollen (Short Ragweed or Giant and Short Ragweed Mixture) Antigen E Assayed: The intradermal strength for Short Ragweed extract is usually 500 PNU, which by calculation contains approximately 0.7 to 3 units of Antigen E/mL. For Giant and Short Ragweed mix the suggested intradermal strength is 500 PNU, which by calculation contains 0.4 to 1.5 units of Antigen E/mL. These strengths are usually safe for testing patients previously having negative scratch, prick or puncture test reactions. A 1:10 dilution of the stock intradermal strength should be used in preliminary testing of patients not previously screened by scratch, prick, or puncture tests. A study of ragweed sensitive patients9 indicates that intradermal tests, using 0.05 mL of extract, produce positive reactions (1+ to 2+) at Antigen E concentrations of from 2.7x10 -1 to 2.7x10 -6 units per mL. The equivalent PNU range was 100 to 0.001 PNU per mL. Skin tests are graded in terms of the wheal and erythema response noted at 15 minutes. Wheal and erythema size may be recorded by actual measurement of the extent of both responses.

5. Geriatric Use

The dose is the same in patients of all age groups. Because the wheal size in response to allergen skin testing decreases with age, appropriate histamine positive control skin tests must be performed.1

6. Pediatric Use

The dose is the same in patients of all age groups. Wheal size in response to allergen skin testing can be smaller in infants than in adults. Appropriate histamine positive control skin tests must be performed.1

Refer to the following table to determine the skin test sensitivity grade. The corresponding ∑E (sum of the longest diameter and the mid-point orthogonal diameters of erythema) is also presented.

Grade
Erythema
mm
Papule or Wheal
mm
Coresponding
mm ∑E
 0
 <5
 <5
 <10
 ±
 5-10
 5-10
 10-20
 1+
 11-20
 5-10
 20-40
 2+
 21-30
 5-10
 40-60
 3+
 31-40
 10-15 (a)
 60-80
 4+
 >40
 >15 (b)
 > 80

a or with pseudopods

b or with many pseudopods

A positive skin reaction to any allergen must be interpreted in light of the patient’s history of symptoms, time of year, known exposures, and eating habits.
THE SKIN TESTS ARE IN NO WAY A SUBSTITUTE FOR A CAREFUL ALLERGENIC HISTORY; RATHER, THEY SERVE AS ADDITIONAL INFORMATION TO AID IN IDENTIFYING CAUSATIVE ALLERGENS IN PATIENTS WITH ALLERGIC DISORDERS.

HOW SUPPLIED

Most allergens are available in multiple dose 5 mL vials at PNU, w/v, some mixes as Concentrate, Standardized Mite products at AU/mL (30 AU/mL and 300 AU/mL each species), or Standardized Grass products at BAU/mL [100 BAU/mL and 1,000 BAU/mL (Bermuda 100 BAU/mL only)]. Product labels state vials are for intradermal testing and list strengths.

STORAGE

The expiration date of the diagnostic extracts is listed on the container label. The extract should be stored at 2° to 8°C, and kept at this temperature range during office use.

LIMITED WARRANTY

A number of factors beyond our control could reduce the efficacy of this product or even result in an ill effect following its use. These include storage and handling of the product after it leaves our hands, diagnosis, dosage, method of administration and biological differences in individual patients. Because of these factors, it is important that this product be stored properly, and that the directions be followed carefully during use. No warranty, express or implied, including any warranty of merchantability or fitness, is made. Representatives of the Company are not authorized to vary the terms or the contents of any printed labeling, including the package insert, for this product except by printed notice from the Company’s headquarters. The prescriber and user of this product must accept the terms hereof.

REFERENCES

1. Middleton, Elliott, Jr., C. E. Reed, E. F. Ellis (ed.) Allergy Principles and Practice. Vol. 1, C. V. Mosby. 1978.

2. Sheldon, J. M., R. C. Lovell, K. P. Mathews. A Manual of Clinical Allergy. W. B. Saunders, 1967.
3. Tuft, L., H. L. Mueller. Allergy in Children. W. B. Saunders. 1979.
4. DuBuske, L.M., C.J. Ling and A.L. Sheffer. Special problems regarding allergen immunotherapy. Immunol. Allergy. Clin. North Am. (USA). 12(1): 145-175, 1992.
5. Weinstein, A. M., D. B. Dubin, W. K. Podleski, L. L. Spector, R. S. Farr. Asthma and pregnancy. JAMA. 134(11): 1161-1165, 1979.
6. Jacobs, Robert L., Goeffrey W. Rake, Jr., et al. Potentiated anaphylaxis in patients with drug-induced beta-adrenergic blockade. J. Allergy Clin. Immunol. 68(2): 125-127, August 1981.
7. Lockey, Richard F., Linda M. Benedict, Paul C. Turkeltaub, Samuel C. Bukantz. Fatalities from immunotherapy (IT) and skin testing (ST). J. Allergy Clin. Immunol. 79(4): 660-677, 1987.
8. Turkeltaub, Paul C., Peter J. Gergen. The risk of adverse reactions from percutaneous prick-puncture allergen skin testing, venipuncture, and body measurements: Data from the second National Health and Nutrition Examination Survey 1976-80 (NHANES II). J. Allergy Clin. Immunol. 84(6): 886-890, Dec. 1989.
9. Norman, P. S., L. M. Lichtenstein, K. Ishizaka. Diagnostic tests in ragweed hay fever. J. Allergy Clin. Immunol. 52(4): 212-224, 1973.
10. Pipkorn, Ulf. Pharmacological influence of anti-allergic medication on In Vivo allergen testing. Allergy. 43: 81-86, 1988.
11. Andersson, M., U. Pipkorn. Inhibition of the dermal immediate allergic reaction through prolonged treatment with topical glucocorticosteroids. J. Allergy Clin. Immunol. 79(2): 345-349, February 1987.
12. Rao, Kamineni S., et al. Duration of suppressive effect of tricyclic anti-depressants on histamine induced wheal and flare reactions on human skin. J. Allergy Clin. Immunol. 82: 752-757, November 1988.
13. Pipkorn, Ulf, M. Andersson. Topical dermal anesthesia inhibits the flare but not the wheal response to allergen and histamine in the skin prick test. Clinical Allergy. 17: 307-311, 1987.
14. Turkeltaub, Paul C., C. Rastogi Suresh, Harold Baer. Office of Biologics Research and Review skin test method for evaluation of subject sensitivity to standardized allergenic extracts and for assignment of allergy units to reference preparations using the ID50EAL method (Intradermal Dilution for 50 mm Sum of Erythema Determines the Allergy Unit). Methods of the Allergenic Products Branch Office of Biologics Research and Review, FDA, Bethesda, MD 20892. Revised May 9, 1986.
15. Food and Drug Administration. Biological products; Allergenic extracts classified in Category IIIB; Final order; Revocation of licenses. Federal Register. 59(220):59228ff, November 16, 1994.
16. Griffith, I.J., Pollock, D.G. Klapper, B.L. Rogers, A.K. Nault., Sequence Polymorphism of Amb a I and Amb a II, the Major Allergens in Ambrosia artemisiifolia (Short Ragweed). Int. Arch. Allergy Apply. Immunol., 96: 296-304, 1991.


Example Vial Label
ANIMAL ALLERGENS, AP HORSE HAIR AND DANDER 
ap horse hair and dander injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-4857
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
EQUUS CABALLUS HAIR (UNII: 4F35XG0149) (EQUUS CABALLUS HAIR - UNII:4F35XG0149) EQUUS CABALLUS HAIR0.0005 g  in 1 mL
EQUUS CABALLUS DANDER (UNII: J81SZ18495) (EQUUS CABALLUS DANDER - UNII:J81SZ18495) EQUUS CABALLUS DANDER0.0005 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-4857-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388801/30/1978
ANIMAL ALLERGENS, AP CATTLE HAIR AND DANDER 
cattle hair and dander injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-4813
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BOS TAURUS HAIR (UNII: TOQ97Z8644) (BOS TAURUS HAIR - UNII:TOQ97Z8644) BOS TAURUS HAIR0.0005 g  in 1 mL
BOS TAURUS DANDER (UNII: C8VYS726O8) (BOS TAURUS DANDER - UNII:C8VYS726O8) BOS TAURUS DANDER0.0005 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-4813-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388801/30/1978
ANIMAL ALLERGENS, FEATHER MIX 
feather mix injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-4351
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GALLUS GALLUS FEATHER (UNII: 1FCM16V0FV) (GALLUS GALLUS FEATHER - UNII:1FCM16V0FV) GALLUS GALLUS FEATHER200 [PNU]  in 1 mL
ANSER ANSER FEATHER (UNII: 15XI414745) (ANSER ANSER FEATHER - UNII:15XI414745) ANSER ANSER FEATHER200 [PNU]  in 1 mL
ANAS PLATYRHYNCHOS FEATHER (UNII: 83B65P4796) (ANAS PLATYRHYNCHOS FEATHER - UNII:83B65P4796) ANAS PLATYRHYNCHOS FEATHER200 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-4351-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
INSECTS WHOLE BODY COCKROACH MIX 
insects whole body cockroach mix injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-6586
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (PERIPLANETA AMERICANA - UNII:2RQ1L9N089) PERIPLANETA AMERICANA500 [PNU]  in 1 mL
BLATELLA GERMANICA (UNII: G9O67I0A8Q) (BLATELLA GERMANICA - UNII:G9O67I0A8Q) BLATELLA GERMANICA500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-6586-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
INSECTS WHOLE BODY, FIRE ANT MIX 
insects whole body, fire ant mix injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-6516
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SOLENOPSIS RICHTERI (UNII: 739684T11W) (SOLENOPSIS RICHTERI - UNII:739684T11W) SOLENOPSIS RICHTERI500 [PNU]  in 1 mL
SOLENOPSIS INVICTA (UNII: 5O7CR4P444) (SOLENOPSIS INVICTA - UNII:5O7CR4P444) SOLENOPSIS INVICTA500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-6516-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
MOLDS - MOLD MIX 10 
molds - mold mix 10 injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5138
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA1000 [PNU]  in 1 mL
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS1000 [PNU]  in 1 mL
ASPERGILLUS NIDULANS (UNII: 242A53RB80) (ASPERGILLUS NIDULANS - UNII:242A53RB80) ASPERGILLUS NIDULANS1000 [PNU]  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER1000 [PNU]  in 1 mL
ASPERGILLUS TERREUS (UNII: QBN8K7055X) (ASPERGILLUS TERREUS - UNII:QBN8K7055X) ASPERGILLUS TERREUS1000 [PNU]  in 1 mL
FUSARIUM OXYSPORUM VASINFECTUM (UNII: 6M98DC08TZ) (FUSARIUM OXYSPORUM VASINFECTUM - UNII:6M98DC08TZ) FUSARIUM OXYSPORUM VASINFECTUM1000 [PNU]  in 1 mL
DENDRYPHIELLA VINOSA (UNII: 7S6NW5FH8X) (DENDRYPHIELLA VINOSA - UNII:7S6NW5FH8X) DENDRYPHIELLA VINOSA1000 [PNU]  in 1 mL
CLADOSPORIUM CLADOSPORIOIDES (UNII: 4ZWY20GTGO) (CLADOSPORIUM CLADOSPORIOIDES - UNII:4ZWY20GTGO) CLADOSPORIUM CLADOSPORIOIDES1000 [PNU]  in 1 mL
MUCOR RACEMOSUS (UNII: 17RH99LQ7G) (MUCOR RACEMOSUS - UNII:17RH99LQ7G) MUCOR RACEMOSUS1000 [PNU]  in 1 mL
PENICILLIUM DIGITATUM (UNII: 1SB49SV239) (PENICILLIUM DIGITATUM - UNII:1SB49SV239) PENICILLIUM DIGITATUM1000 [PNU]  in 1 mL
PENICILLIUM EXPANSUM (UNII: 1XSC3BB35Z) (PENICILLIUM EXPANSUM - UNII:1XSC3BB35Z) PENICILLIUM EXPANSUM1000 [PNU]  in 1 mL
PENICILLIUM GLAUCUM (UNII: E3X33F517C) (PENICILLIUM GLAUCUM - UNII:E3X33F517C) PENICILLIUM GLAUCUM1000 [PNU]  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM1000 [PNU]  in 1 mL
CLONOSTACHYS ROSEA F. ROSEA (UNII: I5F729WZ2H) (CLONOSTACHYS ROSEA F. ROSEA - UNII:I5F729WZ2H) CLONOSTACHYS ROSEA F. ROSEA1000 [PNU]  in 1 mL
PHOMA EXIGUA VAR. EXIGUA (UNII: 8JAG41IE4M) (PHOMA EXIGUA VAR. EXIGUA - UNII:8JAG41IE4M) PHOMA EXIGUA VAR. EXIGUA1000 [PNU]  in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS1000 [PNU]  in 1 mL
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER1000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-5138-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
MOLDS - MOLD MIX 4 
molds - mold mix 4 injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5001
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA1000 [PNU]  in 1 mL
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS1000 [PNU]  in 1 mL
ASPERGILLUS NIDULANS (UNII: 242A53RB80) (ASPERGILLUS NIDULANS - UNII:242A53RB80) ASPERGILLUS NIDULANS1000 [PNU]  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER1000 [PNU]  in 1 mL
ASPERGILLUS TERREUS (UNII: QBN8K7055X) (ASPERGILLUS TERREUS - UNII:QBN8K7055X) ASPERGILLUS TERREUS1000 [PNU]  in 1 mL
CLADOSPORIUM CLADOSPORIOIDES (UNII: 4ZWY20GTGO) (CLADOSPORIUM CLADOSPORIOIDES - UNII:4ZWY20GTGO) CLADOSPORIUM CLADOSPORIOIDES1000 [PNU]  in 1 mL
PENICILLIUM DIGITATUM (UNII: 1SB49SV239) (PENICILLIUM DIGITATUM - UNII:1SB49SV239) PENICILLIUM DIGITATUM1000 [PNU]  in 1 mL
PENICILLIUM EXPANSUM (UNII: 1XSC3BB35Z) (PENICILLIUM EXPANSUM - UNII:1XSC3BB35Z) PENICILLIUM EXPANSUM1000 [PNU]  in 1 mL
PENICILLIUM GLAUCUM (UNII: E3X33F517C) (PENICILLIUM GLAUCUM - UNII:E3X33F517C) PENICILLIUM GLAUCUM1000 [PNU]  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM1000 [PNU]  in 1 mL
CLONOSTACHYS ROSEA F. ROSEA (UNII: I5F729WZ2H) (CLONOSTACHYS ROSEA F. ROSEA - UNII:I5F729WZ2H) CLONOSTACHYS ROSEA F. ROSEA1000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-5001-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
MOLDS - TRICHOPHYTON MIX 
molds - trichophyton mix injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5286
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICHOPHYTON TONSURANS (UNII: JY1BE33I3Y) (TRICHOPHYTON TONSURANS - UNII:JY1BE33I3Y) TRICHOPHYTON TONSURANS1000 [PNU]  in 1 mL
TRICHOPHYTON RUBRUM (UNII: 2ZAU32517N) (TRICHOPHYTON RUBRUM - UNII:2ZAU32517N) TRICHOPHYTON RUBRUM1000 [PNU]  in 1 mL
TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV) TRICHOPHYTON MENTAGROPHYTES1000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-5286-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
MOLDS, PENICILLIUM MIX 
molds, penicillium mix injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5170
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PENICILLIUM DIGITATUM (UNII: 1SB49SV239) (PENICILLIUM DIGITATUM - UNII:1SB49SV239) PENICILLIUM DIGITATUM1000 [PNU]  in 1 mL
PENICILLIUM EXPANSUM (UNII: 1XSC3BB35Z) (PENICILLIUM EXPANSUM - UNII:1XSC3BB35Z) PENICILLIUM EXPANSUM1000 [PNU]  in 1 mL
PENICILLIUM GLAUCUM (UNII: E3X33F517C) (PENICILLIUM GLAUCUM - UNII:E3X33F517C) PENICILLIUM GLAUCUM1000 [PNU]  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM1000 [PNU]  in 1 mL
CLONOSTACHYS ROSEA F. ROSEA (UNII: I5F729WZ2H) (CLONOSTACHYS ROSEA F. ROSEA - UNII:I5F729WZ2H) CLONOSTACHYS ROSEA F. ROSEA1000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-5170-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
MOLDS, RUSTS AND SMUTS, ALTERNARIA TENUIS 
alternaria tenuis injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5010
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA1000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-5010-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
MOLDS, RUSTS AND SMUTS, ASPERGILLUS FUMIGATUS 
aspergillus fumigatus injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5022
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS1000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-5022-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
MOLDS, RUSTS AND SMUTS, CANDIDA ALBICANS 
candida albicans injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5054
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS1000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-5054-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
MOLDS, RUSTS AND SMUTS, CEPHALOSPORIUM ACREMONIUM 
cephalosporium acremonium injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5058
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SAROCLADIUM STRICTUM (UNII: 3F36V0451W) (SAROCLADIUM STRICTUM - UNII:3F36V0451W) SAROCLADIUM STRICTUM1000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-5058-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
MOLDS, RUSTS AND SMUTS, CURVULARIA SPICIFERA 
curvularia spicifera injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5078
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD) COCHLIOBOLUS SPICIFER1000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-5078-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
MOLDS, RUSTS AND SMUTS, EPICOCCUM NIGRUM 
epicoccum nigrum injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5102
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM1000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-5102-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
MOLDS, RUSTS AND SMUTS, FUSARIUM VASINFECTUM 
fusarium vasinfectum injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5114
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FUSARIUM OXYSPORUM VASINFECTUM (UNII: 6M98DC08TZ) (FUSARIUM OXYSPORUM VASINFECTUM - UNII:6M98DC08TZ) FUSARIUM OXYSPORUM VASINFECTUM1000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-5114-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
MOLDS, RUSTS AND SMUTS, HELMINTHOSPORIUM INTERSEMINATUM 
helminthosporium interseminatum injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5126
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DENDRYPHIELLA VINOSA (UNII: 7S6NW5FH8X) (DENDRYPHIELLA VINOSA - UNII:7S6NW5FH8X) DENDRYPHIELLA VINOSA1000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-5126-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
MOLDS, RUSTS AND SMUTS, HORMODENDRUM CLADOSPORIOIDES 
hormodendrum cladosporioides injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5130
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CLADOSPORIUM CLADOSPORIOIDES (UNII: 4ZWY20GTGO) (CLADOSPORIUM CLADOSPORIOIDES - UNII:4ZWY20GTGO) CLADOSPORIUM CLADOSPORIOIDES1000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-5130-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
MOLDS, RUSTS AND SMUTS, MUCOR RACEMOSUS 
mucor racemosus injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5146
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MUCOR RACEMOSUS (UNII: 17RH99LQ7G) (MUCOR RACEMOSUS - UNII:17RH99LQ7G) MUCOR RACEMOSUS1000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-5146-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
MOLDS, RUSTS AND SMUTS, PENICILLIUM NOTATUM 
penicillium notatum injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5210
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM1000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-5210-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
MOLDS, RUSTS AND SMUTS, PHOMA HERBARUM 
phoma herbarum injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5222
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PHOMA EXIGUA VAR. EXIGUA (UNII: 8JAG41IE4M) (PHOMA EXIGUA VAR. EXIGUA - UNII:8JAG41IE4M) PHOMA EXIGUA VAR. EXIGUA1000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-5222-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
MOLDS, RUSTS AND SMUTS, PULLULARIA PULLULANS 
pullularia pullulans injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5234
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS1000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-5234-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
MOLDS, RUSTS AND SMUTS, RHIZOPUS NIGRICANS 
rhizopus nigricans injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5231
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER1000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-5231-15 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
MOLDS, RUSTS AND SMUTS, STEMPHYLIUM BOTRYOSUM 
stemphylium botryosum injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5266
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PLEOSPORA TARDA (UNII: TPL549N9R8) (PLEOSPORA TARDA - UNII:TPL549N9R8) PLEOSPORA TARDA1000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-5266-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - GRASSES, BAHIA GRASS PASPALUM NOTATUM 
bahia grass paspalum notatum injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1083
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK) (PASPALUM NOTATUM POLLEN - UNII:V003SHB7VK) PASPALUM NOTATUM POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-1083-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - GRASSES, JOHNSON GRASS SORGHUM HALEPENSE 
johnson grass sorghum halepense injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1746
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP) (SORGHUM HALEPENSE POLLEN - UNII:577VA5B4HP) SORGHUM HALEPENSE POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-1746-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - TREES, ACACIA ACACIA LONGIFOLIA 
acacia longifolia injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1008
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACACIA LONGIFOLIA POLLEN (UNII: 24SO2J296O) (ACACIA LONGIFOLIA POLLEN - UNII:24SO2J296O) ACACIA LONGIFOLIA POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-1008-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - TREES, ALDER, RED ALNUS RUBRA 
alder, red alnus rubra injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1020
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALNUS RUBRA POLLEN (UNII: Z0F2YK1B7H) (ALNUS RUBRA POLLEN - UNII:Z0F2YK1B7H) ALNUS RUBRA POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-1020-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - TREES, ASH, WHITE FRAXINUS AMERICANA 
ash, white fraxinus americana injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1062
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q) (FRAXINUS AMERICANA POLLEN - UNII:G684LX721Q) FRAXINUS AMERICANA POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-1062-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - TREES, BIRCH MIX 
birch mix injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1170
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BETULA PAPYRIFERA POLLEN (UNII: 3538FNV8AY) (BETULA PAPYRIFERA POLLEN - UNII:3538FNV8AY) BETULA PAPYRIFERA POLLEN500 [PNU]  in 1 mL
BETULA PENDULA POLLEN (UNII: ZL5TV40C5Y) (BETULA PENDULA POLLEN - UNII:ZL5TV40C5Y) BETULA PENDULA POLLEN500 [PNU]  in 1 mL
BETULA NIGRA POLLEN (UNII: 93963RFO1P) (BETULA NIGRA POLLEN - UNII:93963RFO1P) BETULA NIGRA POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-1170-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - TREES, BOXELDER/MAPLE MIX 
boxelder/maple mix injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1215
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACER NEGUNDO POLLEN (UNII: P6K070AR8V) (ACER NEGUNDO POLLEN - UNII:P6K070AR8V) ACER NEGUNDO POLLEN500 [PNU]  in 1 mL
ACER SACCHARUM POLLEN (UNII: V38QUQ7861) (ACER SACCHARUM POLLEN - UNII:V38QUQ7861) ACER SACCHARUM POLLEN500 [PNU]  in 1 mL
ACER RUBRUM POLLEN (UNII: 700NK45C76) (ACER RUBRUM POLLEN - UNII:700NK45C76) ACER RUBRUM POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-1215-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - TREES, CEDAR, MOUNTAIN JUNIPERUS ASHEI 
cedar, mountain juniperus ashei injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1338
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
JUNIPERUS ASHEI POLLEN (UNII: 544F8MEY0Y) (JUNIPERUS ASHEI POLLEN - UNII:544F8MEY0Y) JUNIPERUS ASHEI POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-1338-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - TREES, CEDAR, RED JUNIPERUS VIRGINIANA 
cedar, red juniperus virginiana injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1341
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
JUNIPERUS VIRGINIANA POLLEN (UNII: PY0JA16R2G) (JUNIPERUS VIRGINIANA POLLEN - UNII:PY0JA16R2G) JUNIPERUS VIRGINIANA POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-1341-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - TREES, COTTONWOOD, COMMON POPULUS DELTOIDES 
cottonwood, common populus deltoides injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1437
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POPULUS DELTOIDES POLLEN (UNII: 476DVV63WP) (POPULUS DELTOIDES POLLEN - UNII:476DVV63WP) POPULUS DELTOIDES POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-1437-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - TREES, ELM, AMERICAN ULMUS AMERICANA 
elm, american ulmus americana injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1542
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ULMUS AMERICANA POLLEN (UNII: 89BAT511BD) (ULMUS AMERICANA POLLEN - UNII:89BAT511BD) ULMUS AMERICANA POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-1542-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - TREES, ELM, CHINESE ULMUS PARVIFOLIA 
elm, chinese ulmus parvifolia injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1548
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ULMUS PARVIFOLIA POLLEN (UNII: IU0Z41653U) (ULMUS PARVIFOLIA POLLEN - UNII:IU0Z41653U) ULMUS PARVIFOLIA POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-1548-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - TREES, HACKBERRY CELTIS OCCIDENTALIS 
hackberry celtis occidentalis injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1665
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CELTIS OCCIDENTALIS POLLEN (UNII: 68R9X9Y96X) (CELTIS OCCIDENTALIS POLLEN - UNII:68R9X9Y96X) CELTIS OCCIDENTALIS POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-1665-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - TREES, MAPLE, HARD ACER SACCHARUM 
maple, hard acer saccharum injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1833
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACER SACCHARUM POLLEN (UNII: V38QUQ7861) (ACER SACCHARUM POLLEN - UNII:V38QUQ7861) ACER SACCHARUM POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-1833-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - TREES, MESQUITE, PROSOPIS JULIFLORA 
mesquite, prosopis juliflora injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1878
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PROSOPIS JULIFLORA POLLEN (UNII: 6EIJ3D04MR) (PROSOPIS JULIFLORA POLLEN - UNII:6EIJ3D04MR) PROSOPIS JULIFLORA POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-1878-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - TREES, MULBERRY MIX 
mulberry mix injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1911
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MORUS ALBA POLLEN (UNII: 3I9T68187H) (MORUS ALBA POLLEN - UNII:3I9T68187H) MORUS ALBA POLLEN500 [PNU]  in 1 mL
MORUS RUBRA POLLEN (UNII: 9LYI4RTZ52) (MORUS RUBRA POLLEN - UNII:9LYI4RTZ52) MORUS RUBRA POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-1911-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - TREES, OAK MIX 
oak mix injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2037
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
QUERCUS RUBRA POLLEN (UNII: SVW19ET93C) (QUERCUS RUBRA POLLEN - UNII:SVW19ET93C) QUERCUS RUBRA POLLEN500 [PNU]  in 1 mL
QUERCUS VIRGINIANA POLLEN (UNII: 8KDG09A4GO) (QUERCUS VIRGINIANA POLLEN - UNII:8KDG09A4GO) QUERCUS VIRGINIANA POLLEN500 [PNU]  in 1 mL
QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK) (QUERCUS ALBA POLLEN - UNII:Z4Y9ZSV4KK) QUERCUS ALBA POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-2037-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - TREES, OAK, RED QUERCUS RUBRA 
oak, red quercus rubra injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2016
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
QUERCUS RUBRA POLLEN (UNII: SVW19ET93C) (QUERCUS RUBRA POLLEN - UNII:SVW19ET93C) QUERCUS RUBRA POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-2016-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - TREES, OLIVE OLEA EUROPAEA 
olive olea europaea injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2052
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OLEA EUROPAEA POLLEN (UNII: 43R41XZ627) (OLEA EUROPAEA POLLEN - UNII:43R41XZ627) OLEA EUROPAEA POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-2052-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - TREES, PECAN CARYA CARYA ILLINOENSIS 
pecan carya carya illinoensis injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2100
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARYA ILLINOINENSIS POLLEN (UNII: PYO4JR720Y) (CARYA ILLINOINENSIS POLLEN - UNII:PYO4JR720Y) CARYA ILLINOINENSIS POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-2100-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - TREES, RUSSIAN OLIVE ELAEAGNUS ANGUSTIFOLIA 
russian olive elaeagnus angustifolia injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2361
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ELAEAGNUS ANGUSTIFOLIA POLLEN (UNII: 68P4F4M6VD) (ELAEAGNUS ANGUSTIFOLIA POLLEN - UNII:68P4F4M6VD) ELAEAGNUS ANGUSTIFOLIA POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-2361-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - TREES, SYCAMORE, AMERICAN EASTERN PLATANUS OCCIDENTALLIS 
sycamore, american eastern platanus occidentallis injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2565
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PLATANUS OCCIDENTALIS POLLEN (UNII: E03U1K03LK) (PLATANUS OCCIDENTALIS POLLEN - UNII:E03U1K03LK) PLATANUS OCCIDENTALIS POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-2565-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - TREES, TREE MIX 11 
tree mix 11 injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2621
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q) (FRAXINUS AMERICANA POLLEN - UNII:G684LX721Q) FRAXINUS AMERICANA POLLEN500 [PNU]  in 1 mL
FAGUS GRANDIFOLIA POLLEN (UNII: 34X886W1H4) (FAGUS GRANDIFOLIA POLLEN - UNII:34X886W1H4) FAGUS GRANDIFOLIA POLLEN500 [PNU]  in 1 mL
BETULA NIGRA POLLEN (UNII: 93963RFO1P) (BETULA NIGRA POLLEN - UNII:93963RFO1P) BETULA NIGRA POLLEN500 [PNU]  in 1 mL
JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (JUGLANS NIGRA POLLEN - UNII:1BV28146ZR) JUGLANS NIGRA POLLEN500 [PNU]  in 1 mL
POPULUS DELTOIDES POLLEN (UNII: 476DVV63WP) (POPULUS DELTOIDES POLLEN - UNII:476DVV63WP) POPULUS DELTOIDES POLLEN500 [PNU]  in 1 mL
ULMUS AMERICANA POLLEN (UNII: 89BAT511BD) (ULMUS AMERICANA POLLEN - UNII:89BAT511BD) ULMUS AMERICANA POLLEN500 [PNU]  in 1 mL
CARYA OVATA POLLEN (UNII: 54UN9R2798) (CARYA OVATA POLLEN - UNII:54UN9R2798) CARYA OVATA POLLEN500 [PNU]  in 1 mL
ACER SACCHARUM POLLEN (UNII: V38QUQ7861) (ACER SACCHARUM POLLEN - UNII:V38QUQ7861) ACER SACCHARUM POLLEN500 [PNU]  in 1 mL
QUERCUS RUBRA POLLEN (UNII: SVW19ET93C) (QUERCUS RUBRA POLLEN - UNII:SVW19ET93C) QUERCUS RUBRA POLLEN500 [PNU]  in 1 mL
PLATANUS OCCIDENTALIS POLLEN (UNII: E03U1K03LK) (PLATANUS OCCIDENTALIS POLLEN - UNII:E03U1K03LK) PLATANUS OCCIDENTALIS POLLEN500 [PNU]  in 1 mL
SALIX NIGRA POLLEN (UNII: 6M2JIH93ZN) (SALIX NIGRA POLLEN - UNII:6M2JIH93ZN) SALIX NIGRA POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-2621-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - TREES, TREE MIX 5 
tree mix 5 injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2857
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARYA ILLINOINENSIS POLLEN (UNII: PYO4JR720Y) (CARYA ILLINOINENSIS POLLEN - UNII:PYO4JR720Y) CARYA ILLINOINENSIS POLLEN500 [PNU]  in 1 mL
ACER SACCHARUM POLLEN (UNII: V38QUQ7861) (ACER SACCHARUM POLLEN - UNII:V38QUQ7861) ACER SACCHARUM POLLEN500 [PNU]  in 1 mL
ACER NEGUNDO POLLEN (UNII: P6K070AR8V) (ACER NEGUNDO POLLEN - UNII:P6K070AR8V) ACER NEGUNDO POLLEN500 [PNU]  in 1 mL
ACER RUBRUM POLLEN (UNII: 700NK45C76) (ACER RUBRUM POLLEN - UNII:700NK45C76) ACER RUBRUM POLLEN500 [PNU]  in 1 mL
QUERCUS RUBRA POLLEN (UNII: SVW19ET93C) (QUERCUS RUBRA POLLEN - UNII:SVW19ET93C) QUERCUS RUBRA POLLEN500 [PNU]  in 1 mL
QUERCUS VIRGINIANA POLLEN (UNII: 8KDG09A4GO) (QUERCUS VIRGINIANA POLLEN - UNII:8KDG09A4GO) QUERCUS VIRGINIANA POLLEN500 [PNU]  in 1 mL
QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK) (QUERCUS ALBA POLLEN - UNII:Z4Y9ZSV4KK) QUERCUS ALBA POLLEN500 [PNU]  in 1 mL
PLATANUS OCCIDENTALIS POLLEN (UNII: E03U1K03LK) (PLATANUS OCCIDENTALIS POLLEN - UNII:E03U1K03LK) PLATANUS OCCIDENTALIS POLLEN500 [PNU]  in 1 mL
SALIX NIGRA POLLEN (UNII: 6M2JIH93ZN) (SALIX NIGRA POLLEN - UNII:6M2JIH93ZN) SALIX NIGRA POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-2857-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - TREES, TREE MIX 6 
tree mix 6 injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2860
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q) (FRAXINUS AMERICANA POLLEN - UNII:G684LX721Q) FRAXINUS AMERICANA POLLEN500 [PNU]  in 1 mL
FAGUS GRANDIFOLIA POLLEN (UNII: 34X886W1H4) (FAGUS GRANDIFOLIA POLLEN - UNII:34X886W1H4) FAGUS GRANDIFOLIA POLLEN500 [PNU]  in 1 mL
BETULA PAPYRIFERA POLLEN (UNII: 3538FNV8AY) (BETULA PAPYRIFERA POLLEN - UNII:3538FNV8AY) BETULA PAPYRIFERA POLLEN500 [PNU]  in 1 mL
BETULA NIGRA POLLEN (UNII: 93963RFO1P) (BETULA NIGRA POLLEN - UNII:93963RFO1P) BETULA NIGRA POLLEN500 [PNU]  in 1 mL
BETULA PENDULA POLLEN (UNII: ZL5TV40C5Y) (BETULA PENDULA POLLEN - UNII:ZL5TV40C5Y) BETULA PENDULA POLLEN500 [PNU]  in 1 mL
JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (JUGLANS NIGRA POLLEN - UNII:1BV28146ZR) JUGLANS NIGRA POLLEN500 [PNU]  in 1 mL
POPULUS DELTOIDES POLLEN (UNII: 476DVV63WP) (POPULUS DELTOIDES POLLEN - UNII:476DVV63WP) POPULUS DELTOIDES POLLEN500 [PNU]  in 1 mL
ULMUS AMERICANA POLLEN (UNII: 89BAT511BD) (ULMUS AMERICANA POLLEN - UNII:89BAT511BD) ULMUS AMERICANA POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-2860-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - TREES, WALNUT, BLACK JUGLANS NIGRA 
walnut, black juglans nigra injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2628
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (JUGLANS NIGRA POLLEN - UNII:1BV28146ZR) JUGLANS NIGRA POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-2628-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - TREES, WILLOW, BLACK SALIX NIGRA 
willow, black salix nigra injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2679
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALIX NIGRA POLLEN (UNII: 6M2JIH93ZN) (SALIX NIGRA POLLEN - UNII:6M2JIH93ZN) SALIX NIGRA POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-2679-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - WEEDS AND GARDEN PLANTS, COCKLEBUR XANTHIUM STRUMARIUM 
cocklebur xanthium strumarium injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1407
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
XANTHIUM STRUMARIUM POLLEN (UNII: 2QOF601J1M) (XANTHIUM STRUMARIUM POLLEN - UNII:2QOF601J1M) XANTHIUM STRUMARIUM POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-1407-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - WEEDS AND GARDEN PLANTS, GOLDENROD SOLIDAGO CANADENSIS 
goldenrod solidago canadensis injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1632
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SOLIDAGO CANADENSIS POLLEN (UNII: 644CZ16IR5) (SOLIDAGO CANADENSIS POLLEN - UNII:644CZ16IR5) SOLIDAGO CANADENSIS POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-1632-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - WEEDS AND GARDEN PLANTS, LAMB QUARTERS CHENOPODIUM ALBUM 
lamb quarters chenopodium album injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1788
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN) (CHENOPODIUM ALBUM POLLEN - UNII:098LKX5NCN) CHENOPODIUM ALBUM POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-1788-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - WEEDS AND GARDEN PLANTS, PIGWEED, ROUGH REDROOT AMARANTHUS RETROFLEXUS 
pigweed, rough redroot amaranthus retroflexus injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2127
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW) (AMARANTHUS RETROFLEXUS POLLEN - UNII:73B14PX5FW) AMARANTHUS RETROFLEXUS POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-2127-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - WEEDS AND GARDEN PLANTS, PLANTAIN, ENGLISH PLANTAGO LANCEOLATA 
plantain, english plantago lanceolata injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2214
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI) (PLANTAGO LANCEOLATA POLLEN - UNII:DO87T1U2CI) PLANTAGO LANCEOLATA POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-2214-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - WEEDS AND GARDEN PLANTS, RAGWEED, GIANT AMBROSIA TRIFIDA 
ragweed, giant ambrosia trifida injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2295
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AMBROSIA TRIFIDA POLLEN (UNII: KU1V1898XX) (AMBROSIA TRIFIDA POLLEN - UNII:KU1V1898XX) AMBROSIA TRIFIDA POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-2295-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - WEEDS AND GARDEN PLANTS, RAGWEED. WESTERN AMBROSIA PSILOSTACHYA 
ragweed. western ambrosia psilostachya injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2310
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AMBROSIA PSILOSTACHYA POLLEN (UNII: RX18M46K8L) (AMBROSIA PSILOSTACHYA POLLEN - UNII:RX18M46K8L) AMBROSIA PSILOSTACHYA POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-2310-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - WEEDS AND GARDEN PLANTS, RUSSIAN THISTLE SALSOLA KALI 
russian thistle salsola kali injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2364
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALSOLA KALI POLLEN (UNII: 2MH135KC6G) (SALSOLA KALI POLLEN - UNII:2MH135KC6G) SALSOLA KALI POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-2364-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - WEEDS AND GARDEN PLANTS, SAGEBRUSH, MUGWORT ARTEMISIA VULGARIS 
sagebrush, mugwort artemisia vulgaris injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2415
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ARTEMISIA VULGARIS POLLEN (UNII: ANT994T71D) (ARTEMISIA VULGARIS POLLEN - UNII:ANT994T71D) ARTEMISIA VULGARIS POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-2415-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - WEEDS AND GARDEN PLANTS, SCALE, WING SHAD ATRIPLEX CANESCENS 
scale, wing shad atriplex canescens injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2484
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ATRIPLEX CANESCENS POLLEN (UNII: 26U0BU8G83) (ATRIPLEX CANESCENS POLLEN - UNII:26U0BU8G83) ATRIPLEX CANESCENS POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-2484-15 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - WEEDS, CARELESS/PIGWEED MIX 
careless/pigweed mix injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1302
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AMARANTHUS PALMERI POLLEN (UNII: 1GH3WV23KH) (AMARANTHUS PALMERI POLLEN - UNII:1GH3WV23KH) AMARANTHUS PALMERI POLLEN500 [PNU]  in 1 mL
AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW) (AMARANTHUS RETROFLEXUS POLLEN - UNII:73B14PX5FW) AMARANTHUS RETROFLEXUS POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-1302-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - WEEDS, DOCK/SORREL MIX 
pollens - weeds, dock/sorrel mix injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1518
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RUMEX CRISPUS POLLEN (UNII: V825XJG64G) (RUMEX CRISPUS POLLEN - UNII:V825XJG64G) RUMEX CRISPUS POLLEN500 [PNU]  in 1 mL
RUMEX ACETOSELLA POLLEN (UNII: N52MIQ81ZW) (RUMEX ACETOSELLA POLLEN - UNII:N52MIQ81ZW) RUMEX ACETOSELLA POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-1518-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - WEEDS, GIANT, SHORT, WESTERN RAGWEED MIX 
giant, short, western ragweed mix injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2319
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AMBROSIA TRIFIDA POLLEN (UNII: KU1V1898XX) (AMBROSIA TRIFIDA POLLEN - UNII:KU1V1898XX) AMBROSIA TRIFIDA POLLEN500 [PNU]  in 1 mL
AMBROSIA ARTEMISIIFOLIA POLLEN (UNII: K20Y81ACO3) (AMBROSIA ARTEMISIIFOLIA POLLEN - UNII:K20Y81ACO3) AMBROSIA ARTEMISIIFOLIA POLLEN500 [PNU]  in 1 mL
AMBROSIA PSILOSTACHYA POLLEN (UNII: RX18M46K8L) (AMBROSIA PSILOSTACHYA POLLEN - UNII:RX18M46K8L) AMBROSIA PSILOSTACHYA POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-2319-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - WEEDS, KOCHIA SCOPARIA 
kochia scoparia injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1782
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BASSIA SCOPARIA POLLEN (UNII: 07A108ZKW5) (BASSIA SCOPARIA POLLEN - UNII:07A108ZKW5) BASSIA SCOPARIA POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-1782-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - WEEDS, MARSHELDER/POVERTY MIX 
pollens - weeds, marshelder/poverty mix injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1860
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
IVA AXILLARIS POLLEN (UNII: 13KFG30UBR) (IVA AXILLARIS POLLEN - UNII:13KFG30UBR) IVA AXILLARIS POLLEN500 [PNU]  in 1 mL
IVA ANNUA POLLEN (UNII: Y2U5S5PF22) (IVA ANNUA POLLEN - UNII:Y2U5S5PF22) IVA ANNUA POLLEN500 [PNU]  in 1 mL
CYCLACHAENA XANTHIFOLIA POLLEN (UNII: V80TPZ0T6J) (CYCLACHAENA XANTHIFOLIA POLLEN - UNII:V80TPZ0T6J) CYCLACHAENA XANTHIFOLIA POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-1860-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
POLLENS - WEEDS, WEED MIX 2630 
weed mix 2630 injection, solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2631
Route of AdministrationINTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
XANTHIUM STRUMARIUM POLLEN (UNII: 2QOF601J1M) (XANTHIUM STRUMARIUM POLLEN - UNII:2QOF601J1M) XANTHIUM STRUMARIUM POLLEN500 [PNU]  in 1 mL
CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN) (CHENOPODIUM ALBUM POLLEN - UNII:098LKX5NCN) CHENOPODIUM ALBUM POLLEN500 [PNU]  in 1 mL
AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW) (AMARANTHUS RETROFLEXUS POLLEN - UNII:73B14PX5FW) AMARANTHUS RETROFLEXUS POLLEN500 [PNU]  in 1 mL
RUMEX CRISPUS POLLEN (UNII: V825XJG64G) (RUMEX CRISPUS POLLEN - UNII:V825XJG64G) RUMEX CRISPUS POLLEN500 [PNU]  in 1 mL
RUMEX ACETOSELLA POLLEN (UNII: N52MIQ81ZW) (RUMEX ACETOSELLA POLLEN - UNII:N52MIQ81ZW) RUMEX ACETOSELLA POLLEN500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65044-2631-55 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10388804/19/1941
Labeler - Jubilant HollisterStier LLC (069263643)
Registrant - Jubilant HollisterStier LLC (069263643)

Revised: 3/2018
Document Id: 28a415a2-d591-4fbe-a3e3-2559dc4b1039
Set id: d756bf9e-2e57-48a4-897a-ec1d96472dec
Version: 7
Effective Time: 20180313
 
Jubilant HollisterStier LLC