Label: HOUSE DUST injection, solution
BLATELLA GERMANICA- german cockroach injection, solution
ACREMONIUM STRICTUM injection, solution
ALTERNARIA TENUIS- alternaria tenuis a alternata injection, solution
ASPERGILLUS FUMIGATUS injection, solution
ASPERGILLUS NIGER VAR NIGER (aspergillus niger) inje .......> FRAXINUS VELUTINA POLLEN (arizona ash) injection, solution AMARANTHUS RETROFLEXUS POLLEN (rough pigweed redroot) injection, solution LIQUIDAMBAR STYRACIFLUA POLLEN (sweetgum non stock) injection, solution JUGLANS NIGRA POLLEN (walnut black pollen) injection, solution SALIX NIGRA POLLEN- black willow injection, solution [ALK-Abello, Inc.]
FRAXINUS VELUTINA POLLEN- arizona ash injection, solution
AMARANTHUS RETROFLEXUS POLLEN- rough pigweed redroot injection, solution
LIQUIDAMBAR STYRACIFLUA POLLEN- sweetgum non stock injection, solution
JUGLANS NIGRA POLLEN- walnut black pollen injection, solution
SALIX NIGRA POLLEN- black willow injection, solution
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NDC Code(s):
0268-6000-06,
0268-6001-05,
0268-6143-06,
0268-6300-06, view more0268-6301-05, 0268-6302-06, 0268-6303-05, 0268-6304-06, 0268-6305-05, 0268-6306-06, 0268-6308-05, 0268-6309-06, 0268-6310-05, 0268-6311-06, 0268-6312-06, 0268-6314-06, 0268-6316-05, 0268-6317-06, 0268-6318-06, 0268-6319-05, 0268-6320-06, 0268-6400-06, 0268-6401-05, 0268-6402-05, 0268-6403-06, 0268-6405-06, 0268-6407-05, 0268-6500-06, 0268-6501-05, 0268-6502-06, 0268-6503-05, 0268-6504-06, 0268-6506-05, 0268-6507-06, 0268-6508-05, 0268-6509-06, 0268-6511-05, 0268-6512-06, 0268-6513-05, 0268-6514-06, 0268-6515-05, 0268-6516-06, 0268-6517-05, 0268-6518-06, 0268-6519-05, 0268-6520-06, 0268-6521-05, 0268-6524-06, 0268-6525-05, 0268-6526-06, 0268-6528-05, 0268-6529-06, 0268-6532-05, 0268-6533-06, 0268-6535-05, 0268-6536-06, 0268-6537-05, 0268-6538-06, 0268-6539-05, 0268-6540-06, 0268-6543-06, 0268-6544-05, 0268-6545-06, 0268-6547-05, 0268-6548-06, 0268-6549-05, 0268-6550-06, 0268-6552-06, 0268-6553-06, 0268-6555-05, 0268-6556-06, 0268-6557-05, 0268-6558-06, 0268-6560-05, 0268-6600-06, 0268-6601-06, 0268-6602-06, 0268-6603-06, 0268-6605-06, 0268-6606-06, 0268-6607-06, 0268-6608-06, 0268-6609-06, 0268-6610-06, 0268-6612-06, 0268-6613-06, 0268-6614-06, 0268-6615-06, 0268-6616-06, 0268-6618-06, 0268-6619-06, 0268-6620-06, 0268-6621-06, 0268-6622-06, 0268-6623-06, 0268-6625-06, 0268-6626-06, 0268-6627-06, 0268-6629-06, 0268-6630-06, 0268-6631-06, 0268-6632-06, 0268-6634-06, 0268-6635-06, 0268-6636-06, 0268-6637-06, 0268-6638-06, 0268-6639-06, 0268-6640-06, 0268-6641-06, 0268-6642-06, 0268-6643-06, 0268-6644-06, 0268-6646-06, 0268-6647-06, 0268-6648-06, 0268-6649-06, 0268-6651-06, 0268-6652-06, 0268-6654-06, 0268-6656-06, 0268-6657-06, 0268-6658-06, 0268-6659-06, 0268-6670-06, 0268-6671-06, 0268-6672-06, 0268-6674-06, 0268-6676-05, 0268-6677-06, 0268-6678-05, 0268-6679-05, 0268-6680-05, 0268-6681-06, 0268-6682-05, 0268-6683-05, 0268-6684-05, 0268-6686-05, 0268-6687-05, 0268-6688-05, 0268-6689-06, 0268-6690-05, 0268-6691-06, 0268-6692-05, 0268-6693-05, 0268-6694-05, 0268-6695-05, 0268-6696-05, 0268-6697-06, 0268-6699-05, 0268-6700-06, 0268-6701-06, 0268-6702-05, 0268-6703-05, 0268-6704-05, 0268-6705-05, 0268-6706-06, 0268-6707-05, 0268-6708-05, 0268-6709-06, 0268-6710-06, 0268-6711-05, 0268-6712-06, 0268-6713-05, 0268-6714-06, 0268-6715-05, 0268-6716-05, 0268-6717-05, 0268-6719-05, 0268-6720-05, 0268-6721-05, 0268-6722-06, 0268-6723-05, 0268-6724-05, 0268-6725-05, 0268-6726-05, 0268-6727-05, 0268-6728-06, 0268-6730-05, 0268-6731-06, 0268-6732-05, 0268-6734-05, 0268-6735-05, 0268-6736-06, 0268-6737-05, 0268-6738-05, 0268-6739-05, 0268-6740-05, 0268-6741-06, 0268-6743-06, 0268-6744-06, 0268-6745-06, 0268-6748-06, 0268-6749-06, 0268-6750-06, 0268-6751-06, 0268-6752-06, 0268-6754-06, 0268-6755-06, 0268-6757-06, 0268-6760-06, 0268-6761-06, 0268-6762-06, 0268-6763-06, 0268-6764-06, 0268-6771-06, 0268-6772-05, 0268-6773-05, 0268-6774-05, 0268-6775-05, 0268-6776-05, 0268-6777-05, 0268-6778-05, 0268-6779-05, 0268-6780-05, 0268-6781-05, 0268-6782-05, 0268-6783-05, 0268-6784-05, 0268-6785-05, 0268-6786-05, 0268-6787-05, 0268-6788-05, 0268-6790-05, 0268-6791-05, 0268-6792-05, 0268-6793-05, 0268-6794-05, 0268-6795-05, 0268-6796-05
- Packager: ALK-Abello, Inc.
- Category: NON-STANDARDIZED ALLERGENIC LABEL
- DEA Schedule: None
- Marketing Status: Biologic Licensing Application
Drug Label Information
Updated May 25, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
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BOXED WARNING
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WARNING
This product is intended for use by physicians who are experienced in the administration of allergenic extracts and the emergency care of anaphylaxis, or for use under the guidance of an allergy specialist.
As with all allergenic extracts, severe systemic reactions may occur. In certain individuals these life-threatening reactions may result in death. Fatalities associated with skin testing have been reported. Patients should be observed for at least 20 - 30 minutes following testing. Emergency measures and adequately trained personnel should be immediately available in the event of a life-threatening reaction.
Patients with unstable asthma or steroid dependent asthmatics and patients with underlying cardiovascular disease are at greater risk to a fatal outcome from a systemic allergic reaction.
Sensitive patients may experience severe anaphlactic reactions resulting in respiratory obstruction, shock, coma and/or death. Adverse events are to be reported to MedWatch (1-800-FDA-1088), Adverse Event Reporting, Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20852-9787. This product should not be injected intravenously. Patients receiving beta blockers may not be responsive to epinephrine or inhaled bronchodilators. Respiratory obstruction not responding to parenteral or inhaled bronchodilators may require theophylline, oxygen, intubation and the use of life support systems. Parenteral fluid and/or plasma expanders may be utilized for the treatment of shock. Adrenocorticosteroids may be administered parenterally or intravenously. Refer to WARNINGS, PRECAUTIONS, and ADVERSE REACTIONS sections below.
- SPL UNCLASSIFIED SECTION
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DESCRIPTION
Sterile diagnostic extracts are supplied in either phenol-saline diluent for Intradermal Testing or in diluent containing glycerin 50% (v/v) for Percutaneous Testing and phenol 0.4% (preservative). Inactive ingredients may include: sodium chloride for isotonicity, glycerin, and sodium bicarbonate as a buffer.
Pollens are individually extracted from pure pollen extracted in a phenol-preserved sodium bicarbonate solution. Short Ragweed and Mixed (Tall and Short) Ragweed extracts are standardized by Antigen E content and so labeled. The Antigen E content of extracts containing Short Ragweed at a concentration more dilute than a weight/volume ratio of 1:10 are obtained by calculating the Antigen E content based on the assay value of more concentrated extract. Pollen extracts are filtered aseptically and after final packaging, they are tested for sterility and safety. Molds are individwually extracted from pure powdered inactivated mold source material extracted in phenol preserved saline. Mold extracts are filtered aseptically and after final packaging are tested for sterility and safety.
Molds (fungi) are present in all inhabited places at all seasons of the year; they are so ubiquitous that they are prevalent at times when common allergic pollens and other inhalants are not. In the home and surroundings, molds are found in upholstered furniture, mattresses, drapes, cellar and storage room dust, woolens, leather goods, fruits, meats, cheeses, garden soil and on plants. Spores, mycelial fragments and mold residues are thus inhaled, contacted and ingested continuously.
Foods, miscellaneous inhalants and epidermals are individually extracted in phenol preserved saline or glycerin, filtered aseptically and after final packaging are tested for sterility and safety.
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CLINICAL PHARMACOLOGY
Diagnostically (for skin testing) the allergen combines with IgE antibodies fixed to mast cells in the skin. This complexing causes an increase in cellular permeability and degranulation of the mast cells releasing chemical mediators. These mediators (such as histamine) are responsible for a local inflammatory response of wheal and erythema typical of a positive skin test reaction and also, the symptoms commonly associated with allergic disease.1 The more mediator release, the larger the reaction (wheal and erythema).
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INDICATIONS AND USAGE
These products are for diagnostic use only. Diagnostic allergenic extracts are indicated for use in skin testing to establish the clinical relevance of specific allergens to which the patient has been exposed. By measuring skin test response, the physician may assess the degree of sensitivity that patients have to the allergens. For extracts standardized in AU and BAU, see individual directions for use. Allergenic extracts for diagnostic use only of coffee, mosquito, cottonseed, and flaxseed have not been shown by adequate data to be safe and effective for therapeutic use.
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CONTRAINDICATIONS
Patients on beta blockers can be non-responsive to beta agonists that may be required to reverse a systemic reaction (also, see boxed WARNING statement and ADVERSE REACTIONS). The physician should carefully weigh the benefit derived from skin testing vs. the risk to the patient should a systemic reaction arise.
Patients with unstable asthma or steroid dependent asthmatics and patients with underlying cardiovascular disease are at greater risk to a fatal outcome from a systemic allergic reaction2,3. See also PRECAUTIONS and ADVERSE REACTIONS.
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WARNINGS
Severe Allergic Reactions:
Patients should always be observed for at least 20 - 30 minutes after skin testing. In the event of a marked systemic reaction such as urticaria, angioedema, wheezing, dyspnea, respiratory obstruction, hypotension, coma and death (see ADVERSE REACTIONS), applications of a tourniquet above the injection site and administration of 0.2 mL to 1 mL (0.01 mg/kg) of epinephrine injection (1:1,000) are recommended. Maximal recommended dose for children between 2 and 12 years of age is 0.5 mL. The tourniquet is then gradually released at 15-minute intervals. Patients under treatment with beta blockers may be refractory to the usual dose of epinephrine.
Volume expanders and vasopressor agents may be required to reverse hypotension, inhalation bronchodilators and parenteral aminophylline may be required to reverse bronchospasm. In case of respiratory obstruction, oxygen and intubation may be necessary. Life-threatening reactions unresponsive to the above may require cardiopulmonary resuscitation.
Anaphylaxis Following False Negative Food Allergen Skin Test Results:
False negative skin test results associated with anaphylaxis from subsequent exposure to the allergen have been reported during postmarketing diagnostic use of some food allergenic extracts. Based on the patient’s clinical history and the index of suspicion, healthcare providers should consider confirming negative skin testing with serologic testing by measuring specific serum IgE or with a medically-supervised oral food challenge.
- PRECAUTIONS
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INFORMATION FOR PATIENTS:
Patients should be instructed to describe any active allergic symptoms such as rhinitis, wheezing, dyspnea, etc. prior to testing. Also, see ADVERSE REACTIONS and WARNINGS Sections.
Patients should always be observed 20 to 30 minutes after testing.
General:
- In the presence of active symptoms such as rhinitis, wheezing, dyspnea, etc., the indications for skin testing must be weighed carefully against the risk of temporarily aggravating the symptoms by the testing itself. Objective assessment of pulmonary function such as Peak Expiratory Flow Rate (PEFR) before allergen administration and prior to discharge may be useful in unstable asthmatics to reduce the chances of exacerbation of the patient’s asthma. Patients should be instructed to describe any active allergic symptoms as described above prior to skin testing and encouraged to report any late reactions from this testing. Also, see ADVERSE REACTIONS and WARNING sections.
- Store allergenic extracts between 2°-8°C at all times, even during use.
- Care must be taken to avoid drawing blood.
- For percutaneous testing, if blood is observed, immediately wipe the allergen from the site.
- For intradermal skin testing, pull gently on the syringe plunger and note if any blood enters the syringe. If blood is obtained, reposition the needle and repeat before injecting (see DOSAGE AND ADMINISTRATION).
- For percutaneous testing, if blood is observed, immediately wipe the allergen from the site.
- Allergenic extracts become less potent with age. Allergenic extracts containing glycerin 50% v/v are relatively stable. Non-glycerinated aqueous extracts, particularly dilute forms as used for intradermal skin testing, have been shown to be extremely unstable. Until such time as stability studies are complete with dilute allergens, new intradermal strength materials should be prepared every few weeks.
- Use standard aseptic precautions if making dilutions from stock concentrates to intradermal strength.
- For intradermal testing: Extracts in glycerin 50% v/v must be diluted with a non-glycerinated diluent and must be diluted at least 25-fold to less than 2% glycerin by volume, as glycerin above this level can cause false positive intradermal skin test results.
Pregnancy - Category C:
Animal reproduction studies have not been conducted with allergenic extracts. It is also not known whether allergenic extracts can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity.
Controlled studies of hyposensitization with moderate to high doses of allergenic extracts during conception and all trimesters of pregnancy have failed to demonstrate any risk to the fetus or to the mother4. However, on the basis of histamine’s known ability to contract the uterine muscle, the release of significant amounts of histamine from allergen exposure to skin test overdose should be avoided on theoretical grounds. Therefore, allergenic extracts should be used cautiously in a pregnant woman and only if clearly needed.
Pediatric Use:
Allergenic extracts for diagnostic use have been given safely in infants and young children. Infants have lower skin test reactivity to histamine, as well as common allergens. Skin test reactivity gradually increases to age 6 and plateaus to age 60. Therefore, small skin test reactions should be anticipated in children under age 6.
Geriatric Use:
Skin test reactivity gradually decreases after age 60. Therefore, smaller skin test reactions should be anticipated in adults over age 60.
Nursing Mothers:
It is not known if allergens administered subcutaneously appear in human milk. Because many drugs are excreted in human milk, caution should be exercised when allergenic extracts are administered to a nursing woman.
Drug Interactions:
Drugs can interfere with the performance of skin tests5.
Antihistamines: Response to mediator (histamine) released by allergens is suppressed by antihistamines. The length of suppression varies and is dependent on individual patient, type of antihistamine and length of time the patient has been on antihistamines. The duration of this suppression may be as little as 24 hours (chlorpheniramine) and can be as long as 40 days (astemizole).
Tricyclic Antidepressants: These exert a potent and sustained decrease of skin reactivity to histamine which may last for a few weeks.
Beta2 Agonists: Oral terbutaline and parenteral ephedrine, in general, have been shown to decrease allergen induced wheal.
Dopamine: Intravenous infusion of dopamine may inhibit skin test responses.
Beta Blocking Agents: Propranolol can significantly increase skin test reactivity.
Other Drugs: Short acting steroids, inhaled beta2 agonists, theophylline and cromolyn do not seem to affect skin test response.
- In the presence of active symptoms such as rhinitis, wheezing, dyspnea, etc., the indications for skin testing must be weighed carefully against the risk of temporarily aggravating the symptoms by the testing itself. Objective assessment of pulmonary function such as Peak Expiratory Flow Rate (PEFR) before allergen administration and prior to discharge may be useful in unstable asthmatics to reduce the chances of exacerbation of the patient’s asthma. Patients should be instructed to describe any active allergic symptoms as described above prior to skin testing and encouraged to report any late reactions from this testing. Also, see ADVERSE REACTIONS and WARNING sections.
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ADVERSE REACTIONS
Fatalities from skin testing in the United States have been extensively reviewed by Lockey.2 Six fatalities were associated with intradermal testing without previous percutaneous testing, and one was associated with a combination of percutaneous (scratch) and intradermal skin testing. With careful attention to dosage and administration, fatal reactions occur infrequently, but it must be remembered that allergenic extracts are highly potent to sensitive individuals and overdosage could result in anaphylactic symptoms. Therefore, it is imperative that physicians administering allergenic extracts for skin testing understand, and be prepared for the treatment of severe reactions.
Local:
Immediate wheal and erythema reactions are to be expected; but if very large, may be the first manifestation of a systemic reaction. In such cases, immediately wipe the test site(s) with sterile gauze or cotton to remove excess allergen.
Systemic Reactions:
Systemic reactions are characterized by one or more of the following symptoms: sneezing, mild to severe generalized urticaria, itching (other than at the skin test site), extensive or generalized edema, wheezing, asthma, dyspnea, cyanosis, hypotension, syncope, and upper airway obstruction. Symptoms may progress to shock and death. Patients should always be observed for at least 20 - 30 minutes after testing.
Volume expanders and vasopressor agents may be required to reverse hypotension. Inhalational bronchodilators and parenteral aminophylline may be required to reverse bronchospasm. Severe airway obstruction unresponsive to bronchodilator may require tracheal intubation and use of oxygen. In the event of a marked systemic reaction, application of a tourniquet above the injection site and the administration of 0.2 mL to 1.0 mL of epinephrine injection (1:1,000) is recommended. Maximum recommended dose for children between 2 and 12 years of age is 0.3 mL. The tourniquet should not be left in place without loosening for 90 seconds every 15 minutes.
Adverse events should be reported via MedWatch (1-800-FDA-1088), Adverse Event Reporting, Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20852-9787.
- OVERDOSAGE
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DOSAGE AND ADMINISTRATION
Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.
Skin test techniques for immediate (Type I) hypersensitivity testing fall into two major categories: percutaneous, and intracutaneous.
Percutaneous techniques:
For percutaneous testing, in general, skin is scratched, punctured or pricked just before the allergen is applied or through a drop of test allergen. There are several devices available for this technique. Refer to the manufacturer or distributor’s circular for specific directions for their use.
In General:
- It is recommended that the test areas should be placed no closer than 4 - 5 cm apart to avoid interference of reactions when several tests are applied.
- Skin test areas should be cleansed with alcohol and air dried.
- Preferably, the allergen should be placed on the volar surface of the forearm, upper arm, or the patient’s back. The patient should be placed in a comfortable position prior to testing.
- For scratch testing, a sharp, clean, sterile instrument is used to abrade the skin, but not to draw blood. Each scratch should be about 2 - 4 mm in length. A small drop of extract is placed on the surface of the skin.
- Prick testing: For prick testing, a sharp, sterile instrument is used to puncture the skin slightly, applying it at a 15 - 20° angle to the skin. The instrument is gently raised, “tenting” the skin until it pops out, generally pricking through the drop of allergen. Do not draw blood.
- For puncture testing, a sharp, clean, sterile instrument must be used. Puncture the skin, through the drop of allergen, perpendicular to the skin. Do not draw blood.
For all of the above techniques, a separate instrument must be used for each patient; if the instrument is to be used to pass through the allergen, to avoid cross-contamination, a separate instrument is to be used for each allergen. The test should be read in 15 minutes, measuring both wheal size and erythema.
Intracutaneous (intradermal) testing:
General: Intradermal testing is more sensitive than percutaneous testing and its specificity is dependent on dose. Intradermal testing is not intended as an initial screen unless used in highly dilute solutions. Intradermal testing is usually reserved for allergens that have demonstrated either negative or equivocal percutaneous skin test response in the face of positive or unclear history.
Intradermal testing of one allergen in several serial dilutions (beginning with the weakest to the more concentrated dilutions) may also be useful in assessing degree of patient sensitivity for the establishment of a safe starting dose for immunotherapy.
Bulk extracts must be diluted for intradermal testing. Use of Sterile Diluent for Allergenic Extracts or Sterile Diluent for Allergenic Extracts Normal Saline with HSA (albumin saline) is recommended. Dilutions should be made with sterile disposable syringes using aseptic technique. Commonly 10 fold dilutions are used to achieve a desired concentration for intradermal testing and continuation of immunotherapy. For example, transferring 0.5 mL of a 10,000 PNU/mL extract into 4.5 mL of diluent will yield 5 mL of extract at 1,000 PNU/mL. For weight volume products, a 1:100 w/v dilution may be prepared from a 1:10 w/v by transferring 0.5 mL of the 1:10 w/v to 4.5 mL of diluent. Prepare as many additional serial dilutions as necessary to reach the appropriate concentration. As a general rule intradermal strength should begin at no higher than 1/100 to 1/1000 of the percutaneous strength that resulted in a negative skin test reaction.
- It is recommended that the test areas should be spaced no less than 5 cm apart to avoid interference with adjacent allergen or control.
- Skin should be cleansed with alcohol and air dried.
- A sterile 1 mL or 1/2 mL syringe with a 26 - 30 gauge needle should be used. A separate sterile syringe should be used for each extract and each patient.
- Care should be taken to eliminate air bubbles from the syringe prior to injecting the test dose. It is suggested that not more than 6 - 10 allergens of each different type be used at any one time. Very sensitive patients may show rapid response.
- The skin is held tensely, and the needle is inserted almost parallel to the skin, beveled side up far enough to cover the beveled portion. Slowly inject sufficient extract to make a small bleb of approximately 5 mm in diameter (0.01 - 0.02 mL).
- Read the test results in 15 minutes.
Selection of the proper strength for intracutaneous testing: A general rule for the prevention of untoward reactions, particularly in extremely sensitive patients, is to screen by percutaneous methods initially, and begin intradermal testing at a strength not more than 1/100 of a negative or equivocal percutaneous reaction.
Controls:
In both percutaneous and intracutaneous tests, a negative control test with diluent alone should be performed because some patients exhibit dermographia, and/or other non-specific irritant responses.
As a positive control in the evaluation of allergenic skin testing, histamine 1 mg/mL (histamine base) should be used for percutaneous testing, and histamine 0.1 mg/mL (histamine base) should be used for intradermal testing.
Interpretation of results:
Patient’s response is graded on the basis of the size of erythema or wheal.6 General guidelines follow for percutaneous testing, different devices and/or techniques influence the size of the reaction, therefore it is important to refer to the device manufacturer’s or distributor’s instructions when grading reactions.
Percutaneous (prick or scratch) test:
0 No reaction or less than control.
+ Erythema greater than control, smaller than a nickel (21 mm diameter).
++ Erythema greater than a nickel in diameter, no wheal.
+++ Wheal and erythema without pseudopods.
++++ Wheal and erythema with pseudopods.
Intradermal test:
0 No reaction or less than negative control.
+ 3-4 mm wheal with erythema, or erythema alone larger than a nickel (21 mm diameter).
++ 4-8 mm wheal and erythema, without pseudopods.
+++ Over 8 mm wheal and erythema without pseudopods.
++++ Wheal and erythema with pseudopods.
- It is recommended that the test areas should be placed no closer than 4 - 5 cm apart to avoid interference of reactions when several tests are applied.
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HOW SUPPLIED
For scratch and prick testing: 5 mL dropper applicator vials in 50% v/v glycerin or 10mL stoppered vial in 50% v/v glycerin. Available individually and in a complete set of the most common allergens. Available in either Protein Nitrogen Units (PNU/mL) or weight to volume (w/v).
For intracutaneous testing: 5 mL sterile vials, aqueous based, individually and in a complete set of the most common allergens. Available in either Protein Nitrogen Units (PNU/mL) or weight to volume (w/v).
Histatrol® Positive skin test control - histamine. 1 mg/mL and 0.1 mg/mL histamine base.
See Product Catalog for specific diagnostic concentrations available.
- STORAGE
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REFERENCES
- Holgate, S.T., Robinson, C. and Church, M.K. Mediators of immediate hypersensitivity. In Middleton et al: Allergy Principles and Practice, St. Louis, 1988, C.V. Mosby, p 135.
- Lockey, R.F., et al. Fatalities from immunotherapy (IT) and skin testing (ST). J. Allergy Clin. Immunol. 1987: 79: 660.
- Reid, M.J. et al. Survey of fatalities from skin testing and immunotherapy. 1985-1989. J. Allergy Clin Immunol. 1993; 92:6.
- DeBuske L. M. et al. Special problems regarding Allergen Immunotherapy in Immunology and Allergy Clinics of North America, Greenburger, P.A. Ed. February 1992; 145-149.
- Bousquet, J. In vivo methods for the study of allergy: skin test, techniques and interpretation. In: Middleton et al.: Allergy Principles and Practice 3rd Ed. St. Louis: CV Mosby, 1988:167.
- Freedman, S.O. Asthma and Allergic Rhinitis II. Clinical Aspects, in Freedman and Gold Clinical Immunology 2nd Ed. New York: Harper & Row, 1976: 131.
Revised February 2023 No. 112S
© ALK-Abelló, Inc.
Distributed in Canada by:
ALK-Abelló Pharmaceuticals, Inc.
#35-151 Brunel Road
Mississauga, Ontario
Canada L4Z 2H6 - Holgate, S.T., Robinson, C. and Church, M.K. Mediators of immediate hypersensitivity. In Middleton et al: Allergy Principles and Practice, St. Louis, 1988, C.V. Mosby, p 135.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HOUSE DUST
house dust injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6000 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOUSE DUST (UNII: EYO007VX98) (HOUSE DUST - UNII:EYO007VX98) HOUSE DUST 10000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6000-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 06/30/2013 BLATELLA GERMANICA
german cockroach injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6405 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BLATTELLA GERMANICA (UNII: G9O67I0A8Q) (BLATTELLA GERMANICA - UNII:G9O67I0A8Q) BLATTELLA GERMANICA 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6405-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 ACREMONIUM STRICTUM
acremonium strictum injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6500 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SAROCLADIUM STRICTUM (UNII: 3F36V0451W) (SAROCLADIUM STRICTUM - UNII:3F36V0451W) SAROCLADIUM STRICTUM 0.10 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6500-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 ALTERNARIA TENUIS
alternaria tenuis a alternata injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6502 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA 0.10 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6502-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 ASPERGILLUS FUMIGATUS
aspergillus fumigatus injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6504 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS 0.10 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6504-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 ASPERGILLUS NIGER VAR NIGER
aspergillus niger injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6507 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER 0.10 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6507-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 AUREOBASIDIUM PULLULANS VAR PULLULANS
pullularia pullulans injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6509 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS 0.10 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6509-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 BOTRYTIS CINEREA
botrytis cinerea injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6512 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7) BOTRYTIS CINEREA 0.10 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6512-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 CANDIDA ALBICANS
candida albicans injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6514 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS 0.10 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6514-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 CHAETOMIUM GLOBOSUM
chaetomium globosum injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6516 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A) CHAETOMIUM GLOBOSUM 0.10 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6516-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 CLADOSPORIUM CLADOSPORIOIDES
cladosporium cladosporioides hormodendrum clad injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6518 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CLADOSPORIUM CLADOSPORIOIDES (UNII: 4ZWY20GTGO) (CLADOSPORIUM CLADOSPORIOIDES - UNII:4ZWY20GTGO) CLADOSPORIUM CLADOSPORIOIDES 0.10 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6518-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 CLADOSPORIUM SPHAEROSPERMUM
cladosporium sphaerospermum hormodendrum hordei injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6520 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM 0.10 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6520-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 COCHLIOBOLUS SATIVUS
helminthosporium sorokinianum injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6524 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS 0.10 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6524-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 EPICOCCUM NIGRUM
epicoccum nigrum injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6526 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM 0.10 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6526-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 FUSARIUM OXYSPORUM VASINFECTUM
fusarium spp injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6529 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FUSARIUM OXYSPORUM VASINFECTUM (UNII: 6M98DC08TZ) (FUSARIUM OXYSPORUM VASINFECTUM - UNII:6M98DC08TZ) FUSARIUM OXYSPORUM VASINFECTUM 0.10 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6529-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 HELMINTHOSPORIUM SOLANI
helminthosporium solani spondylocladium injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6533 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HELMINTHOSPORIUM SOLANI (UNII: U6Z259H815) (HELMINTHOSPORIUM SOLANI - UNII:U6Z259H815) HELMINTHOSPORIUM SOLANI 0.10 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6533-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 11/30/2021 MUCOR PLUMBEUS
mucor spp injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6536 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS 0.10 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6536-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 NEUROSPORA INTERMEDIA
neurospora spp injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6538 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI) NEUROSPORA INTERMEDIA 0.10 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6538-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 11/30/2021 KHUSKIA ORYZAE
nigrospora spp injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6540 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength KHUSKIA ORYZAE (UNII: VK8C112WTS) (KHUSKIA ORYZAE - UNII:VK8C112WTS) KHUSKIA ORYZAE 0.10 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6540-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 11/30/2021 PHOMA EXIGUA VAR EXIGUA
phoma herbarum injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6543 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PHOMA EXIGUA VAR. EXIGUA (UNII: 8JAG41IE4M) (PHOMA EXIGUA VAR. EXIGUA - UNII:8JAG41IE4M) PHOMA EXIGUA VAR. EXIGUA 0.10 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6543-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 RHIZOPUS ARRHIZUS VAR ARRHIZUS
rhizopus spp injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6545 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RHIZOPUS ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS - UNII:8476849N1Y) RHIZOPUS ARRHIZUS 0.10 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6545-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 RHODOTORULA RUBRA
rhodotorula rubra injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6548 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RHODOTORULA RUBRA (UNII: 15W81V867R) (RHODOTORULA RUBRA - UNII:15W81V867R) RHODOTORULA RUBRA 0.10 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6548-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 USTILAGO MAYDIS
corn smut injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6550 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength USTILAGO MAYDIS (UNII: 4K7Z7K7SWG) (USTILAGO MAYDIS - UNII:4K7Z7K7SWG) USTILAGO MAYDIS 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6550-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 11/30/2021 USTILAGO TRITICI
wheat smut injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6552 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength USTILAGO TRITICI (UNII: BV82OL2IZ8) (USTILAGO TRITICI - UNII:BV82OL2IZ8) USTILAGO TRITICI 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6552-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 STEMPHYLIUM SOLANI
stemphylium spp injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6553 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength STEMPHYLIUM SOLANI (UNII: 1IEK4UDP5M) (STEMPHYLIUM SOLANI - UNII:1IEK4UDP5M) STEMPHYLIUM SOLANI 0.10 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6553-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 TRICHOPHYTON MENTAGROPHYTES
trichophyton mentagrophytes injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6556 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV) TRICHOPHYTON MENTAGROPHYTES 0.10 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6556-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 KARAYA GUM
karaya gum bassora injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6143 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength KARAYA GUM (UNII: 73W9IQY50Q) (KARAYA GUM - UNII:73W9IQY50Q) KARAYA GUM 0.005 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6143-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 BOS TAURUS SKIN
cattle epithelium injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6300 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BOS TAURUS SKIN (UNII: 7J12CD6O9L) (BOS TAURUS SKIN - UNII:7J12CD6O9L) BOS TAURUS SKIN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6300-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 COTTON FIBER
cattle epithelium injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6302 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength COTTON FIBER (UNII: 70LDW53ROO) (COTTON FIBER - UNII:70LDW53ROO) COTTON FIBER 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6302-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 COTTON SEED
cottonseed injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6304 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength COTTON SEED (UNII: DI0ZRJ0MXN) (COTTON SEED - UNII:DI0ZRJ0MXN) COTTON SEED 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6304-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 CANIS LUPUS FAMILIARIS SKIN
dog epithelium injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6306 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CANIS LUPUS FAMILIARIS SKIN (UNII: X2W7CLE97T) (CANIS LUPUS FAMILIARIS SKIN - UNII:X2W7CLE97T) CANIS LUPUS FAMILIARIS SKIN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6306-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 CAVIA PORCELLUS SKIN
guinea pig epithelium injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6309 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAVIA PORCELLUS SKIN (UNII: GM3H4U6QS8) (CAVIA PORCELLUS SKIN - UNII:GM3H4U6QS8) CAVIA PORCELLUS SKIN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6309-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 EQUUS CABALLUS SKIN
horse epithelium injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6311 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EQUUS CABALLUS SKIN (UNII: 88VZV9HGT4) (EQUUS CABALLUS SKIN - UNII:88VZV9HGT4) EQUUS CABALLUS SKIN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6311-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 CEIBA PENTANDRA FIBER
kapok injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6312 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CEIBA PENTANDRA FIBER (UNII: 758Z9H9WV9) (CEIBA PENTANDRA FIBER - UNII:758Z9H9WV9) CEIBA PENTANDRA FIBER 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6312-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 MUS MUSCULUS SKIN
mouse epithelium injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6314 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MUS MUSCULUS SKIN (UNII: 390AN9GB09) (MUS MUSCULUS SKIN - UNII:390AN9GB09) MUS MUSCULUS SKIN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6314-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 ORRIS
iris x germanica root injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6317 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IRIS X GERMANICA ROOT (UNII: 8N6VTJ9IWV) (IRIS X GERMANICA ROOT - UNII:8N6VTJ9IWV) IRIS X GERMANICA ROOT 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6317-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 PYRETHRUM CINERARIIFOLIUM
pyrethrum injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6318 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TANACETUM CINERARIIFOLIUM FLOWER (UNII: CGF76TP7X6) (TANACETUM CINERARIIFOLIUM FLOWER - UNII:CGF76TP7X6) TANACETUM CINERARIIFOLIUM FLOWER 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6318-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 11/30/2021 RABBIT
rabbit epithelium injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6320 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RABBIT (UNII: O5V0F26RUW) (RABBIT - UNII:O5V0F26RUW) RABBIT 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6320-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 SOLENOPSIS INVICTA
fire ant injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6400 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SOLENOPSIS INVICTA (UNII: 5O7CR4P444) (SOLENOPSIS INVICTA - UNII:5O7CR4P444) SOLENOPSIS INVICTA 0.01 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6400-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 PERIPLANETA AMERICANA
american cockroach injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6403 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (PERIPLANETA AMERICANA - UNII:2RQ1L9N089) PERIPLANETA AMERICANA 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6403-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 PENICILLIUM CHRYSOGENUM VAR CHRYSOGENUM
yeast saccharomyces cerevisiae injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6558 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 0.10 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6558-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 ACACIA
acacia injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6600 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACACIA (UNII: 5C5403N26O) (ACACIA - UNII:5C5403N26O) ACACIA 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6600-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 ALNUS INCANA SSP RUGOSA POLLEN
white alder injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6601 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALNUS INCANA SUBSP. RUGOSA POLLEN (UNII: 605T96G8Y5) (ALNUS INCANA SUBSP. RUGOSA POLLEN - UNII:605T96G8Y5) ALNUS INCANA SUBSP. RUGOSA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6601-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 MEDICAGO SATIVA POLLEN
alfalfa injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6602 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MEDICAGO SATIVA POLLEN (UNII: G515RAI9FY) (MEDICAGO SATIVA POLLEN - UNII:G515RAI9FY) MEDICAGO SATIVA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6602-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 FRAXINUS AMERICANA POLLEN
white ash injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6603 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q) (FRAXINUS AMERICANA POLLEN - UNII:G684LX721Q) FRAXINUS AMERICANA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6603-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 PASPALUM NOTATUM POLLEN
bahia grass injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6605 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK) (PASPALUM NOTATUM POLLEN - UNII:V003SHB7VK) PASPALUM NOTATUM POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6605-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 MORELLA CERIFERA POLLEN
bayberry wax myrtle injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6606 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MORELLA CERIFERA POLLEN (UNII: LC8MEV9S89) (MORELLA CERIFERA POLLEN - UNII:LC8MEV9S89) MORELLA CERIFERA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6606-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 FAGUS GRANDIFOLIA POLLEN
beech injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6607 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FAGUS GRANDIFOLIA POLLEN (UNII: 34X886W1H4) (FAGUS GRANDIFOLIA POLLEN - UNII:34X886W1H4) FAGUS GRANDIFOLIA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6607-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 BETULA LENTA POLLEN
black birch injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6608 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BETULA LENTA POLLEN (UNII: JQ5HI5004M) (BETULA LENTA POLLEN - UNII:JQ5HI5004M) BETULA LENTA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6608-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 BETULA NIGRA POLLEN
river birch red injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6609 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BETULA NIGRA POLLEN (UNII: 93963RFO1P) (BETULA NIGRA POLLEN - UNII:93963RFO1P) BETULA NIGRA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6609-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 BETULA LENTA POLLEN
white birch injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6610 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BETULA LENTA POLLEN (UNII: JQ5HI5004M) (BETULA LENTA POLLEN - UNII:JQ5HI5004M) BETULA LENTA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6610-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 ACER NEGUNDO POLLEN
box elder ash leaf maple injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6612 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACER NEGUNDO POLLEN (UNII: P6K070AR8V) (ACER NEGUNDO POLLEN - UNII:P6K070AR8V) ACER NEGUNDO POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6612-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 AMARANTHUS PALMERI POLLEN
carelessweed injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6613 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMARANTHUS PALMERI POLLEN (UNII: 1GH3WV23KH) (AMARANTHUS PALMERI POLLEN - UNII:1GH3WV23KH) AMARANTHUS PALMERI POLLEN 0.025 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6613-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 JUNIPERUS ASHEI POLLEN
mountain cedar injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6614 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength JUNIPERUS ASHEI POLLEN (UNII: 544F8MEY0Y) (JUNIPERUS ASHEI POLLEN - UNII:544F8MEY0Y) JUNIPERUS ASHEI POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6614-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 JUNIPERUS VIRGINIANA POLLEN
red cedar injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6615 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength JUNIPERUS VIRGINIANA POLLEN (UNII: PY0JA16R2G) (JUNIPERUS VIRGINIANA POLLEN - UNII:PY0JA16R2G) JUNIPERUS VIRGINIANA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6615-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 XANTHIUM STRUMARIUM VAR CANADENSE POLLEN
cocklebur injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6616 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN (UNII: 0ZK6G3W3BI) (XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN - UNII:0ZK6G3W3BI) XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6616-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 POPULUS DELTOIDES POLLEN
eastern cottonwood common injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6618 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POPULUS DELTOIDES POLLEN (UNII: 476DVV63WP) (POPULUS DELTOIDES POLLEN - UNII:476DVV63WP) POPULUS DELTOIDES POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6618-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 CUPRESSUS ARIZONICA POLLEN
arizona cypress injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6619 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CUPRESSUS ARIZONICA POLLEN (UNII: 232DMH0XVF) (CUPRESSUS ARIZONICA POLLEN - UNII:232DMH0XVF) CUPRESSUS ARIZONICA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6619-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 TAXODIUM DISTICHUM POLLEN
bald cypress injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6620 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TAXODIUM DISTICHUM POLLEN (UNII: O12H03B41R) (TAXODIUM DISTICHUM POLLEN - UNII:O12H03B41R) TAXODIUM DISTICHUM POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6620-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 RUMEX ACETOSELLA POLLEN
sour dock sheep sorrel injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6621 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RUMEX ACETOSELLA POLLEN (UNII: N52MIQ81ZW) (RUMEX ACETOSELLA POLLEN - UNII:N52MIQ81ZW) RUMEX ACETOSELLA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6621-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 RUMEX CRISPUS POLLEN
yellow dock injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6622 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RUMEX CRISPUS POLLEN (UNII: V825XJG64G) (RUMEX CRISPUS POLLEN - UNII:V825XJG64G) RUMEX CRISPUS POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6622-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 ULMUS AMERICANA POLLEN
american elm injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6623 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ULMUS AMERICANA POLLEN (UNII: 89BAT511BD) (ULMUS AMERICANA POLLEN - UNII:89BAT511BD) ULMUS AMERICANA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6623-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 SOLIDAGO CANADENSIS POLLEN
goldenrod injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6625 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SOLIDAGO CANADENSIS POLLEN (UNII: 644CZ16IR5) (SOLIDAGO CANADENSIS POLLEN - UNII:644CZ16IR5) SOLIDAGO CANADENSIS POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6625-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 CELTIS OCCIDENTALIS POLLEN
hackberry injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6626 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CELTIS OCCIDENTALIS POLLEN (UNII: 68R9X9Y96X) (CELTIS OCCIDENTALIS POLLEN - UNII:68R9X9Y96X) CELTIS OCCIDENTALIS POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6626-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 CARYA OVATA POLLEN
shagbark hickory injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6627 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CARYA OVATA POLLEN (UNII: 54UN9R2798) (CARYA OVATA POLLEN - UNII:54UN9R2798) CARYA OVATA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6627-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 SORGHUM HALEPENSE POLLEN
johnson grass injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6629 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP) (SORGHUM HALEPENSE POLLEN - UNII:577VA5B4HP) SORGHUM HALEPENSE POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6629-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 JUNIPERUS CALIFORNICA POLLEN
western juniper injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6630 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength JUNIPERUS CALIFORNICA POLLEN (UNII: 0H1V4V5V9L) (JUNIPERUS CALIFORNICA POLLEN - UNII:0H1V4V5V9L) JUNIPERUS CALIFORNICA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6630-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 KOCHIA SCOPARIA POLLEN
kochia firebush injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6631 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BASSIA SCOPARIA POLLEN (UNII: 07A108ZKW5) (BASSIA SCOPARIA POLLEN - UNII:07A108ZKW5) BASSIA SCOPARIA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6631-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 CHENOPODIUM ALBUM POLLEN
lambs quarters injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6632 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN) (CHENOPODIUM ALBUM POLLEN - UNII:098LKX5NCN) CHENOPODIUM ALBUM POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6632-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 ACER RUBRUM POLLEN
red maple injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6634 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACER RUBRUM POLLEN (UNII: 700NK45C76) (ACER RUBRUM POLLEN - UNII:700NK45C76) ACER RUBRUM POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6634-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 ACER SACCHARUM POLLEN
sugar maple injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6635 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACER SACCHARUM POLLEN (UNII: V38QUQ7861) (ACER SACCHARUM POLLEN - UNII:V38QUQ7861) ACER SACCHARUM POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6635-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 IVA XANTHIFOLIA POLLEN
burweed marshelder injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6636 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CYCLACHAENA XANTHIFOLIA POLLEN (UNII: V80TPZ0T6J) (CYCLACHAENA XANTHIFOLIA POLLEN - UNII:V80TPZ0T6J) CYCLACHAENA XANTHIFOLIA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6636-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 IVA ANNUA VAR ANNUA POLLEN
rough marshelder injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6637 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IVA ANNUA POLLEN (UNII: Y2U5S5PF22) (IVA ANNUA POLLEN - UNII:Y2U5S5PF22) IVA ANNUA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6637-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 PROSOPIS JULIFLORA POLLEN
mesquite injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6638 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PROSOPIS JULIFLORA POLLEN (UNII: 6EIJ3D04MR) (PROSOPIS JULIFLORA POLLEN - UNII:6EIJ3D04MR) PROSOPIS JULIFLORA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6638-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 ARTEMISIA VULGARIS POLLEN
common mugwort injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6639 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARTEMISIA VULGARIS POLLEN (UNII: ANT994T71D) (ARTEMISIA VULGARIS POLLEN - UNII:ANT994T71D) ARTEMISIA VULGARIS POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6639-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 MORUS RUBRA POLLEN
red mulberry injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6640 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MORUS RUBRA POLLEN (UNII: 9LYI4RTZ52) (MORUS RUBRA POLLEN - UNII:9LYI4RTZ52) MORUS RUBRA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6640-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 MORUS ALBA POLLEN
white mulberry injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6641 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MORUS ALBA POLLEN (UNII: 3I9T68187H) (MORUS ALBA POLLEN - UNII:3I9T68187H) MORUS ALBA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6641-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 QUERCUS RUBRA POLLEN
red oak injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6642 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength QUERCUS RUBRA POLLEN (UNII: SVW19ET93C) (QUERCUS RUBRA POLLEN - UNII:SVW19ET93C) QUERCUS RUBRA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6642-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 QUERCUS VIRGINIANA POLLEN
virginia live oak injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6643 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength QUERCUS VIRGINIANA POLLEN (UNII: 8KDG09A4GO) (QUERCUS VIRGINIANA POLLEN - UNII:8KDG09A4GO) QUERCUS VIRGINIANA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6643-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 QUERCUS ALBA POLLEN
white oak injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6644 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK) (QUERCUS ALBA POLLEN - UNII:Z4Y9ZSV4KK) QUERCUS ALBA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6644-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 OLEA EUROPAEA POLLEN
olive pollen injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6646 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OLEA EUROPAEA POLLEN (UNII: 43R41XZ627) (OLEA EUROPAEA POLLEN - UNII:43R41XZ627) OLEA EUROPAEA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6646-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 SYAGRUS ROMANZOFFIANA POLLEN
queen palm coco palm injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6647 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SYAGRUS ROMANZOFFIANA POLLEN (UNII: 84ZOM591BB) (SYAGRUS ROMANZOFFIANA POLLEN - UNII:84ZOM591BB) SYAGRUS ROMANZOFFIANA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6647-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 CARYA ILLINOINENSIS POLLEN
pecan pollen injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6648 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CARYA ILLINOINENSIS POLLEN (UNII: PYO4JR720Y) (CARYA ILLINOINENSIS POLLEN - UNII:PYO4JR720Y) CARYA ILLINOINENSIS POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6648-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 AMARANTHUS RETROFLEXUS POLLEN
rough pigweed injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6649 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW) (AMARANTHUS RETROFLEXUS POLLEN - UNII:73B14PX5FW) AMARANTHUS RETROFLEXUS POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6649-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 PINUS STROBUS POLLEN
white pine injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6651 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PINUS STROBUS POLLEN (UNII: TX1ER5UV3T) (PINUS STROBUS POLLEN - UNII:TX1ER5UV3T) PINUS STROBUS POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6651-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 PLANTAGO LANCEOLATA POLLEN
english plantain injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6652 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI) (PLANTAGO LANCEOLATA POLLEN - UNII:DO87T1U2CI) PLANTAGO LANCEOLATA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6652-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 POPULUS ALBA POLLEN
white poplar injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6654 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POPULUS ALBA POLLEN (UNII: VU8C8SB23P) (POPULUS ALBA POLLEN - UNII:VU8C8SB23P) POPULUS ALBA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6654-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 LIGUSTRUM VULGARE POLLEN
privet injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6656 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIGUSTRUM VULGARE POLLEN (UNII: Y3FRX92Z0E) (LIGUSTRUM VULGARE POLLEN - UNII:Y3FRX92Z0E) LIGUSTRUM VULGARE POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6656-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 ELYMUS REPENS POLLEN
quack grass injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6657 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ELYMUS REPENS POLLEN (UNII: ON2T85TA2O) (ELYMUS REPENS POLLEN - UNII:ON2T85TA2O) ELYMUS REPENS POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6657-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 AMBROSIA TRIFIDA POLLEN
tall ragweed giant injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6658 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMBROSIA TRIFIDA POLLEN (UNII: KU1V1898XX) (AMBROSIA TRIFIDA POLLEN - UNII:KU1V1898XX) AMBROSIA TRIFIDA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6658-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 SALSOLA KALI POLLEN
russian thistle injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6659 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALSOLA KALI POLLEN (UNII: 2MH135KC6G) (SALSOLA KALI POLLEN - UNII:2MH135KC6G) SALSOLA KALI POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6659-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 ARTEMISIA TRIDENTATA POLLEN
common sagebrush injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6670 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARTEMISIA TRIDENTATA POLLEN (UNII: YI19RB8YFD) (ARTEMISIA TRIDENTATA POLLEN - UNII:YI19RB8YFD) ARTEMISIA TRIDENTATA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6670-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 LIQUIDAMBAR STYRACIFLUA POLLEN
sweetgum injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6671 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIQUIDAMBAR STYRACIFLUA POLLEN (UNII: 5Q246DS5BS) (LIQUIDAMBAR STYRACIFLUA POLLEN - UNII:5Q246DS5BS) LIQUIDAMBAR STYRACIFLUA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6671-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 PLATANUS OCCIDENTALIS POLLEN
american sycamore injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6672 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PLATANUS OCCIDENTALIS POLLEN (UNII: E03U1K03LK) (PLATANUS OCCIDENTALIS POLLEN - UNII:E03U1K03LK) PLATANUS OCCIDENTALIS POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6672-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 JUGLANS NIGRA POLLEN
black pollen walnut injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6674 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (JUGLANS NIGRA POLLEN - UNII:1BV28146ZR) JUGLANS NIGRA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6674-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 AILANTHUS ALTISSIMA POLLEN
ailanthus tree of heaven injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6677 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AILANTHUS ALTISSIMA POLLEN (UNII: 2A64U81OQ3) (AILANTHUS ALTISSIMA POLLEN - UNII:2A64U81OQ3) AILANTHUS ALTISSIMA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6677-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 11/30/2021 POPULUS TREMULOIDES POLLEN
aspen injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6681 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POPULUS TREMULOIDES POLLEN (UNII: 928OC2TJDA) (POPULUS TREMULOIDES POLLEN - UNII:928OC2TJDA) POPULUS TREMULOIDES POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6681-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 11/30/2021 POA ANNUA POLLEN
annual bluegrass injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6689 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POA ANNUA POLLEN (UNII: 7U437HHU5C) (POA ANNUA POLLEN - UNII:7U437HHU5C) POA ANNUA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6689-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 BROMUS INERMIS POLLEN
brome grass injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6691 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BROMUS INERMIS POLLEN (UNII: 766QT72BK6) (BROMUS INERMIS POLLEN - UNII:766QT72BK6) BROMUS INERMIS POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6691-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 ZEA MAYS POLLEN
corn pollen injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6697 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZEA MAYS POLLEN (UNII: 74PD8J616H) (ZEA MAYS POLLEN - UNII:74PD8J616H) ZEA MAYS POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6697-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 POPULUS FREMONTII POLLEN
fremont cottonwood injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6700 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POPULUS FREMONTII POLLEN (UNII: 426RHB4302) (POPULUS FREMONTII POLLEN - UNII:426RHB4302) POPULUS FREMONTII POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6700-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 11/30/2021 POPULUS DELTOIDES SSP MONILIFERA POLLEN
western cottonwood injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6701 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN (UNII: 5928LJ1441) (POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN - UNII:5928LJ1441) POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6701-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 EUPATORIUM CAPILLIFOLIUM POLLEN
dog fennel injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6706 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EUPATORIUM CAPILLIFOLIUM POLLEN (UNII: B67NF86HF0) (EUPATORIUM CAPILLIFOLIUM POLLEN - UNII:B67NF86HF0) EUPATORIUM CAPILLIFOLIUM POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6706-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 ULMUS CRASSIFOLIA POLLEN
cedar elm injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6709 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ULMUS CRASSIFOLIA POLLEN (UNII: G82398SD3I) (ULMUS CRASSIFOLIA POLLEN - UNII:G82398SD3I) ULMUS CRASSIFOLIA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6709-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 ULMUS PUMILA POLLEN
chinese elm injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6710 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ULMUS PUMILA POLLEN (UNII: 030R993R8E) (ULMUS PUMILA POLLEN - UNII:030R993R8E) ULMUS PUMILA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6710-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 EUCALYPTUS GLOBULUS POLLEN
eucalyptus injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6712 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EUCALYPTUS GLOBULUS POLLEN (UNII: 7XW7TB10X9) (EUCALYPTUS GLOBULUS POLLEN - UNII:7XW7TB10X9) EUCALYPTUS GLOBULUS POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6712-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 CORYLUS AMERICANA POLLEN
hazelnut pollen injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6714 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CORYLUS AMERICANA POLLEN (UNII: ZGS382Y3AV) (CORYLUS AMERICANA POLLEN - UNII:ZGS382Y3AV) CORYLUS AMERICANA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6714-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 11/30/2021 ROBINIA PSEUDOACACIA POLLEN
black locust injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6722 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ROBINIA PSEUDOACACIA POLLEN (UNII: 8003NOJ82F) (ROBINIA PSEUDOACACIA POLLEN - UNII:8003NOJ82F) ROBINIA PSEUDOACACIA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6722-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 11/30/2021 MELALEUCA QUINQUENERVIA POLLEN
melaleuca pollen injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6728 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MELALEUCA QUINQUENERVIA POLLEN (UNII: NX974IRT8E) (MELALEUCA QUINQUENERVIA POLLEN - UNII:NX974IRT8E) MELALEUCA QUINQUENERVIA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6728-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 CHENOPODIUM AMBROSIOIDES POLLEN
mexican tea injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6731 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHENOPODIUM AMBROSIOIDES POLLEN (UNII: WIB701MW2H) (CHENOPODIUM AMBROSIOIDES POLLEN - UNII:WIB701MW2H) CHENOPODIUM AMBROSIOIDES POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6731-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 06/30/2013 QUERCUS AGRIFOLIA POLLEN
california live oak coast injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6736 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength QUERCUS AGRIFOLIA POLLEN (UNII: VOT5MA71M7) (QUERCUS AGRIFOLIA POLLEN - UNII:VOT5MA71M7) QUERCUS AGRIFOLIA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6736-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 11/30/2021 QUERCUS ALBA POLLEN
wild pollen oat injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6741 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK) (QUERCUS ALBA POLLEN - UNII:Z4Y9ZSV4KK) QUERCUS ALBA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6741-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 11/30/2021 SCHINUS MOLLE POLLEN
california pepper tree injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6743 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SCHINUS MOLLE POLLEN (UNII: M0G28FH9K1) (SCHINUS MOLLE POLLEN - UNII:M0G28FH9K1) SCHINUS MOLLE POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6743-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 AMARANTHUS SPINOSUS POLLEN
spiny pigweed injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6744 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMARANTHUS SPINOSUS POLLEN (UNII: 380W4HYR6N) (AMARANTHUS SPINOSUS POLLEN - UNII:380W4HYR6N) AMARANTHUS SPINOSUS POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6744-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 CASUARINA EQUISETIFOLIA POLLEN
australian pine beefwood injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6745 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CASUARINA EQUISETIFOLIA POLLEN (UNII: OZJ4OE173N) (CASUARINA EQUISETIFOLIA POLLEN - UNII:OZJ4OE173N) CASUARINA EQUISETIFOLIA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6745-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 PINUS ECHINATA POLLEN
yellow pine injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6748 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PINUS ECHINATA POLLEN (UNII: 96LRW14765) (PINUS ECHINATA POLLEN - UNII:96LRW14765) PINUS ECHINATA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6748-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 AMBROSIA ACANTHICARPA POLLEN
false ragweed bur injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6749 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMBROSIA ACANTHICARPA POLLEN (UNII: U2AI3H2J5Y) (AMBROSIA ACANTHICARPA POLLEN - UNII:U2AI3H2J5Y) AMBROSIA ACANTHICARPA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6749-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 AMBROSIA TENUIFOLIA POLLEN
slender ragweed injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6750 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMBROSIA TENUIFOLIA POLLEN (UNII: 57W5SO585B) (AMBROSIA TENUIFOLIA POLLEN - UNII:57W5SO585B) AMBROSIA TENUIFOLIA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6750-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 AMBROSIA BIDENTATA POLLEN
southern ragweed injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6751 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMBROSIA BIDENTATA POLLEN (UNII: M3S672G75O) (AMBROSIA BIDENTATA POLLEN - UNII:M3S672G75O) AMBROSIA BIDENTATA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6751-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 11/30/2021 AMBROSIA PSILOSTACHYA POLLEN
western ragweed injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6752 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMBROSIA PSILOSTACHYA POLLEN (UNII: RX18M46K8L) (AMBROSIA PSILOSTACHYA POLLEN - UNII:RX18M46K8L) AMBROSIA PSILOSTACHYA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6752-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 LOLIUM PERENNE SSP MULTIFLORUM POLLEN
italian rye grass injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6754 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LOLIUM MULTIFLORUM POLLEN (UNII: VJI0WKK736) (LOLIUM MULTIFLORUM POLLEN - UNII:VJI0WKK736) LOLIUM MULTIFLORUM POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6754-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 11/30/2021 ARTEMISIA FRIGIDA POLLEN
prairie sage injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6755 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARTEMISIA FRIGIDA POLLEN (UNII: 5AN5LR8L3F) (ARTEMISIA FRIGIDA POLLEN - UNII:5AN5LR8L3F) ARTEMISIA FRIGIDA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6755-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 11/30/2021 DISTICHLIS SPICATA POLLEN
salt grass injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6757 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DISTICHLIS SPICATA POLLEN (UNII: GOA51670YV) (DISTICHLIS SPICATA POLLEN - UNII:GOA51670YV) DISTICHLIS SPICATA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6757-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 HOLCUS LANATUS POLLEN
velvet grass injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6760 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOLCUS LANATUS POLLEN (UNII: 70O1TP6H01) (HOLCUS LANATUS POLLEN - UNII:70O1TP6H01) HOLCUS LANATUS POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6760-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 JUGLANS NIGRA POLLEN
california walnut black pollen injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6761 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (JUGLANS NIGRA POLLEN - UNII:1BV28146ZR) JUGLANS NIGRA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6761-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 JUGLANS REGIA POLLEN
english walnut pollen injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6762 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength JUGLANS REGIA POLLEN (UNII: ARW43087I1) (JUGLANS REGIA POLLEN - UNII:ARW43087I1) JUGLANS REGIA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6762-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 11/30/2021 TRITICUM AESTIVUM POLLEN
wheat pollen injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6763 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRITICUM AESTIVUM POLLEN (UNII: F1KAH8374D) (TRITICUM AESTIVUM POLLEN - UNII:F1KAH8374D) TRITICUM AESTIVUM POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6763-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 11/30/2021 ARTEMISIA ANNUA POLLEN
common wormwood annual injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6764 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARTEMISIA ANNUA POLLEN (UNII: 36R82U4DL6) (ARTEMISIA ANNUA POLLEN - UNII:36R82U4DL6) ARTEMISIA ANNUA POLLEN 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6764-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 AMARANTHUS TUBERCULATUS POLLEN
water hemp injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6771 Route of Administration PERCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMARANTHUS TUBERCULATUS POLLEN (UNII: 92N6W6KO2G) (AMARANTHUS TUBERCULATUS POLLEN - UNII:92N6W6KO2G) AMARANTHUS TUBERCULATUS POLLEN 0.025 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 1 mL PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6771-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 HOUSE DUST
house dust injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6001 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOUSE DUST (UNII: EYO007VX98) (HOUSE DUST - UNII:EYO007VX98) HOUSE DUST 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6001-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 06/30/2013 BOS TAURUS SKIN
cattle epithelium injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6301 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BOS TAURUS SKIN (UNII: 7J12CD6O9L) (BOS TAURUS SKIN - UNII:7J12CD6O9L) BOS TAURUS SKIN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6301-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 COTTON FIBER
cotton linters injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6303 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength COTTON FIBER (UNII: 70LDW53ROO) (COTTON FIBER - UNII:70LDW53ROO) COTTON FIBER 0.001 g in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6303-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 CANIS LUPUS FAMILIARIS SKIN
dog epithelium injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6305 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CANIS LUPUS FAMILIARIS SKIN (UNII: X2W7CLE97T) (CANIS LUPUS FAMILIARIS SKIN - UNII:X2W7CLE97T) CANIS LUPUS FAMILIARIS SKIN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6305-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 CAVIA PORCELLUS SKIN
guinea pig epithelium injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6308 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAVIA PORCELLUS SKIN (UNII: GM3H4U6QS8) (CAVIA PORCELLUS SKIN - UNII:GM3H4U6QS8) CAVIA PORCELLUS SKIN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6308-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 EQUUS CABALLUS SKIN
horse epithelium injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6310 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EQUUS CABALLUS SKIN (UNII: 88VZV9HGT4) (EQUUS CABALLUS SKIN - UNII:88VZV9HGT4) EQUUS CABALLUS SKIN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6310-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 11/30/2021 MUS MUSCULUS SKIN
mouse epithelium injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6316 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MUS MUSCULUS SKIN (UNII: 390AN9GB09) (MUS MUSCULUS SKIN - UNII:390AN9GB09) MUS MUSCULUS SKIN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6316-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 RABBIT
rabbit epithelium injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6319 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RABBIT (UNII: O5V0F26RUW) (RABBIT - UNII:O5V0F26RUW) RABBIT 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6319-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 SOLENOPSIS INVICTA
fire ant injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6401 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SOLENOPSIS INVICTA (UNII: 5O7CR4P444) (SOLENOPSIS INVICTA - UNII:5O7CR4P444) SOLENOPSIS INVICTA 10 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6401-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 PERIPLANETA AMERICANA
american cockroach injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6402 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (PERIPLANETA AMERICANA - UNII:2RQ1L9N089) PERIPLANETA AMERICANA 100 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6402-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 11/30/2021 BLATELLA GERMANICA
german cockroach injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6407 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BLATTELLA GERMANICA (UNII: G9O67I0A8Q) (BLATTELLA GERMANICA - UNII:G9O67I0A8Q) BLATTELLA GERMANICA 100 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6407-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 ACREMONIUM STRICTUM
acremonium cephalosporium injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6501 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACREMONIUM STRICTUM (UNII: 3F36V0451W) (ACREMONIUM STRICTUM - UNII:3F36V0451W) ACREMONIUM STRICTUM 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6501-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 ALTERNARIA TENUIS
alternaria tenuis a alternata injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6503 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6503-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 ASPERGILLUS FUMIGATUS
aspergillus fumigatus injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6506 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6506-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 ASPERGILLUS NIGER VAR NIGER
aspergillus niger injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6508 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6508-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 AUREOBASIDIUM PULLULANS VAR PULLULANS
aureobasidium pullularia pullulans injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6511 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6511-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 BOTRYTIS CINEREA
botrytis cinerea injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6513 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7) BOTRYTIS CINEREA 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6513-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 CANDIDA ALBICANS
candida albicans injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6515 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6515-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 CHAETOMIUM GLOBOSUM
chaetomium globosum injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6517 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A) CHAETOMIUM GLOBOSUM 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6517-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 CLADOSPORIUM CLADOSPORIOIDES
cladosporium cladosporioides hormodendrum clad injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6519 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CLADOSPORIUM CLADOSPORIOIDES (UNII: 4ZWY20GTGO) (CLADOSPORIUM CLADOSPORIOIDES - UNII:4ZWY20GTGO) CLADOSPORIUM CLADOSPORIOIDES 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6519-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 CLADOSPORIUM SPHAEROSPERMUM
cladosporium sphaerospermum hormodendrum hordei injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6521 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6521-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 COCHLIOBOLUS SATIVUS
drechslera helminthosporium injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6525 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6525-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 EPICOCCUM NIGRUM
epicoccum nigrum injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6528 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6528-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 FUSARIUM OXYSPORUM VASINFECTUM
fusarium spp injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6532 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FUSARIUM OXYSPORUM VASINFECTUM (UNII: 6M98DC08TZ) (FUSARIUM OXYSPORUM VASINFECTUM - UNII:6M98DC08TZ) FUSARIUM OXYSPORUM VASINFECTUM 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6532-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 HELMINTHOSPORIUM SOLANI
helminthosporium solani spondylocladium injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6535 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HELMINTHOSPORIUM SOLANI (UNII: U6Z259H815) (HELMINTHOSPORIUM SOLANI - UNII:U6Z259H815) HELMINTHOSPORIUM SOLANI 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6535-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 MUCOR PLUMBEUS
helminthmucor spp injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6537 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6537-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 NEUROSPORA INTERMEDIA
neurospora spp injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6539 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI) NEUROSPORA INTERMEDIA 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6539-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 PHOMA EXIGUA VAR EXIGUA
phoma herbarum injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6544 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PHOMA EXIGUA VAR. EXIGUA (UNII: 8JAG41IE4M) (PHOMA EXIGUA VAR. EXIGUA - UNII:8JAG41IE4M) PHOMA EXIGUA VAR. EXIGUA 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6544-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 RHIZOPUS ARRHIZUS VAR ARRHIZUS
rhizopus spp injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6547 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RHIZOPUS ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS - UNII:8476849N1Y) RHIZOPUS ARRHIZUS 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6547-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 RHODOTORULA RUBRA
rhodotorula rubra injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6549 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RHODOTORULA RUBRA (UNII: 15W81V867R) (RHODOTORULA RUBRA - UNII:15W81V867R) RHODOTORULA RUBRA 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6549-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 STEMPHYLIUM SOLANI
stemphylium spp injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6555 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength STEMPHYLIUM SOLANI (UNII: 1IEK4UDP5M) (STEMPHYLIUM SOLANI - UNII:1IEK4UDP5M) STEMPHYLIUM SOLANI 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6555-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 TRICHOPHYTON MENTAGROPHYTES
trichophyton mentagrophytes injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6557 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV) TRICHOPHYTON MENTAGROPHYTES 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6557-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 SACCHAROMYCES CEREVISIAE
yeast saccharomyces cerevisiae injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6560 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) (SACCHAROMYCES CEREVISIAE - UNII:978D8U419H) SACCHAROMYCES CEREVISIAE 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6560-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 ACACIA
acacia injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6676 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACACIA (UNII: 5C5403N26O) (ACACIA - UNII:5C5403N26O) ACACIA 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6676-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 ALNUS INCANA SSP RUGOSA POLLEN
white alder injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6678 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALNUS INCANA SUBSP. RUGOSA POLLEN (UNII: 605T96G8Y5) (ALNUS INCANA SUBSP. RUGOSA POLLEN - UNII:605T96G8Y5) ALNUS INCANA SUBSP. RUGOSA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6678-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 FRAXINUS VELUTINA POLLEN
arizona ash injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6679 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FRAXINUS VELUTINA POLLEN (UNII: LJT6I6Z8FD) (FRAXINUS VELUTINA POLLEN - UNII:LJT6I6Z8FD) FRAXINUS VELUTINA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6679-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 FRAXINUS AMERICANA POLLEN
white ash injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6680 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q) (FRAXINUS AMERICANA POLLEN - UNII:G684LX721Q) FRAXINUS AMERICANA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6680-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 PASPALUM NOTATUM POLLEN
bahia grass injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6682 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK) (PASPALUM NOTATUM POLLEN - UNII:V003SHB7VK) PASPALUM NOTATUM POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6682-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 MORELLA CERIFERA POLLEN
bayberry wax myrtle injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6683 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MORELLA CERIFERA POLLEN (UNII: LC8MEV9S89) (MORELLA CERIFERA POLLEN - UNII:LC8MEV9S89) MORELLA CERIFERA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6683-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 FAGUS GRANDIFOLIA POLLEN
beech injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6684 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FAGUS GRANDIFOLIA POLLEN (UNII: 34X886W1H4) (FAGUS GRANDIFOLIA POLLEN - UNII:34X886W1H4) FAGUS GRANDIFOLIA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6684-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 BETULA LENTA POLLEN
black birch injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6686 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BETULA LENTA POLLEN (UNII: JQ5HI5004M) (BETULA LENTA POLLEN - UNII:JQ5HI5004M) BETULA LENTA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6686-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 BETULA NIGRA POLLEN
river birch red injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6687 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BETULA NIGRA POLLEN (UNII: 93963RFO1P) (BETULA NIGRA POLLEN - UNII:93963RFO1P) BETULA NIGRA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6687-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 BETULA LENTA POLLEN
white birch injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6688 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BETULA LENTA POLLEN (UNII: JQ5HI5004M) (BETULA LENTA POLLEN - UNII:JQ5HI5004M) BETULA LENTA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6688-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 ACER NEGUNDO POLLEN
box elder ash leaf maple injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6690 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACER NEGUNDO POLLEN (UNII: P6K070AR8V) (ACER NEGUNDO POLLEN - UNII:P6K070AR8V) ACER NEGUNDO POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6690-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 BROMUS INERMIS POLLEN
brome grass injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6692 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BROMUS INERMIS POLLEN (UNII: 766QT72BK6) (BROMUS INERMIS POLLEN - UNII:766QT72BK6) BROMUS INERMIS POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6692-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 AMARANTHUS PALMERI POLLEN
carelessweed injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6693 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMARANTHUS PALMERI POLLEN (UNII: 1GH3WV23KH) (AMARANTHUS PALMERI POLLEN - UNII:1GH3WV23KH) AMARANTHUS PALMERI POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6693-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 JUNIPERUS ASHEI POLLEN
mountain cedar injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6694 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength JUNIPERUS ASHEI POLLEN (UNII: 544F8MEY0Y) (JUNIPERUS ASHEI POLLEN - UNII:544F8MEY0Y) JUNIPERUS ASHEI POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6694-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 JUNIPERUS VIRGINIANA POLLEN
red cedar injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6695 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength JUNIPERUS VIRGINIANA POLLEN (UNII: PY0JA16R2G) (JUNIPERUS VIRGINIANA POLLEN - UNII:PY0JA16R2G) JUNIPERUS VIRGINIANA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6695-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 XANTHIUM STRUMARIUM VAR CANADENSE POLLEN
cocklebur injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6696 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN (UNII: 0ZK6G3W3BI) (XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN - UNII:0ZK6G3W3BI) XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6696-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 POPULUS DELTOIDES POLLEN
eastern cottonwood common injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6699 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POPULUS DELTOIDES POLLEN (UNII: 476DVV63WP) (POPULUS DELTOIDES POLLEN - UNII:476DVV63WP) POPULUS DELTOIDES POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6699-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 POPULUS DELTOIDES SSP MONILIFERA POLLEN
western cottonwood injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6702 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN (UNII: 5928LJ1441) (POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN - UNII:5928LJ1441) POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6702-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 CUPRESSUS ARIZONICA POLLEN
arizona cypress injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6703 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CUPRESSUS ARIZONICA POLLEN (UNII: 232DMH0XVF) (CUPRESSUS ARIZONICA POLLEN - UNII:232DMH0XVF) CUPRESSUS ARIZONICA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6703-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 RUMEX ACETOSELLA POLLEN
sour dock sheep sorrel injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6704 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RUMEX ACETOSELLA POLLEN (UNII: N52MIQ81ZW) (RUMEX ACETOSELLA POLLEN - UNII:N52MIQ81ZW) RUMEX ACETOSELLA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6704-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 RUMEX CRISPUS POLLEN
yellow dock injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6705 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RUMEX CRISPUS POLLEN (UNII: V825XJG64G) (RUMEX CRISPUS POLLEN - UNII:V825XJG64G) RUMEX CRISPUS POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6705-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 EUPATORIUM CAPILLIFOLIUM POLLEN
dog fennel injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6707 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EUPATORIUM CAPILLIFOLIUM POLLEN (UNII: B67NF86HF0) (EUPATORIUM CAPILLIFOLIUM POLLEN - UNII:B67NF86HF0) EUPATORIUM CAPILLIFOLIUM POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6707-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 ULMUS AMERICANA POLLEN
american elm injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6708 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ULMUS AMERICANA POLLEN (UNII: 89BAT511BD) (ULMUS AMERICANA POLLEN - UNII:89BAT511BD) ULMUS AMERICANA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6708-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 11/30/2021 ULMUS PUMILA POLLEN
chinese elm injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6711 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ULMUS PUMILA POLLEN (UNII: 030R993R8E) (ULMUS PUMILA POLLEN - UNII:030R993R8E) ULMUS PUMILA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6711-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 EUCALYPTUS GLOBULUS POLLEN
eucalyptus injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6713 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EUCALYPTUS GLOBULUS POLLEN (UNII: 7XW7TB10X9) (EUCALYPTUS GLOBULUS POLLEN - UNII:7XW7TB10X9) EUCALYPTUS GLOBULUS POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6713-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 CORYLUS AMERICANA POLLEN
hazelnut pollen injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6715 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CORYLUS AMERICANA POLLEN (UNII: ZGS382Y3AV) (CORYLUS AMERICANA POLLEN - UNII:ZGS382Y3AV) CORYLUS AMERICANA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6715-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 CARYA OVATA POLLEN
shagbark hickory injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6716 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CARYA OVATA POLLEN (UNII: 54UN9R2798) (CARYA OVATA POLLEN - UNII:54UN9R2798) CARYA OVATA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6716-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 SORGHUM HALEPENSE POLLEN
johnson grass injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6717 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP) (SORGHUM HALEPENSE POLLEN - UNII:577VA5B4HP) SORGHUM HALEPENSE POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6717-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 JUNIPERUS CALIFORNICA POLLEN
western juniper injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6719 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength JUNIPERUS CALIFORNICA POLLEN (UNII: 0H1V4V5V9L) (JUNIPERUS CALIFORNICA POLLEN - UNII:0H1V4V5V9L) JUNIPERUS CALIFORNICA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6719-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 KOCHIA SCOPARIA POLLEN
kochia firebush injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6720 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BASSIA SCOPARIA POLLEN (UNII: 07A108ZKW5) (BASSIA SCOPARIA POLLEN - UNII:07A108ZKW5) BASSIA SCOPARIA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6720-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 CHENOPODIUM ALBUM POLLEN
lambs quarters injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6721 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN) (CHENOPODIUM ALBUM POLLEN - UNII:098LKX5NCN) CHENOPODIUM ALBUM POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6721-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 ROBINIA PSEUDOACACIA POLLEN
black locust injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6723 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ROBINIA PSEUDOACACIA POLLEN (UNII: 8003NOJ82F) (ROBINIA PSEUDOACACIA POLLEN - UNII:8003NOJ82F) ROBINIA PSEUDOACACIA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6723-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 ACER RUBRUM POLLEN
red maple injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6724 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACER RUBRUM POLLEN (UNII: 700NK45C76) (ACER RUBRUM POLLEN - UNII:700NK45C76) ACER RUBRUM POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6724-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 ACER SACCHARUM POLLEN
sugar maple injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6725 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACER SACCHARUM POLLEN (UNII: V38QUQ7861) (ACER SACCHARUM POLLEN - UNII:V38QUQ7861) ACER SACCHARUM POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6725-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 IVA XANTHIFOLIA POLLEN
burweed marshelder injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6726 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CYCLACHAENA XANTHIFOLIA POLLEN (UNII: V80TPZ0T6J) (CYCLACHAENA XANTHIFOLIA POLLEN - UNII:V80TPZ0T6J) CYCLACHAENA XANTHIFOLIA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6726-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 IVA ANNUA VAR ANNUA POLLEN
rough marshelder injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6727 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IVA ANNUA POLLEN (UNII: Y2U5S5PF22) (IVA ANNUA POLLEN - UNII:Y2U5S5PF22) IVA ANNUA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6727-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 PROSOPIS JULIFLORA POLLEN
mesquite injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6730 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PROSOPIS JULIFLORA POLLEN (UNII: 6EIJ3D04MR) (PROSOPIS JULIFLORA POLLEN - UNII:6EIJ3D04MR) PROSOPIS JULIFLORA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6730-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 ARTEMISIA VULGARIS POLLEN
common mugwort injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6732 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARTEMISIA VULGARIS POLLEN (UNII: ANT994T71D) (ARTEMISIA VULGARIS POLLEN - UNII:ANT994T71D) ARTEMISIA VULGARIS POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6732-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 MORUS RUBRA POLLEN
red mulberry injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6734 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MORUS RUBRA POLLEN (UNII: 9LYI4RTZ52) (MORUS RUBRA POLLEN - UNII:9LYI4RTZ52) MORUS RUBRA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6734-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 MORUS ALBA POLLEN
white mulberry injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6735 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MORUS ALBA POLLEN (UNII: 3I9T68187H) (MORUS ALBA POLLEN - UNII:3I9T68187H) MORUS ALBA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6735-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 QUERCUS AGRIFOLIA POLLEN
california live oak coast injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6737 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength QUERCUS AGRIFOLIA POLLEN (UNII: VOT5MA71M7) (QUERCUS AGRIFOLIA POLLEN - UNII:VOT5MA71M7) QUERCUS AGRIFOLIA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6737-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 QUERCUS RUBRA POLLEN
red oak injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6738 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength QUERCUS RUBRA POLLEN (UNII: SVW19ET93C) (QUERCUS RUBRA POLLEN - UNII:SVW19ET93C) QUERCUS RUBRA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6738-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 QUERCUS VIRGINIANA POLLEN
virginia live oak injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6739 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength QUERCUS VIRGINIANA POLLEN (UNII: 8KDG09A4GO) (QUERCUS VIRGINIANA POLLEN - UNII:8KDG09A4GO) QUERCUS VIRGINIANA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6739-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 QUERCUS ALBA POLLEN
white oak injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6740 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK) (QUERCUS ALBA POLLEN - UNII:Z4Y9ZSV4KK) QUERCUS ALBA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6740-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 BETULA LENTA POLLEN
white pine injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6772 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BETULA LENTA POLLEN (UNII: JQ5HI5004M) (BETULA LENTA POLLEN - UNII:JQ5HI5004M) BETULA LENTA POLLEN 0.002 g in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6772-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 OLEA EUROPAEA POLLEN
olive pollen injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6773 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OLEA EUROPAEA POLLEN (UNII: 43R41XZ627) (OLEA EUROPAEA POLLEN - UNII:43R41XZ627) OLEA EUROPAEA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6773-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 SYAGRUS ROMANZOFFIANA POLLEN
queen palm coco palm injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6774 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SYAGRUS ROMANZOFFIANA POLLEN (UNII: 84ZOM591BB) (SYAGRUS ROMANZOFFIANA POLLEN - UNII:84ZOM591BB) SYAGRUS ROMANZOFFIANA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6774-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 CARYA ILLINOINENSIS POLLEN
pecan pollen injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6775 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CARYA ILLINOINENSIS POLLEN (UNII: PYO4JR720Y) (CARYA ILLINOINENSIS POLLEN - UNII:PYO4JR720Y) CARYA ILLINOINENSIS POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6775-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 AMARANTHUS RETROFLEXUS POLLEN
rough pigweed redroot injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6776 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW) (AMARANTHUS RETROFLEXUS POLLEN - UNII:73B14PX5FW) AMARANTHUS RETROFLEXUS POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6776-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 CASUARINA EQUISETIFOLIA POLLEN
australian pine beefwood injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6777 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CASUARINA EQUISETIFOLIA POLLEN (UNII: OZJ4OE173N) (CASUARINA EQUISETIFOLIA POLLEN - UNII:OZJ4OE173N) CASUARINA EQUISETIFOLIA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6777-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 PLANTAGO LANCEOLATA POLLEN
english plantain injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6778 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI) (PLANTAGO LANCEOLATA POLLEN - UNII:DO87T1U2CI) PLANTAGO LANCEOLATA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6778-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 POPULUS ALBA POLLEN
white poplar injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6779 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POPULUS ALBA POLLEN (UNII: VU8C8SB23P) (POPULUS ALBA POLLEN - UNII:VU8C8SB23P) POPULUS ALBA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6779-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 LIGUSTRUM VULGARE POLLEN
privet injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6780 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIGUSTRUM VULGARE POLLEN (UNII: Y3FRX92Z0E) (LIGUSTRUM VULGARE POLLEN - UNII:Y3FRX92Z0E) LIGUSTRUM VULGARE POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6780-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 AMBROSIA ACANTHICARPA POLLEN
false ragweed bur injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6781 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMBROSIA ACANTHICARPA POLLEN (UNII: U2AI3H2J5Y) (AMBROSIA ACANTHICARPA POLLEN - UNII:U2AI3H2J5Y) AMBROSIA ACANTHICARPA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6781-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 AMBROSIA TRIFIDA POLLEN
tall ragweed giant injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6782 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMBROSIA TRIFIDA POLLEN (UNII: KU1V1898XX) (AMBROSIA TRIFIDA POLLEN - UNII:KU1V1898XX) AMBROSIA TRIFIDA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6782-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 AMBROSIA PSILOSTACHYA POLLEN
western ragweed injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6783 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMBROSIA PSILOSTACHYA POLLEN (UNII: RX18M46K8L) (AMBROSIA PSILOSTACHYA POLLEN - UNII:RX18M46K8L) AMBROSIA PSILOSTACHYA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6783-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 SALSOLA KALI POLLEN
russian thistle injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6784 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALSOLA KALI POLLEN (UNII: 2MH135KC6G) (SALSOLA KALI POLLEN - UNII:2MH135KC6G) SALSOLA KALI POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6784-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 ARTEMISIA FRIGIDA POLLEN
prairie sage injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6785 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARTEMISIA FRIGIDA POLLEN (UNII: 5AN5LR8L3F) (ARTEMISIA FRIGIDA POLLEN - UNII:5AN5LR8L3F) ARTEMISIA FRIGIDA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6785-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 ARTEMISIA TRIDENTATA POLLEN
common sagebrush injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6786 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARTEMISIA TRIDENTATA POLLEN (UNII: YI19RB8YFD) (ARTEMISIA TRIDENTATA POLLEN - UNII:YI19RB8YFD) ARTEMISIA TRIDENTATA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6786-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 LIQUIDAMBAR STYRACIFLUA POLLEN
sweetgum non stock injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6787 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIQUIDAMBAR STYRACIFLUA POLLEN (UNII: 5Q246DS5BS) (LIQUIDAMBAR STYRACIFLUA POLLEN - UNII:5Q246DS5BS) LIQUIDAMBAR STYRACIFLUA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6787-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 PLATANUS OCCIDENTALIS POLLEN
american sycamore injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6788 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PLATANUS OCCIDENTALIS POLLEN (UNII: E03U1K03LK) (PLATANUS OCCIDENTALIS POLLEN - UNII:E03U1K03LK) PLATANUS OCCIDENTALIS POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6788-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 HOLCUS LANATUS POLLEN
velvet grass injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6790 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOLCUS LANATUS POLLEN (UNII: 70O1TP6H01) (HOLCUS LANATUS POLLEN - UNII:70O1TP6H01) HOLCUS LANATUS POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6790-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 JUGLANS NIGRA POLLEN
walnut black pollen injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6791 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (JUGLANS NIGRA POLLEN - UNII:1BV28146ZR) JUGLANS NIGRA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6791-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 JUGLANS NIGRA POLLEN
california walnut black pollen injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6792 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (JUGLANS NIGRA POLLEN - UNII:1BV28146ZR) JUGLANS NIGRA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6792-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 JUGLANS REGIA POLLEN
english walnut pollen injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6793 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength JUGLANS REGIA POLLEN (UNII: ARW43087I1) (JUGLANS REGIA POLLEN - UNII:ARW43087I1) JUGLANS REGIA POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0268-6793-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA103753 01/01/1965 05/22/2023 AMARANTHUS TUBERCULATUS POLLEN
water hemp injection, solutionProduct Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6794 Route of Administration INTRADERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMARANTHUS TUBERCULATUS POLLEN (UNII: 92N6W6KO2G) (AMARANTHUS TUBERCULATUS POLLEN - UNII:92N6W6KO2G) AMARANTHUS TUBERCULATUS POLLEN 1000 [PNU] in 1 mL Inactive Ingredients Ingredient Name Strength PHENOL (UNII: 339NCG44TV) 0.004 mL in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g in 1 mL SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE