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Mix Of 5 Standardized Grass Pollen Injection, Solution
Product Images NDC 0268-8073
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This gallery contains 12 technical images submitted to the FDA as part of the official labeling for Mix Of 5 Standardized Grass Pollen (NDC 0268-8073). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Alk-abello, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
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What Follows Are General Guidelines For Percutaneous Testing14. Different Devices And/or Techniques Influence The Size Of The Reaction, Therefore It Is Impor¬tant To Refer To The Device Manufacturer's Or Distributor's Instructions When Grading Reac¬tions. As A Negative Control The Diluent Should Be Tested And Included In The Interpretation In The Skin Test Reactions. Use Of A Positive Control Such As Histamine Base At 1 mg/ml Should Be Used To Assess Skin Test Reactivity. (Standardized Grass Mixtures 02)
This appears to be a set of criteria for evaluating various types of skin reactions, possibly related to allergy testing or immunology research. The text describes different levels of erythema (redness and inflammation), as well as the presence or absence of wheals and pseudopods (basically, bumps or raised areas on the skin). Without more context, it's difficult to say exactly what these criteria are used for or what they mean in a broader context.*
A Negative Skin Test Is One Where The Sum Of Erythema Was 0 Or Equal To The Sum Of The Wheal. As A Negative Control, The Diluent Should Be Tested And Included In The Interpretation Of The Skin Reactions. What Follows Are General Guidelines Intradermal Testing 14. (Standardized Grass Mixtures 03)
Allergenic Extract50ml Sterile Multiple Dose Vialmidwest Mix Of Standardized Grass Pollen100,000 Bau/ml (Standardized Grass Mixtures 04)
LERGENIC EXTRAC is a standardized extract made from grass pollen. It comes in a 50mL sterile multiple dose vial with a potency of 100,000 BAU/mL. The extract is preserved with phenol 0.4% and glycerin 50% (VA) and must be stored between 2°C and 8°C. It is a prescription-only medication and the dosage is determined by a physician. The NDC number for this product is 0268:8077-50. If you need more information, please refer to the pamphlet or contact the manufacturer.*
Allergenic Extract5ml Sterile Multiple Dose Vialmixture Of 5 Standardized Grass Pollen100,000 Bau/ml (Standardized Grass Mixtures 05)
LLERGENIC EXTRA is a 5L sterile multiple dose vaccine for percutaneous testing purposes only. It is a mixture of 5 standardized grass pollens not interchangeable with grass pollen extracts. The vaccine is labeled in AU or unstandardized grass extracts. The dose is determined by a physician. The vaccine is stored between 2°C and 8°C and contains Phenol 0.4% and Glycesin 50% (vA). This product is distributed in Canada by ALK-Abello Pham. Inc. and manufactured by Port Washington, NY 11050-U.S. License 1256-sTsG1ag9sv. Complete directions are given in the accompanying circular.*
Allergenic Extract10ml Sterile Multiple Dose Vialmixture Of 7 Standardized Grass Pollen100,000 Bau/ml (Standardized Grass Mixtures 06)
This is an allergy medication called Allergenic Extra. It comes in a 10mL vial that is sterile and meant for multiple doses. The medication is a mixture of 7 different standardized grass pollen extracts that have a potency of up to 100,000 BAU/ML. It contains preservatives such as phenol and glycerin, and should be stored at a temperature between 2°C and 8°C. The label includes a GTIN number and a lot number.*
Allergenic Extractdin 023255355ml Sterile Multiple Dose Vialmixture Of Standardized Grass Mix #4-s100,000 Bau/ml (Standardized Grass Mixtures 07)
This is a description of Allergenic Extra, a sterile multiple dose vial for percutaneous testing only. It is a mixture of standardized grass MX #48 and should not be interchanged with grass pollen extracts labeled mAUhE or unstandardized grass extracts. The dose is to be determined by a physician and it must be kept between 2°C and 8°C. The prescription-only caution is listed and it should be stored with preservatives Phenol 04% and Glycerin 50%. The product is manufactured by SALIK in Port Washington, NY, and is distributed in Canada by ALK-Abello Pham. inc. in Mississauga, OnL4Z 2H6. A paragraph for ingredients is provided but not readable.*
Allergenic Extract5ml Sterile Multiple Dose Vialmixture Of 6 Standardized Grass Pollen100,000 Bau/ml (Standardized Grass Mixtures 08)
This product is a sterile multiple dose vial labeled as an allergenic extract, intended for percutaneous testing only. The mixture contains a standardized combination of 6 grass pollen seeds (non-interchangeable) and is available in either a standardized or unstandardized form. The vial is equal to 100,000 Baum. E and contains a preservative of Phenol 0.4% and Glycein 50% (v/v). The product is manufactured by Jubilant HollisterStier LLC in Port Washington, NY and has a license number of 1256 -sT6G14339v. It should be stored at a temperature between 2°C and 8°C.*
Allergenic Extract5ml Sterile Multiple Dose Vialmixture Of 7 Standardized Grass Pollen100,000 Bau/ml (Standardized Grass Mixtures 09)
This is a cautionary label for a medication that is only to be taken as prescribed by a doctor, and includes dosage information and specific product information including ingredients, storage instructions, and lot number. The medication is a mixture of seven standardized grass pollens, but cannot be interchanged with other grass pollen extracts. The label also includes a warning that the product is for percutaneous testing only.*
Allergenic Extract50ml Sterile Multiple Dose Vialmixture Of Standardized Grass Mix#4-s100,000 Bau/ml (Standardized Grass Mixtures 0a)
This text appears to be a product label for a grass extract mixture in a 50mL vial. It is standardized with grass mix #4-S and has a potency of 100,000 BAU/mL. It is stored between 2°C and 8°C and includes instructions for use. The product is licensed in the US and distributed in Canada by ALK-Abello Pharmaceuticals. No further information is available.*
Allergenic Extract10ml Sterile Multiple Dose Vialmixture Of 5 Standardized Grass Pollen100,000 Bau/ml (Standardized Grass Mixtures 0b)
This is a description of a medication called "ALLERGENIC EXTRA" in a 10 mL sterile multiple dose vial. The dose is to be determined by a physician, and cautionary statement says it is available with a prescription only. The medication is a mixture of five standardized grass pollens with a potency of 100,000 BAU/mL. It cannot be interchangeable with other grass pollen extracts unless labeled in AUML or unstandardized grass extracts. It is important to refer to the pamphlet or ingredients for further details. The medication should be stored between 2°C and 8°C, and the lot number is not available. It contains Presv., Phendl 04%, Glycerin 50% (V/V) sz. It is licensed in the United States under License 1255 - STSG22808X Sédo and is distributed in Canada by ALK-Abello Pham. Inc. in Mississauga,On.L4Z 2H6.*
Allergenic Extract10ml Sterile Multiple Dose Vialmixture Of 6 Standardized Grass Pollen100,000 Bau/ml (Standardized Grass Mixtures 0c)
This is a description of a medication. The medication is an allergenic extract used for treating allergies caused by grass pollen. The medication is available in a 10mL sterile multiple dose vial containing a mixture of 6 standardized grass pollen. The dose of the medication should be determined by a physician. The medication is only available through a prescription, and caution should be taken. It should be stored between 2°C and 8°C. The medication contains phenol 0.4% and glycerin 50% (V) as preservatives. The label has an NDC number and a GTIN number. However, the important information such as the lot number, expiration date, and name of the medication is not available.*
* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.
