Standardized Cat Pelt Injection, Solution
Product Images NDC 65044-4810

6 FDA label images from Jubilant Hollisterstier Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Standardized Cat Pelt (NDC 65044-4810). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Jubilant Hollisterstier Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Standardized Cat Pelt (Standardized Cat Pelt 1)

Standardized Cat Pelt (Standardized Cat Pelt 1)
Label for Standardized Cat Pelt allergenic extract injection solution by Jubilant HollisterStier LLC. The product has a concentration of 10,000 BAU/mL and contains inactive ingredients including 50% glycerin, 0.5% sodium chloride, and 0.275% sodium bicarbonate. The label indicates it is for percutaneous and subcutaneous use, supplied in a 5 mL container, and includes storage instructions and lot number details.*
FDA Label Image

Standardized Cat Pelt 2

Standardized Cat Pelt 2
Label for Standardized Cat Pelt allergenic extract injection solution, 10,000 BAU/mL. The product contains AP Acetone Precipitated Felis catus dander, supplied in a 5 mL quantity. It is for Rx use only, sterile, and to be stored at 2-8°C. The label notes dose and route as 1 drop topically, not interchangeable with other cat products, and contains 50% glycerin as preservative. Manufactured by Jubilant HollisterStier LLC, Spokane, WA.*
FDA Label Image

Standardized Cat Pelt 3

Standardized Cat Pelt 3
Label for Standardized Cat Pelt allergenic extract injection solution, 10,000 BAU/mL, by Jubilant HollisterStier LLC. The label includes preservative and inactive ingredients, lot and expiration information, storage instructions, and cautionary notes. The product is for percutaneous or subcutaneous use, sterile, and prescription only. NDC 65044-4810-2 is visible.*
FDA Label Image

Standardized Cat Pelt 4

Standardized Cat Pelt 4
Label for Standardized Cat Pelt allergenic extract injection, solution with a concentration of 10,000 BAU/mL in 10 mL. The label indicates acetone precipitated Felis catus dander, specifies preservative as 50% glycerin v/v, and states it is Rx only and sterile. It includes storage instructions, item and lot numbers, expiration date, and the labeler Jubilant HollisterStier LLC, Spokane, WA.*
FDA Label Image

Standardized Cat Pelt 5

Standardized Cat Pelt 5
Label for Standardized Cat Pelt injection solution, an allergenic extract containing 10,000 BAU/mL of Felis catus dander. The label includes preservative information (50% glycerin v/v), inactive ingredients, storage instructions (2-8°C), lot number, expiration date, and NDC 65044-4810-4. It is indicated for percutaneous or subcutaneous use and is sterile and non-returnable.*
FDA Label Image

Standardized Cat Pelt 6

Standardized Cat Pelt 6
Label of Standardized Cat Pelt allergenic extract injection, solution in a 50 mL container at 10,000 BAU/mL strength. It is acetone precipitated Felis catus dander for percutaneous and subcutaneous use. The label indicates it is preservative with 50% glycerin, sterile, and for prescription use only. Manufactured by Jubilant HollisterStier LLC.*

* 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.