Parakeet Feather
Product Images NDC 49288-0390

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Parakeet Feather (NDC 49288-0390). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Antigen Laboratories, 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.

Product Images & Figures Index

FDA Label Image

10 mL Red Label (10mlredlabel)

10 mL Red Label (10mlredlabel)
Label for Parakeet Feather Allergenic Extract by Antigen Laboratories, Inc., indicating use as an allergenic extract with preservatives. The label includes warnings and instructions for dilution and dosage, maximum initial dose recommendations, and states the product is non-returnable under U.S. Government License No. 468.*
FDA Label Image

30/50 mL Red Label (30 50mlredlabel)

30/50 mL Red Label (30 50mlredlabel)
Parakeet Feather allergenic extract by Antigen Laboratories, Inc. The label states it is for physician use only, requiring dilution prior to use, with 50% glycerine as a preservative and stabilizer. It includes a warning, storage instructions, and is marked non-returnable. The label also provides the manufacturer’s address in Liberty, MO.*
FDA Label Image

5 mL Red Label (5mlredlabel)

5 mL Red Label (5mlredlabel)
Parakeet Feather allergenic extract label by Antigen Laboratories, Inc. for scratch, prick, or puncture testing. The vial contains 5 mL and must be refrigerated at 2°-8°C. It includes 50% glycerine as a preservative and stabilizer. The label shows regulatory and return information.*

* 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.