Grain Mill Dust
Product Images NDC 49288-0171

3 FDA label images from Antigen Laboratories, Inc. · 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 Grain Mill Dust (NDC 49288-0171). 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.

FDA Label Image

10 mL Red Label (10mlredlabel)

10 mL Red Label (10mlredlabel)
Label for Grain Mill Dust Allergenic Extract by Antigen Laboratories, Inc. The label states the product is a 50% glycerine solution used as preservative and stabilizer. It includes a caution to refrigerate at 2 to 8 degrees Celsius and indicates a maximum initial dose of 0.02 ml per point dilution. The product is marked as non-returnable under a U.S. Government license.*
FDA Label Image

30/50 mL Red Label (30 50mlredlabel)

30/50 mL Red Label (30 50mlredlabel)
The image shows a packaging label for Grain Mill Dust allergenic extract by Antigen Laboratories, Inc. It mentions the use of 50% glycerine as a preservative and stabilizer, and includes a warning that the product is for physician use only and should be diluted prior to use. The label includes the company's P.O. Box address in Liberty, Missouri.*
FDA Label Image

5 mL Red Label (5mlredlabel)

5 mL Red Label (5mlredlabel)
Label for Grain Mill Dust allergenic extract by Antigen Laboratories, Inc. The 5 ml vial is for scratch, prick, or puncture testing. It advises refrigeration at 2°-8°C and mentions 50% glycerine as preservative and stabilizer. The product is non-returnable and regulated under U.S. Government License No. 468.*

* 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.