Adrenalin Injection
Product Images NDC 71872-7223

3 FDA label images from Medical Purchasing Solutions, Llc · 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 Adrenalin (NDC 71872-7223). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medical Purchasing Solutions, 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

71872-7223-1.pdp (71872 7223 1)

71872-7223-1.pdp (71872 7223 1)
Label for Adrenalin (epinephrine injection, USP) 1 mg/mL 1 mL single-dose vial. The label includes dosage form as injection for intravenous, intramuscular, and subcutaneous routes. It states quantity as 1 vial with placeholders for lot number and expiration date. Distributed and repackaged by Medical Purchasing Solutions, LLC in Scottsdale, AZ. The label also includes storage instructions and dilution information.*
FDA Label Image

Chemical Structure (Image 1)

Chemical Structure (Image 1)
Chemical structure of epinephrine, showing a benzene ring with three hydroxyl groups, a side chain with a hydroxyl group, and an amine group attached to the ethyl side chain, consistent with the molecular representation of epinephrine.*
FDA Label Image

1 mL Vial Label (Image 2)

1 mL Vial Label (Image 2)
Label for Adrenalin (epinephrine injection, USP) 1 mg/mL single-dose vial. The label specifies use for intravenous infusion, intramuscular, and subcutaneous routes. It notes to dilute before intravenous infusion, not for ophthalmic use, and to discard any unused portion. Distributed by Rx Pharmaceuticals in Chestnut Ridge, NY.*

* 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.