Naloxone Hydrochloride Injection, Solution
Product Images NDC 71872-7198

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 Naloxone Hydrochloride (NDC 71872-7198). 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.pdp (71872 7198 1)

71872.pdp (71872 7198 1)
Label for Naloxone Hydrochloride Injection USP 0.4 mg/mL, 1 mL single-dose vial for intravenous, intramuscular, or subcutaneous use. The label includes directions for aseptic technique, storage at 20° to 25°C, and protection from light. Manufactured for Somerset Therapeutics, LLC, repackaged and distributed by Medical Purchasing Solutions, Scottsdale, AZ.*
FDA Label Image

Molecular Structure (C768f63a 1d6f 4e4b 8f50 5b6b276029dc 01)

Molecular Structure (C768f63a 1d6f 4e4b 8f50 5b6b276029dc 01)
Chemical structure of Naloxone Hydrochloride, showing its molecular framework with functional groups and hydrochloride salt notation.*
FDA Label Image

1 mL Container Label (C768f63a 1d6f 4e4b 8f50 5b6b276029dc 02)

1 mL Container Label (C768f63a 1d6f 4e4b 8f50 5b6b276029dc 02)
Naloxone Hydrochloride Injection, USP 0.4 mg/mL label for a 1 mL single-dose vial. The label states it is for intravenous, intramuscular, or subcutaneous use and includes a warning to protect from light. Manufactured for Somerset Therapeutics, LLC, Hollywood, FL, and made in India. Includes NDC 70069-071-01 and a barcode.*

* 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.