Naloxone Hydrochloride Injection, Solution
Product Images NDC 70069-071

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 Naloxone Hydrochloride (NDC 70069-071). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Somerset Therapeutics, 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

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Chemical structure of Naloxone Hydrochloride, showing the molecular arrangement including aromatic rings, hydroxyl groups, a ketone group, and the hydrochloride salt component.*
FDA Label Image

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Label for Naloxone Hydrochloride Injection, USP 0.4 mg/mL, a 1 mL single-dose vial for intravenous, intramuscular, or subcutaneous use. The label indicates protection from light and shows the labeler as Somerset Therapeutics, LLC, Hollywood, FL. The product is made in India and includes an NDC barcode and the code number KR/DRUGS/KTK/28/289/97.*
FDA Label Image

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The label for Naloxone Hydrochloride Injection, USP 0.4 mg/mL solution shows it is manufactured by Somerset Therapeutics LLC. It is for intravenous, intramuscular, or subcutaneous use, packaged as 10 single-dose 1 mL vials. The label includes instructions for aseptic technique, storage conditions, product NDC 70069-071, 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.