Naloxone Hydrochloride Injection, Solution
Product Images NDC 0409-1782

5 FDA label images from Hospira, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Naloxone Hydrochloride (NDC 0409-1782). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hospira, 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

Hospira Logo (Naloxone 01)

FDA Label Image

Naloxone Formula (Naloxone 02)

Naloxone Formula (Naloxone 02)
Chemical structure of Naloxone Hydrochloride, depicting the molecular configuration including aromatic rings, hydroxyl groups, and the hydrochloride component.*
FDA Label Image

Hospira Logo (Naloxone 03)

FDA Label Image

Principal Display Panel (1 mL Cartridge Label)

Principal Display Panel (1 mL Cartridge Label)
Label for Naloxone Hydrochloride Injection, USP 0.4 mg/mL in a 1 mL single-dose Carpject sterile cartridge unit with Luer Lock. The label indicates use for intravenous, intramuscular, or subcutaneous administration. Distributed by Hospira, Inc., Lake Forest, IL. Includes dosage graduations and lot/expiration placeholders.*
FDA Label Image

Principal Display Panel (1 mL Cartridge Box)

Principal Display Panel (1 mL Cartridge Box)
Naloxone Hydrochloride Injection, USP 0.4 mg/mL packaging label for 1 mL single-dose Carpuject sterile cartridge units with Luer lock by Hospira, Inc. The label indicates use for intravenous, intramuscular, or subcutaneous injection and specifies that needles are not included. It includes storage instructions and a tamper detection package note.*

* 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.