Naloxone Hydrochloride Injection
Product Images NDC 51662-1529

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 12 technical images submitted to the FDA as part of the official labeling for Naloxone Hydrochloride (NDC 51662-1529). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

51662 1529 2 Pouch Labeling

51662 1529 2 Pouch Labeling
FDA Label Image

51662 1529 3 Box Labeling

51662 1529 3 Box Labeling
FDA Label Image

51662 1529 3 Serialized Rfid Labeling

51662 1529 3 Serialized Rfid Labeling
FDA Label Image

1 (I 1)

1 (I 1)
FDA Label Image

2 (I 2)

2 (I 2)
FDA Label Image

3 (I 3)

3 (I 3)
FDA Label Image

4 (I 4)

4 (I 4)
FDA Label Image

5 (I 5)

5 (I 5)
The text appears to be a list of three terms related to different types of activation: "FINGER ACTIVATION", "THUMB ACTIVATION", and "SURFACE ACTIVATION". Without additional context, the meaning and application of these terms is not clear.*
FDA Label Image

Serialized Label (Serialized Label)

Serialized Label (Serialized Label)
FDA Label Image

Box Labeling (Single Dose Syringe Packaging)

Box Labeling (Single Dose Syringe Packaging)
Naloxone Hydrochloride Injection is a medication used as an opioid antagonist. The carton contains a single 2 mL dose disposable prefilled syringe with a 21 G x 1 ½" safety needle. It should be protected from light and stored at 25°C. The medication is for IV, IM or SC use, and the dosage is specified in the insert. The single-use syringe should not be reused or sterilized. Each mL contains 1 mg of Naloxone Hydrochloride USP and 9 mg of sodium chloride. The pH is adjusted with hydrochloric acid to meet USP limits. The package comes with the tipcap in place and should not be removed until ready to use.*
FDA Label Image

Structure (Structure)

Structure (Structure)
FDA Label Image

Syringe (Syringe Labeling)

Syringe (Syringe Labeling)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.