Diphenhydramine Hydrochloride Injection
Product Images NDC 70518-1082

3 FDA label images from Remedyrepack Inc. · 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 Diphenhydramine Hydrochloride (NDC 70518-1082). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Diphenhydramine HCl 50mg mL 70518 1082 00

Diphenhydramine HCl 50mg mL 70518 1082 00
Diphenhydramine Hydrochloride 50 mg/mL injection label. The label states it is a high potency dose for deep intramuscular or slow intravenous use, USP standard. The quantity is 1, with storage instructions and repackager information from RemedyRepack Inc. It also includes a QR code and cautions to keep medication out of reach of children.*
FDA Label Image

Diphenhydramine HCl 50mg mL 70518 1082 01

Diphenhydramine HCl 50mg mL 70518 1082 01
Label for Diphenhydramine Hydrochloride Injection USP, 50 mg/mL, high potency, supplied in quantity of 25. Intended for deep intramuscular or slow intravenous use. Label includes the NDC number 70518-1082-01, manufacturer Hikma Pharma in Amman, Jordan, and repackaging information by RemedyRepack Inc., Indiana, PA. Directions advise seeing package insert with storage conditions noted.*
FDA Label Image

Structural Formula (Diphenhydramine Hydrochloride Injection 1)

Structural Formula (Diphenhydramine Hydrochloride Injection 1)
Chemical structure of diphenhydramine hydrochloride, showing its molecular composition with aromatic rings, an ether linkage, and a dimethylamino group associated with hydrochloride.*

* 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.