Diphenhydramine Injection, Solution
Product Images NDC 65219-820

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Diphenhydramine (NDC 65219-820). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, 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

Diphe-img-01.jpg (Diphe Img 01)

FDA Label Image

Diphe-label-01.jpg (Diphe Label 01)

Diphe-label-01.jpg (Diphe Label 01)
Diphenhydramine Hydrochloride Injection, USP 50 mg/mL label. The product is a high potency solution for intramuscular or intravenous use, labeled as a 1 mL single dose vial. The label also includes handling instructions to protect from light and freezing, and indicates it is Rx only. The labeler is Fresenius Kabi USA, LLC.*
FDA Label Image

Diphe-label-02.jpg (Diphe Label 02)

Diphe-label-02.jpg (Diphe Label 02)
Diphenhydramine Hydrochloride Injection, USP 50 mg per mL vial label. The label states high potency with dosage form as injection for intramuscular or intravenous use. The package contains 25 single dose vials of 1 mL each. Labeler is Fresenius Kabi USA, LLC, located in Lake Zurich, IL. Storage instructions and ingredient information are also included.*
FDA Label Image

Diphe-struc-01.jpg (Diphe Struc 01)

Diphe-struc-01.jpg (Diphe Struc 01)
Chemical structure of diphenhydramine hydrochloride, showing the molecular arrangement of its components including aromatic rings and the ether and amine functional groups.*

* 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.