Diphenhydramine Hydrochloride Injection
Product Images NDC 23155-263

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 Hydrochloride (NDC 23155-263). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Heritage Pharmaceuticals Inc. D/b/a Avet Pharmaceuticals 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

Structure (78c29d1d 9b3a 4474 B8c8 3db346de689f 01)

Structure (78c29d1d 9b3a 4474 B8c8 3db346de689f 01)
Chemical structure of Diphenhydramine Hydrochloride showing the molecular arrangement including two benzene rings connected by an ether linkage to a dimethylaminoethyl side chain with associated hydrochloride (HCl) molecule.*
FDA Label Image
FDA Label Image

Carton-label (Carton Label)

Carton-label (Carton Label)
Packaging label for DiphenhydramINE Hydrochloride Injection, USP, 500 mg/10 mL (50 mg/mL) by Avet Pharmaceuticals Inc. It is a 10 mL multi-dose vial labeled for deep intramuscular or slow intravenous use. The label notes high potency, sterile pyrogen-free solution, storage instructions, and manufacturing details including Avet Pharmaceuticals Inc. and Maiva Pharma Private Limited.*
FDA Label Image

Vial-label (Vial Label)

Vial-label (Vial Label)
Label for Diphenhydramine Hydrochloride Injection, USP 50 mg/mL (500 mg/10 mL) multi-dose vial. The label indicates the product is for intramuscular or intravenous use and is classified as high potency. Manufactured by Maiva Pharma Private Limited for Avet Pharmaceuticals Inc., the label includes storage instructions and barcodes along with the Avet Pharma logo.*

* 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.