Diphenhydramine Hydrochloride
Product Images NDC 0904-5306

View Photos of 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 0904-5306). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Major Pharmaceuticals, 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

0835 1000c Label

0835 1000c Label
Banophen 25 mg capsules label by Major Pharmaceuticals. The label indicates it is a complete allergy medication containing Diphenhydramine HCl. It displays a pink and white capsule image and specifies 1000 capsules in the package. The label highlights its use as an antihistamine for relief of upper respiratory allergies and hay fever symptoms.*
FDA Label Image

0835 24bb 4658 Ifc Major Banophen

0835 24bb 4658 Ifc Major Banophen
Banophen 25 mg capsules packaging label showing a 24-capsule carton by Major Pharmaceuticals. The label highlights diphenhydramine hydrochloride 25 mg as the active ingredient, indicates its use as an antihistamine for temporary relief of hay fever and upper respiratory allergy symptoms, and provides dosage instructions, warnings, and inactive ingredients. The packaging also compares Banophen to the active ingredient of Benadryl.*
FDA Label Image

0836 100bc Label

0836 100bc Label
Banophen 50 mg caplets packaging label by Major Pharmaceuticals. The label shows sodium diphenhydramine HCl as the active ingredient in unit dose capsules. The package includes 100 capsules and prominently displays the Major Pharmaceuticals logo. Additional text includes drug facts, warnings, directions, and storage information.*

* 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.