Diphenhydramine
Product Images NDC 61010-4409

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Diphenhydramine (NDC 61010-4409). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Safetec Of America, 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

Principal Display Panel (25 mg Pouch Label)

Label for Diphenhydramine HCl Allergy Relief capsules from Safetec of America, Inc. Each capsule contains 25 mg of diphenhydramine hydrochloride as an antihistamine. The label includes drug facts such as uses to relieve allergy symptoms, warnings, directions for use by age group, and inactive ingredients. It lists packaging storage instructions, cautions for use, and a customer service phone number.*

FDA Label Image

Principal Display Panel – 50 Pouches Carton Label (Dip0e 0001 02)

Packaging label for Diphenhydramine HCl 25 mg capsules by Safetec of America, Inc. The product is marketed as an allergy relief antihistamine with 50 tamper-evident unit dose pouches, each containing 2 capsules. The label highlights relief from itchy watery eyes, sneezing, and runny nose, and includes Drug Facts with active ingredient and usage information.*

FDA Label Image

Principal Display Panel – 100 Pouches Carton Label (Dip0e 0001 03)

Packaging label for Diphenhydramine HCl 25 mg Allergy Relief capsules by Safetec of America, Inc. The label highlights the antihistamine's use for itchy watery eyes, sneezing, and runny nose. The package contains 100 pouches with 2 capsules per pouch and includes tamper-evident unit dose pouches with instructions not to use if damaged.*

* 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.