Acetaminophen Diphenhydramine Hcl Tablet
Product Images NDC 69848-014

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Acetaminophen Diphenhydramine Hcl (NDC 69848-014). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Granules Usa, 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

20 Count (300000417 R 00 Final)

Packaging label for Acetaminophen Diphenhydramine HCl Extra Strength Pain Relief PM caplets, containing 500 mg acetaminophen and 25 mg diphenhydramine HCl per caplet. The label shows a red carton with drug facts panels, warnings, and instructions. The product contains 20 caplets and is distributed by Granules USA, Inc.*

FDA Label Image

50 Count (300000458 R 00 Final)

The packaging label for Acetaminophen Diphenhydramine HCl Extra Strength Pain Relief PM tablets, containing 50 caplets. The label highlights active ingredients acetaminophen USP 500 mg and diphenhydramine HCl USP 25 mg per caplet. Manufactured by Granules USA, Inc., the label features usage warnings, directions, inactive ingredients, and storage instructions, with prominent branding and a red background.*

FDA Label Image

150 Count (300000460 R 00 Final)

Packaging label for Acetaminophen Diphenhydramine HCl Extra Strength Pain Relief PM tablets, containing 150 caplets. The label shows active ingredients acetaminophen 500 mg and diphenhydramine HCl 25 mg. It is a nighttime sleep-aid and pain reliever, non-habit forming. The label includes the Granules USA, Inc. logo, drug facts, usage instructions, and a barcode. The tablets are capsule-shaped and blue.*

* 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.