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

20ct (Gch 20ct)

Packaging label for Acetaminophen Diphenhydramine HCl Extra Strength Pain Relief PM tablets by Granules USA, Inc. The label shows 20 caplets per package with 500 mg acetaminophen and 25 mg diphenhydramine HCl per caplet. It includes barcode, drug facts, warnings, directions, and manufacturer information. The label states the product is a nighttime sleep-aid and non-habit forming.*

FDA Label Image

50ct (Gch 50ct)

Acetaminophen Diphenhydramine HCl Extra Strength Pain Relief PM caplets, 50 count carton by Granules USA, Inc. The label states active ingredients: acetaminophen USP 500 mg as pain reliever and diphenhydramine HCl 25 mg as nighttime sleep-aid. The package is red with white and blue text, including warnings, directions, drug facts, and barcodes. It also notes that it is made in India.*

FDA Label Image

150ct (Gch 150ct)

Packaging label for Acetaminophen Diphenhydramine HCl Extra Strength Pain Relief PM Caplets. The label displays the product name with active ingredients acetaminophen USP 500 mg and diphenhydramine HCl USP 25 mg. It is a nighttime sleep-aid pain reliever in capsule-shaped caplet form. The package contains 150 caplets. Labeler is Granules USA, Inc. The label includes Drug Facts including uses, warnings, directions, and other consumer information, along with barcoding and size dimensions of 6.5 inches wide.*

* 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.