Acetaminophen And Diphenhydramine Hydrochloride Tablet
Product Images NDC 30142-193

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Acetaminophen And Diphenhydramine Hydrochloride (NDC 30142-193). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kroger Company, 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

Package Label-principal Display Panel 100 Caplets (Aurophen Fig1)

Package Label-principal Display Panel 100 Caplets (Aurophen Fig1)
Packaging label for Acetaminophen PM Extra Strength Gelcaps by Kroger Company. Contains Acetaminophen USP 500 mg and Diphenhydramine Hydrochloride USP 25 mg per capsule. The label indicates the product is a pain reliever and nighttime sleep-aid with rapid release and is non-habit forming. The container holds 50 gelcaps, with warnings, directions, and manufacturer information also visible.*
FDA Label Image

Package Label-principal Display Panel 500 mg / 25 mg (50 Caplets Bottle Carton) (Aurophen Fig2)

Package Label-principal Display Panel 500 mg / 25 mg (50 Caplets Bottle Carton) (Aurophen Fig2)
Packaging label for Acetaminophen and Diphenhydramine hydrochloride Extra Strength PM tablets, containing 500 mg acetaminophen and 25 mg diphenhydramine hydrochloride per tablet. The label shows the product in a 50 count bottle form, distributed by The Kroger Co. The label includes various drug facts, warnings, directions, inactive ingredients, barcode, 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.