Acetaminophen And Diphenhydramine Hydrochloride Tablet
Product Images NDC 21130-224

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 21130-224). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Better Living Brands, Llc, 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 500 mg / 25 mg (20 Caplets Bottle) (Aurophen Fig1)

Package Label-principal Display Panel 500 mg / 25 mg (20 Caplets Bottle) (Aurophen Fig1)
Packaging label for Signature Care Extra Strength Pain Relief PM Gelcaps containing 500 mg Acetaminophen and 25 mg Diphenhydramine Hydrochloride. The label highlights the product as a pain reliever and nighttime sleep aid, non-habit forming, and rapid release. The package contains 20 gelcaps and is labeled by Better Living Brands, LLC.*
FDA Label Image

Package Label-principal Display Panel 500 mg / 25 mg (20 Caplets Bottle Carton) (Aurophen Fig2)

Package Label-principal Display Panel 500 mg / 25 mg (20 Caplets Bottle Carton) (Aurophen Fig2)
Carton label for Acetaminophen and Diphenhydramine hydrochloride Extra Strength Pain Relief PM gelcaps, containing 500 mg acetaminophen and 25 mg diphenhydramine hydrochloride per gelcap. The package includes 20 non-rabbit forming gelcaps, distributed by Better Living Brands, LLC. The label highlights pain relief and nighttime sleep aid uses with warnings, inactive ingredients, and storage instructions.*

* 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.