Acetaminophen Tablet, Extended Release
Product Images NDC 0363-9604

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 (NDC 0363-9604). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Walgreen Co., 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 (650 mg (250 Tablet Bottle))

Package Label-principal Display Panel (650 mg (250 Tablet Bottle))
Packaging label for Walgreens Acetaminophen Extended-Release Tablets USP, 650 mg, oral tablets. The label states the product is an arthritis pain reliever and fever reducer with an 8-hour duration. The package contains 24 extended-release tablets. The label includes warnings, active ingredients, use instructions, and a tamper-evident seal notice. The labeler is Walgreens Co.*
FDA Label Image

Package Label-principal Display Panel (650 mg (250 Tablets Container Carton))

Package Label-principal Display Panel (650 mg (250 Tablets Container Carton))
Acetaminophen 650 mg extended-release tablets packaging label for arthritis pain relief by Walgreen Co. The red and white carton shows 24 tablets per package. Drug Facts panels detail the active ingredient, uses, warnings, directions, and inactive ingredients. The label states no aspirin, includes storage instructions, and contact information. Distributed by Walgreen Co., made in India.*

* 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.