Acetaminophen Tablet, Film Coated, Extended Release
Product Images NDC 0363-9992

3 FDA label images from Walgreens · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Acetaminophen (NDC 0363-9992). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Walgreens, 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

200000003691 24ct Muscle Pain

200000003691 24ct Muscle Pain
Packaging label for Walgreens Acetaminophen 650 mg extended-release film-coated tablets. The label features the product name, strength, and dosage form with 8-hour pain relief claimed. It includes Drug Facts panels detailing active ingredients, uses, warnings, directions, and storage information. The labeler is Walgreens, and the product is intended for oral use.*
FDA Label Image

200000003693 100ct Muscle Pain

200000003693 100ct Muscle Pain
Packaging label for Walgreens 8-Hour Pain Reliever Acetaminophen 650 mg extended-release film-coated tablets. The package contains 100 caplets and highlights the product as a muscle pain reliever providing up to 8 hours of relief. The label displays drug facts, usage instructions, active ingredient details, warnings, and manufacturer information.*
FDA Label Image

200000003695 200ct Muscle Pain

200000003695 200ct Muscle Pain
Walgreens 8-Hour Pain Reliever 650 mg extended-release film-coated tablets, 200 count, oral use. The label indicates the active ingredient as acetaminophen with a muscle pain relief purpose for up to 8 hours. The packaging includes drug facts and directions for use, with a Walgreens brand labeler and product NDC 0363-9992.*

* 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.