Amazon Basic Care Acetaminophen Tablet, Extended Release
Product Images NDC 72288-698

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 Amazon Basic Care Acetaminophen (NDC 72288-698). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amazon.com Services 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 (650 mg (24 Tablets Bottle))

Package Label-principal Display Panel (650 mg (24 Tablets Bottle))
Amazon Basic Care Acetaminophen Extended-Release Tablets USP, 650 mg, oral tablets in a 100-count package. This pain reliever/fever reducer provides up to 8 hours of relief for minor muscle aches and pain. The label includes usage instructions, warnings against use with other acetaminophen-containing medicines, and details about the product's composition and manufacturer, Amazon.com Services LLC.*
FDA Label Image

Package Label-principal Display Panel (650 mg (24 Tablets Container Carton))

Package Label-principal Display Panel (650 mg (24 Tablets Container Carton))
Packaging label for AMAZON BASIC CARE ACETAMINOPHEN Extended-Release Tablets USP, 650 mg. The red box displays the product name, strength, and states it is a pain reliever/fever reducer for up to 8 hours, containing 100 capsule-shaped caplets. The label includes warnings, drug facts, active ingredient details, directions, inactive ingredients, and contact information for Amazon.com Services LLC. The label also compares the product to Tylenol 8HR caplets and includes the NDC 72288-698-10.*

* 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.