Acetaminophen Tablet, Extended Release
Product Images NDC 69842-037

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 69842-037). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cvs Pharmacy, Inc., 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))
ITCH REL SPR CVS 650 mg extended-release acetaminophen tablets packaging label. The yellow and white label indicates 150 tablets for 8-hour arthritis pain relief, manufactured by CVS. The label contains Drug Facts detailing uses, warnings, and directions, with instructions to push down and turn the cap to open. Prominent warnings include not using with other acetaminophen products and consulting a doctor for certain conditions.*
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))
The image shows the packaging label for CVS Health 8HR Arthritis Pain Relief tablets containing acetaminophen USP 650 mg. It is an extended-release tablet format with 150 tablets per package. The label highlights its use as a pain reliever and fever reducer for temporary relief of minor arthritis pain. The package is yellow with red and blue text, a CVS Health logo, and includes drug facts and usage information along with a depiction of the tablet's actual size.*

* 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.