Acetaminophen Tablet, Extended Release
Product Images NDC 21130-108

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 21130-108). 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.

Product Images & Figures Index

FDA Label Image

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

Package Label-principal Display Panel (650 mg (24 Tablets Bottle))
Packaging label for Signature Care Arthritis Pain Reliever Acetaminophen Extended-Release Tablets USP, 650 mg, with 225 extended-release tablets in the package. The label highlights it as an 8-hour pain reliever and fever reducer, distributed by Better Living Brands, LLC. It includes usage instructions, warnings, active ingredient details, and storage information.*
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 Acetaminophen 650 mg extended-release tablets by Better Living Brands, LLC. The label is predominantly red with yellow and white text, featuring the product name "8 Hour Arthritis Pain Reliever." The package contains 225 tablets and highlights the product as a pain reliever and fever reducer. The label includes Drug Facts, warnings, directions, inactive ingredients, and distributor information, as well as a barcode and a note comparing the product to Tylenol 8HR Arthritis Pain.*

* 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.