Acetaminophen Tablet, Extended Release
Product Images NDC 58602-730

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Acetaminophen (NDC 58602-730). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurohealth 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 (250 Tablet Bottle))

Acetaminophen Extended-Release Tablets USP 650 mg by Aurohealth LLC. The label indicates 225 tablets, extended-release film-coated for oral use. Contains warnings, directions, and the NDC 58602-730-28. It is an 8-hour arthritis pain reliever and fever reducer, labeled as containing no aspirin, with caution about other medicines containing acetaminophen.*

FDA Label Image

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

Box packaging label for Acetaminophen Extended-Release Tablets USP, 650 mg by Aurohealth LLC. The label states it is an 8-hour arthritis pain relief, pain reliever/fever reducer for temporary relief of minor arthritis pain. The package contains 225 extended-release tablets. It includes warnings, directions, and inactive ingredients, as well as usage and safety information. The label also displays the NDC 58602-730-28 and a barcode.*

* 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.