Acetaminophen Tablet
Product Images NDC 68001-495

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Acetaminophen (NDC 68001-495). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bluepoint Laboratories, 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

Carton (Acetaminophen Er Tablets Usp Carton 650mg (ndc 68001 495 00) Rev 03 2021)

Acetaminophen 650 mg extended-release tablets package label for arthritis pain by BluePoint Laboratories. The label states the product is an 8-hour pain reliever and fever reducer for temporary relief of minor arthritis pain, contains no aspirin, and includes 100 tablets. The front and sides feature dosage instructions, warnings, inactive ingredients, and manufacturer information.*

FDA Label Image

Label (Acetaminophen Er Tablets Usp Label 650mg (ndc 68001 495 00) Rev 03 2021)

Acetaminophen 650 mg Extended-Release Tablets USP oral tablet label by BluePoint Laboratories. The label highlights 650 mg strength and indicates use as an 8-hour arthritis pain reliever and fever reducer. The package contains 100 extended-release tablets and includes warnings not to use with other medicines containing acetaminophen. The label features detailed drug facts and usage instructions.*

* 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.