Acetaminophen Tablet
Product Images NDC 70010-161

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Acetaminophen (NDC 70010-161). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Granules Pharmaceuticals 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

100-count-bottle-carton-label (100 Carton)

Packaging label for ACETAMINOPHEN Extra Strength Tablets USP 500 mg by Granules Pharmaceuticals Inc. The label indicates 100 caplets, described as capsule-shaped tablets, for pain relief and fever reduction in adults. The label includes the product NDC 70010-161-01 and shows the Acetaminophen name prominently in black and blue text with additional drug facts and barcode details.*

FDA Label Image

100-count-bottle-label (100 Caplets)

Label for ACETAMINOPHEN 500 mg Tablets USP by Granules Pharmaceuticals Inc., an over-the-counter oral pain reliever and fever reducer. The label shows an image of a white, capsule-shaped tablet and indicates a bottle containing 100 caplets. The label includes drug facts with active ingredient information and usage directions for adults.*

FDA Label Image

500-count-bottle-label (500 Caplets)

Packaging label for Extra Strength Acetaminophen Tablets USP 500 mg by Granules Pharmaceuticals Inc. The label shows 500 caplets (capsule-shaped tablets) as a pain reliever and fever reducer for adults. The label includes drug facts such as active ingredient, purposes, uses, warnings, directions, and inactive ingredients. The product NDC is 70010-161-05 and the label indicates it contains no aspirin.*

* 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.