Acetaminophen
Product Images NDC 71399-8025

3 FDA label images from Akron Pharma Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Acetaminophen (NDC 71399-8025). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Akron Pharma 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

325mg-1000 (325mg 1000ct)

325mg-1000 (325mg 1000ct)
Acetaminophen 325 mg tablets in regular strength by Akron Pharma. The white label indicates 1000 tablets with aspirin-free pain reliever/fever reducer. Packaging includes warnings, uses, and dosing instructions, with child-resistant packaging noted. Manufactured in the USA. Contains a barcode and the Akron Pharma logo.*
FDA Label Image

325mg-100 (325mg 100ct)

325mg-100 (325mg 100ct)
Drug Facts panel for Acetaminophen 325 mg tablets by Akron Pharma Inc. Lists active ingredient, uses, warnings including liver damage risk, allergy alert, and overdose warning. Provides directions by age group, storage info, inactive ingredients, and a contact number for questions. Notes child-resistant packaging and manufacturing details.*
FDA Label Image

325mg-50 (325mg 50ct)

325mg-50 (325mg 50ct)
Drug Facts panel for Acetaminophen 325 mg tablets by Akron Pharma Inc. Details active ingredient, uses, warnings including liver warning and allergy alert, directions for adults and children, overdose warnings, inactive ingredients, and manufacturer contact information. The label emphasizes it is aspirin-free and a pain reliever/fever reducer, with 50 tablets per container.*

* 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.