Acetaminophen Tablet
Product Images NDC 71399-1025

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Acetaminophen (NDC 71399-1025). 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

325-100 (325 100)

325-100 (325 100)
The label for ACETAMINOPHEN 325 MG tablets by Akron Pharma Inc. features a bold red and white design stating "Regular Strength." It contains 100 tablets and is aspirin-free, serving as a pain reliever and fever reducer. The label includes drug facts, warnings about liver damage and allergic reactions, and instructions to consult a doctor before use with liver disease, arthritis, or blood thinning drugs.*
FDA Label Image

325-1000 (325 1000)

325-1000 (325 1000)
Drug Facts label for Acetaminophen 325 mg tablets by Akron Pharma Inc. It includes active ingredient, uses, warnings, directions for different age groups, and other safety information. Details on overdose, allergy alerts, and inactive ingredients gelatinized starch, magnesium stearate, and povidone are also provided. The label warns against use with other acetaminophen-containing products.*
FDA Label Image

325-100ud (325 100ud)

325-100ud (325 100ud)
Carton packaging for Acetaminophen 325 mg tablets by Akron Pharma Inc. It contains 100 regular strength, oral, aspirin-free pain reliever and fever reducer tablets. The label highlights the 325 mg strength and includes warnings, directions, and inactive ingredients. The product NDC is 71399-1025-3.*
FDA Label Image

325-50 (325 50)

325-50 (325 50)
Drug Facts label for Acetaminophen 325 mg tablets by Akron Pharma Inc. This label includes active ingredient information, uses for temporary relief of minor aches and pains, warnings such as liver damage risk, allergy alert, and directions for use. It also advises users to ask a doctor before use if they have certain conditions and not to exceed recommended dosages.*

* 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.