Acetaminophen And Ibuprofen Tablet, Film Coated
Product Images NDC 69452-394

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Acetaminophen And Ibuprofen (NDC 69452-394). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bionpharma 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

Back Ply-2 (Backply 2)

This image shows a Drug Facts panel continuation for an acetaminophen and ibuprofen combination tablet. It details warnings to stop use and consult a doctor for symptoms like stomach bleeding or heart problems, directions for dosing by age including not exceeding 6 tablets in 24 hours, storage instructions, and a list of inactive ingredients. Contact information for questions or comments is also provided.*

FDA Label Image

Back Ply -1 (Backply)

Drug Facts panel continuation for Acetaminophen and Ibuprofen tablets highlighting allergy warnings for acetaminophen and NSAIDs, stomach bleeding warnings, heart attack and stroke risks, and usage precautions including when to avoid or consult a doctor before use. It includes advice on taking the product with food or milk if stomach upset occurs.*

FDA Label Image

Front (Front)

Label for a+health acetaminophen and ibuprofen (NSAID) tablets, 250 mg/125 mg, film coated caplets. The label highlights the product as a dual action pain reliever with 216 caplets per container. It includes drug facts listing acetaminophen USP 250 mg and ibuprofen USP 125 mg as active ingredients for pain relief. The label warns against use with other acetaminophen products due to liver damage risk. Distributed by Bionpharma Inc., Princeton, NJ, made in India.*

* 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.