Acetaminophen And Ibuprofen Back Pain Tablet
Product Images NDC 70010-213

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Acetaminophen And Ibuprofen Back Pain (NDC 70010-213). 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

Ibu-apap-18s-cont-carton (Ibu Apap 18s Cont Carton)

Ibu-apap-18s-cont-carton (Ibu Apap 18s Cont Carton)
The packaging label for Acetaminophen and Ibuprofen (NSAID) tablets by Granules Pharmaceuticals Inc. features the strength 250 mg/125 mg prominently. It contains 18 capsule-shaped caplets designed for dual-action pain relief, specifically for back pain with up to 8 hours of relief. The label includes NDC 70010-213-26, drug facts, warnings, and directions for use, along with a barcode and lot/expiration information area.*
FDA Label Image

Ibu-apap-18s-cont-labl (Ibu Apap 18s Cont Labl)

Ibu-apap-18s-cont-labl (Ibu Apap 18s Cont Labl)
Drug Facts label for Acetaminophen and Ibuprofen Back Pain tablets 250 mg/125 mg, outlining active ingredients, uses, warnings including liver damage and stomach bleeding warnings, allergy alerts, heart attack and stroke warnings, directions for use, storage instructions, and inactive ingredients. The label emphasizes not using with other acetaminophen-containing drugs and includes contact information for questions.*

* 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.