Acetaminophen And Ibuprofen Tablet, Film Coated
Product Images NDC 58602-893

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Acetaminophen And Ibuprofen (NDC 58602-893). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurohealth Llc, 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

Package Label-principal Display Panel (250 mg/125 mg (10 Caplets Bottle))

Label for Acetaminophen and Ibuprofen tablets 250 mg/125 mg by Aurohealth LLC, containing 10 capsule-shaped film-coated tablets. The label includes the product's active ingredients, purpose as a pain reliever, and warnings about acetaminophen liver damage and NSAID stomach bleeding. Directions and inactive ingredients are also detailed, with contact information for questions. The NDC code 58602-893 is shown.*

FDA Label Image

Package Label-principal Display Panel (250 mg/125 mg Container Carton (10 Caplets))

The packaging label for Acetaminophen and Ibuprofen tablets contains 10 film-coated caplets with strengths of 250 mg acetaminophen and 125 mg ibuprofen. The label highlights the product as a dual action pain reliever, distributed by Aurohealth LLC. It includes detailed Drug Facts covering active ingredients, uses, warnings, directions, and storage instructions.*

FDA Label Image

Package Label-principal Display Panel (250 mg/125 mg Blister Carton (2 Caplets))

Acetaminophen and Ibuprofen (NSAID) 250 mg/125 mg film-coated tablets packaging label by Aurohealth LLC. The carton contains 2 capsule-shaped tablets and is labeled as a pain reliever for headache, muscular aches, menstrual cramps, toothache, and minor arthritis pain. The label includes Drug Facts detailing active ingredients, warnings, directions, and storage instructions. The product NDC is 58602-893-61.*

* 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.