Ibuprofen Tablet, Film Coated
Product Images NDC 60760-603

2 FDA label images from St. Mary's Medical Park Pharmacy · 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 Ibuprofen (NDC 60760-603). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by St. Mary's Medical Park Pharmacy, 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 (Ibuprofen 60760 603 60)

Ibu (Ibuprofen 60760 603 60)
Label for IBUPROFEN 600 mg film-coated tablets, USP, with a quantity of 60 tablets. The label includes NDC 60760-603-60 and indicates the product is manufactured by Marksans Pharma Ltd., Goa, India, and packaged by St. Mary's Medical Park Pharmacy in Oro Valley, AZ. Storage instructions specify controlled room temperature between 15°-30°C (59°-86°F). Expiration date and lot number are not visible.*
FDA Label Image

Medguide Ibuprofen Tablets (Medication Guide For Nonsteroidal Anti Inflammatory Drugs)

Medguide Ibuprofen Tablets (Medication Guide For Nonsteroidal Anti Inflammatory Drugs)
This image displays a Medication Guide for Nonsteroidal Anti-Inflammatory Drugs (NSAIDs). It covers important safety information including risks of heart attack, stroke, bleeding, and ulcers, usage cautions, possible side effects, and advice on who should not take NSAIDs. Additional details include instructions to consult healthcare providers regarding medical conditions and medication interactions. The guide is approved by the U.S. Food and Drug Administration and includes manufacturing and labeling details.*

* 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.