Ibuprofen Tablet, Film Coated
Product Images NDC 69367-394

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 Ibuprofen (NDC 69367-394). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Westminster Pharmaceuticals, 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

Chemical Structure (Ibuprophen 01)

Chemical Structure (Ibuprophen 01)
Chemical structure of ibuprofen, showing a benzene ring substituted with an isobutyl group and a carboxylic acid functional group.*
FDA Label Image

Principal Display Panel (400 mg Tablet Bottle Label)

Principal Display Panel (400 mg Tablet Bottle Label)
Label for Ibuprofen Tablets, USP 400 mg, film-coated oral tablets from Westminster Pharmaceuticals, LLC. The label shows the product name, strength (400 mg), quantity (500 tablets), and storage instructions. It includes manufacturer and barcode details, along with a link to the printed medication guide at www.wprx.com/prescription-catalog.*
FDA Label Image

Principal Display Panel (600 mg Tablet Bottle Label)

Principal Display Panel (600 mg Tablet Bottle Label)
Ibuprofen Tablets USP 600 mg film-coated tablets. The label indicates a package quantity of 500 tablets, manufactured for Westminster Pharmaceuticals, LLC. It includes dosage instructions, storage conditions, and barcode. Manufactured by Shandong Xinhua Pharmaceutical Co., Ltd., China, the label is predominantly brown, white, and green with clear branding.*
FDA Label Image

Principal Display Panel (800 mg Tablet Bottle Label)

Principal Display Panel (800 mg Tablet Bottle Label)
Label for Ibuprofen Tablets, USP 800 mg film coated tablets. The package contains 500 tablets and is labeled for prescription use only by Westminster Pharmaceuticals, LLC. Dosage and storage instructions are provided, including storage temperature and warnings to keep out of reach of children. The label includes the NDC 69367-396-05 and manufacturer details for Shandong Xinhua Pharmaceutical Co., Ltd., China.*

* 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.