Ibuprofen
Product Images NDC 53808-0436

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ibuprofen (NDC 53808-0436). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by State Of Florida Doh Central 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

Principal Display Panel 400 mg (Ibuprofen 400mg(major))

Label of Ibuprofen 400 mg tablets from State of Florida DOH Central Pharmacy. The label shows a quantity of 30 tablets, prescription only status, lot number HA27309, and an expiration date of June 30, 2010. The label includes a barcode and identifies the package origin as Tallahassee, FL 32304.*

FDA Label Image

Principal Display Panel 600mg (Ibuprofen 600mg(major))

Label for Ibuprofen 600 mg tablets, quantity 30, prescription only. Labeled by State of Florida DOH Central Pharmacy, Tallahassee, FL. Contains lot number and expiration date, with barcode and UPC. Packaging information is printed including internal pharmacy codes.*

FDA Label Image

Principal Display Panel 800 mg (Ibuprofen 800mg(major))

Label for Ibuprofen 800 mg tablets, prescription only, quantity of 30 tablets. The label includes lot number HE10209, an expiration date of 06/30/10, and is packaged by the State of Florida DOH Central Pharmacy in Tallahassee, FL. The label also shows a barcode and UPC# 309045187401.*

FDA Label Image

Chemical Structure (Ibuprofen 1)

Chemical structure of ibuprofen showing its molecular arrangement with labeled carbon and functional groups, including a carboxylic acid (COOH) moiety and isobutyl side chain attached to a benzene ring.*

* 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.