Ibuprofen
Product Images NDC 50436-0321

4 FDA label images from Unit Dose Services · 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 50436-0321). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Unit Dose Services, 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

Ibuprofen-structure (Ibuprofen Structure)

Ibuprofen-structure (Ibuprofen Structure)
Chemical structure of Ibuprofen showing a benzene ring with attached isobutyl and propanoic acid groups.*
FDA Label Image

Lbl504360319

Lbl504360319
Ibuprofen 400 mg, film-coated tablets, packaged as 30 tablets. The label shows the NDC 50436-0319-1 and is manufactured by Granules India Limited in Hyderabad, India. The product is labeled for prescription use only and is distributed by Unit Dose Services, L.C.C., Dania, FL.*
FDA Label Image

Label Image (Lbl504360321)

Label Image (Lbl504360321)
Ibuprofen 800 mg film-coated tablets, 30 count, labeled by Unit Dose Services. The packaging indicates manufacture by Granules India Ltd, Hyderabad, India. The label features NDC 50436-0321-1, storage instructions, and a warning to keep out of reach of children, with Rx only designation.*
FDA Label Image

Lbl504363200

Lbl504363200
Label for Ibuprofen 600 mg tablets, packaged as 30 tablets, labeled by Unit Dose Services. The label includes manufacturer information for Granules India Limited, with packaging and storage instructions, dosage form as film-coated tablets, and prescription-only designation. The label lists storage and warning details and multiple NDC codes corresponding to the product.*

* 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.