Ibuprofen
Product Images NDC 69677-225

3 FDA label images from Mas Management Group, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ibuprofen (NDC 69677-225). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mas Management Group, Inc., 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 800 (Ibu C364e18032714020.pdf Adobe Acrobat Reader Dc 2018 03 27 14.07.56)

Ibu 800 (Ibu C364e18032714020.pdf   Adobe Acrobat Reader Dc 2018 03 27 14.07.56)
Ibuprofen 800mg tablet label by Mas Management Group, Inc., MAS Pharma. The label indicates 20 film-coated tablets per bottle, with details including lot number, expiration date, National Drug Code (NDC) 69677-226-20, and warnings to store in tight, light-resistant container and keep out of reach of children.*
FDA Label Image

Ibuprofen 600 (Skm C364e17083011451.pdf Adobe Acrobat Reader Dc 2017 08 30 11.53.26)

Ibuprofen 600 (Skm C364e17083011451.pdf   Adobe Acrobat Reader Dc 2017 08 30 11.53.26)
Ibuprofen 600mg tablets label from Mas Management Group, Inc. The label indicates a 30-tablet bottle with each film-coated tablet containing 600mg of ibuprofen. It includes lot number, expiration date, NDC code (69677-225-30), drug identification, and storage instructions. The label also bears regulatory and manufacturing details.*
FDA Label Image

Descriptoin (Ibuprofen Structure)

Descriptoin (Ibuprofen Structure)
Chemical structure of ibuprofen showing a benzene ring with isobutyl and carboxyl functional groups attached.*

* 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.