Ibuprofen Tablet, Film Coated
Product Images NDC 51655-474

View Photos of 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 51655-474). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, 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

Label (51655 474 52 Master Bottle Label Approval Rev A 01 21)

Label (51655 474 52 Master Bottle Label Approval   Rev A 01 21)
Label for Ibuprofen tablets USP 600 mg oral film-coated tablets. The bottle contains 30 tablets and is Rx only. Storage instructions specify controlled room temperature (68°-77°F) and keeping out of reach of children in the original container. Labeler is Northwind Health Company, LLC.*
FDA Label Image

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

Medguide Ibuprofen Tablets (Medication Guide For Nonsteroidal Anti Inflammatory Drugs)
A medication guide text panel for Nonsteroidal Anti-Inflammatory Drugs (NSAIDs) describing important safety information, risks, side effects, and precautions related to NSAID use. It provides warnings about heart attack, stroke, bleeding, interactions, and who should avoid NSAIDs. Instructions for patients to contact healthcare providers with symptoms and general NSAID information are included. The guide notes manufacturing details for Time-Cap Labs, Inc. and Marksans Pharma Ltd.*

* 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.