Ibuprofen
Product Images NDC 61919-125

3 FDA label images from Direct Rx · 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 61919-125). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Direct Rx, 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

124 (124 30)

124 (124 30)
Packaging label for IBUPROFEN 400mg tablets by Direct Rx. The label indicates a bottle containing 30 count tablets, generic for MOTRIN, with usage warnings including potential drowsiness or dizziness. The label includes lot and expiration information, and storage instructions emphasizing keeping out of reach of children.*
FDA Label Image

125 (125 30)

125 (125 30)
IBUPROFEN 600 mg 30 tablets label from Direct Rx. The label indicates the product is a generic for Motrin, with each film-coated tablet containing 600 mg ibuprofen USP. The packaging details include lot number and expiration date, with warnings about drowsiness or dizziness and caution to keep out of reach of children. The product is packaged and distributed by Direct Rx in Alpharetta, GA.*
FDA Label Image

126 (126 30)

126 (126 30)
The label is for IBUPROFEN 800 mg tablets, packaged in a bottle of 30 tablets. It lists the generic for Motrin and states each film-coated tablet contains ibuprofen USP 800 mg. The label includes packaging and distribution information by Direct Rx, lot numbers, expiration dates, and a warning about potential drowsiness or dizziness. The label also advises to keep out of reach of children and to discard after 08/18.*

* 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.