Aramark Ibuprofen
Product Images NDC 81238-0103

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Aramark Ibuprofen (NDC 81238-0103). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Western First Aid Safety Dba Aramark, 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

0103 100 Tab Box (0103 100 Tab Box)

The image shows the packaging label for Aramark Ibuprofen tablets, an anti-inflammatory fever reducer. The label states the product contains 100 tablets and is manufactured by Western First Aid Safety DBA Aramark in Lenexa, KS. The label includes dosage instructions, warnings, a barcode, and storage information. The package design features black, white, and gray panels, with the 'Ibuprofen' name prominently displayed in bold letters.*

FDA Label Image

0103 2-tab Packet (0103 2 Tab Packet)

Drug Facts label panel for Aramark Ibuprofen Pain Reliever/Fever Reducer tablets, showing active ingredient ibuprofen 200 mg per tablet, uses for temporary relief of minor aches and pains, warnings including stomach bleeding risk, directions for use including dosage limits, other storage information, and contact details for Aramark Lenexa, KS.*

FDA Label Image

0103 250 Tab Box (0103 250 Tab Box)

Packaging label for Aramark Ibuprofen tablets, an anti-inflammatory and fever reducer. The label indicates a bottle containing 250 tablets. It includes Drug Facts panels on multiple sides, the Aramark logo, and manufacturer information for Aramark in Lenexa, KS. The design features black, white, and green colors with red and black text.*

* 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.