Ibuprofen
Product Images NDC 76168-095

3 FDA label images from Velocity Pharma · 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 76168-095). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Velocity Pharma, 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_200ct (Ibu 200ct)

Ibu_200ct (Ibu 200ct)
Ibuprofen 200 mg tablets packaging label from Velocity Pharma. The label prominently features the product name 'Ibuprofen' and indicates it is for pain relief/fever reduction. It includes a barcode, active ingredient information, usage directions, warnings, and other drug facts. The design includes a red circle highlighting "200 Tablets" and blue background panels with yellow and white text.*
FDA Label Image

Ibu_24ct (Ibu 24ct)

Ibu_24ct (Ibu 24ct)
Packaging label for Ibuprofen tablets 200 mg by Velocity Pharma. The label states the product is for Pain Reliever/Fever Reducer with 24 tablets per bottle. The label includes Drug Facts such as active ingredient information, uses, warnings, directions, other information, and inactive ingredients. The label also provides a barcode and manufacturer details.*
FDA Label Image

Ibu_30ct (Ibu 30ct)

Ibu_30ct (Ibu 30ct)
Packaging label for Ibuprofen 200 mg tablets by Velocity Pharma. The label indicates the product is a pain reliever and fever reducer with 30 tablets per bottle. The label includes standard Drug Facts panels with active ingredient, uses, warnings, directions, and inactive ingredients information.*

* 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.