Ibu
Product Images NDC 53002-3010

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ibu (NDC 53002-3010). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rpk Pharmaceuticals, 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

Label Image (Lbl530023010)

IBU ibuprofen 600 mg tablets packaging label from RPK Pharmaceuticals, Inc., containing 30 tablets. The label features dosage instructions indicating to take one tablet four times a day or as directed by a practitioner. It includes patient information, lot number, expiration date, barcode, and cautionary statements. The label is marked as prescription only and states ibuprofen as the active ingredient in each tablet.*

FDA Label Image

Label Image (Lbl530023980)

IBU Ibuprofen 800mg Tablets packaging label from RPK Pharmaceuticals, Inc. The label indicates a bottle containing 30 tablets. Directions include taking 1 tablet 3 times a day or as directed. The label includes NDC codes, lot numbers, and placeholders for clinic names.*

FDA Label Image

Strucuture (Structure)

Chemical structure of ibuprofen showing a benzene ring with isobutyl and propionic acid functional groups.*

FDA Label Image

Table (Table)

Table listing adverse reactions associated with IBU, categorized by organ system and incidence rates. Reactions range from gastrointestinal to allergic effects, detailing probable causal relationships and incidence rates less than 1%. Notes explain classification criteria and associations with treatment-related reactions.*

* 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.