Ibu
Product Images NDC 53002-3370

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ibu (NDC 53002-3370). 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 (Lbl530023370)

IBU Ibuprofen 400 mg tablets label from RPK Pharmaceuticals, Inc. The white label displays directions to take 1 tablet 4 times a day or as directed by a healthcare provider. It shows patient name, prescription number, lot number, and expiration date fields with barcode. The label indicates 30 tablets per container and includes usage warnings and storage instructions. This is an oral tablet prescription drug packaging label.*

FDA Label Image

Strucuture (Structure)

Chemical structure diagram of the active ingredient ibuprofen, showing its molecular formula with a benzene ring, isobutyl group, and carboxylic acid functional group.*

FDA Label Image

Table (Table)

A table listing adverse reactions categorized by organ system for the medication IBU. It details incidences with greater than 1% but less than 3% probable causal relationship, precise incidence unknown but less than 1% probable causal relationship, and precise incidence unknown with causal relationship unknown. Categories include gastrointestinal, central nervous system, dermatologic, special senses, hematologic, metabolic/endocrine, cardiovascular, allergic, renal, and miscellaneous adverse 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.