Ibu Tablet
Product Images NDC 71205-604

View Photos of 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 Ibu (NDC 71205-604). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

71205-604-30 (400mg100)

71205-604-30 (400mg100)
Label for IBU Ibuprofen 400 mg oral tablets, containing 30 tablets. The label indicates the active ingredient ibuprofen USP 400 mg in each white, oval tablet. The product is labeled for prescription use only, manufactured by Dr. Reddy's Laboratories LA LLC and packaged by Proficient Rx LP in Thousand Oaks, CA. Storage instructions advise keeping at room temperature and avoiding heat above 40°C.*
FDA Label Image

Strucuture (Structure)

Strucuture (Structure)
Chemical structure of Ibuprofen showing the molecular arrangement including isobutyl and carboxylic acid functional groups attached to a phenyl ring.*
FDA Label Image

Table (Table)

Table (Table)
Table listing adverse reactions associated with ibuprofen (IBU) tablets, categorized by body system. It details incidences greater than 1% (but less than 3%) under probable causal relationship, precise incidence unknown but less than 1% under probable causal relationship, and reactions with precise incidence unknown and causal relationship unknown. Categories include gastrointestinal, central nervous system, dermatologic, special senses, hematologic, metabolic/endocrine, cardiovascular, allergic, renal, and miscellaneous.*

* 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.