Ibu Tablet
Product Images NDC 63187-614

3 FDA label images from Proficient Rx Lp · 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 63187-614). 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

63187-614-28 (63187 614 15)

63187-614-28 (63187 614 15)
Label for Ibuprofen 600 mg tablets, quantity 28, from Proficient Rx LP. The label includes the NDC 63187-614-28 and states Rx Only. The tablets are described as white caplets, debossed 6I, containing Ibuprofen USP 600 mg each. Manufacturer is Dr. Reddy's Laboratories LA, LLC, Shreveport, LA. Storage instructions and safety warnings are also included.*
FDA Label Image

Strucuture (Structure)

Strucuture (Structure)
Chemical structure diagram of ibuprofen, showing the molecular formula with a benzene ring, carboxylic acid group, and isobutyl side chains, consistent with the generic name ibuprofen.*
FDA Label Image

Table (Table)

Table (Table)
A multi-column table listing adverse reactions categorized by organ system and their incidence rates for IBU (Ibuprofen) tablets 600 mg. It classifies reactions by probable causal relationship and incidence rates: greater than 1% but less than 3%, precise incidence unknown but less than 1%, 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.*

* 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.