Ibu
Product Images NDC 50090-4341

3 FDA label images from A-s Medication Solutions · 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 50090-4341). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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 (Lbl500904341)

Label Image (Lbl500904341)
IBU 800 mg tablet bottle label from A-S Medication Solutions. The label includes dosage information stating each tablet contains 800 mg of ibuprofen, storage instructions to keep at room temperature and avoid excessive heat, and packaging details for 30 tablets. The NDC number 50090-4341-0 is shown along with lot and product numbers.*
FDA Label Image

Strucuture (Structure)

Strucuture (Structure)
Chemical structure diagram of the active ingredient in IBU, showing the molecular arrangement with a benzene ring attached to an isobutyl group and a carboxylic acid functional group.*
FDA Label Image

Table (Table)

Table (Table)
A data table presenting adverse reactions categorized by organ system for the drug IBU. The table specifies incidence rates as greater than 1% but less than 3%, probable causal relationships, and precise incidence unknown with both probable and unknown causal relationships. It includes reactions in gastrointestinal, central nervous system, dermatologic, special senses, hematologic, metabolic/endocrine, cardiovascular, allergic, renal, and miscellaneous categories, along with footnotes clarifying the classification of 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.