Ibu Tablet
Product Images NDC 66267-964

3 FDA label images from Nucare Pharmaceuticals Inc. · 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 66267-964). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare 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

Pdp (66267 964 00 D55)

Pdp (66267 964 00 D55)
The label for NuCare Pharmaceuticals Inc. Ibuprofen 600 mg oral tablets contains 100 tablets per package. It displays NDC 66267-964-00 and product number R0284100. The label includes warnings to keep out of reach of children and store at controlled temperature. It indicates the product is Rx only.*
FDA Label Image

Strucuture (Structure)

Strucuture (Structure)
Chemical structure of ibuprofen showing a benzene ring with isobutyl and propionic acid side chains, corresponding to the active ingredient ibuprofen in IBU 600 mg oral tablets by NuCare Pharmaceuticals Inc.*
FDA Label Image

Table (Table)

Table (Table)
A data table listing adverse reactions associated with IBU (ibuprofen) tablets. The table categorizes reactions by body system and shows incidence greater than 1% but less than 3%, probable causal relationship with unknown precise incidence, and unknown causal relationship with unknown precise incidence. 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.