Theraprofen-800
Product Images NDC 68405-188

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Theraprofen-800 (NDC 68405-188). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Physician Therapeutics Llc, 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

Ibuprofen 800mg (Ibuprofen 800mg)

The label is for Ibuprofen 800 mg tablets, indicating a quantity of 30 tablets. It includes the lot number IUB837QY and expiration date 01/13. The manufacturer is listed as Amneal Pharmaceuticals. The label also references a comparison to Motrin with manufacturer NDC 53746-0466-05. Directions advise to take as directed by a doctor or see outer packaging for usual dosage information. Multiple barcodes and repeating small labels are present on the right side.*

FDA Label Image

Ibuprofen 800 mg Structural Formula (Ibuprofen800mgstructuralformula)

Chemical structure of the active ingredient in Theraprofen-800, showing a benzene ring with an isobutyl group on one side and a propionic acid group on the other.*

FDA Label Image

Theramine 90 (Theramine90)

This label panel for Theraprofen-800 medical food capsules includes directions for use stating the product must be administered under medical supervision for adults. It details storage instructions, warnings, a proprietary amino acid blend Ingredients list, and other non-active components. The product is distributed by Physician Therapeutics LLC in Los Angeles, CA.*

FDA Label Image

Theraprofen 800 (Theraprofen800)

Label for Theraprofen-800, a medical co-pack by Physician Therapeutics LLC. The label highlights two components: Theramine 90 capsules and Ibuprofen 800 mg, 30 tablets. It includes a medical symbol logo in the center and states 'Rx Only' with NDC 68405-188-36 for this co-pack, along with a note on physician authorization for refills.*

* 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.