Theraprofen-90
Product Images NDC 68405-088

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Theraprofen-90 (NDC 68405-088). 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 600mg (Ibuprofen 600mg)

Label for Ibuprofen 600 mg tablet by Amneal Pharmaceuticals, lot IBO601QY, expiring 02/11, with a 60-count package. The label advises to take as directed by a doctor or see the outsert for dosage. It references Motrin with a manufacturer NDC 53746-0465-05.*

FDA Label Image

Structural Formula Ibuprofen (Strformulaibuprofen)

Chemical structure of the active ingredient for Theraprofen-90, showing a benzene ring with isobutyl and propionic acid side chains consistent with ibuprofen.*

FDA Label Image

Theramine 90 (Theramine90)

Label for Theraprofen-90, an Rx-only medical food by Physician Therapeutics LLC, containing 90 capsules. The label includes directions for use, storage instructions, a warning to keep out of children's reach, and a list of ingredients featuring a proprietary amino acid blend and other components. The design features the Physician Therapeutics logo and product name "THERAMINE."*

FDA Label Image

Theraprofen 90 (Theraprofen90)

Packaging label of Theraprofen-90 co-pack by Physician Therapeutics LLC. The label lists Theramine 90 capsules and Ibuprofen 600 mg, 60 tablets. It states 'Rx Only' and includes the NDC number 68405-088-36. The label features the Physician Therapeutics logo and notes no refills without physician authorization.*

* 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.