Trepoxen-250
Product Images NDC 68405-018

4 FDA label images from Physician Therapeutics Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Trepoxen-250 (NDC 68405-018). 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

Chemical Structure Naproxen (Chemstrnaproxen)

Chemical Structure Naproxen (Chemstrnaproxen)
Chemical structure diagram of the active ingredient naproxen, showing molecular components and formula C14H14O3 with a molecular weight of 230.26.*
FDA Label Image

Naproxen 250mg (Naproxen 250mg)

Naproxen 250mg (Naproxen 250mg)
Label for Naproxen 250 mg tablets showing lot number NX202QY, manufacturer AMNEALPHRM, expiration date 01/13, and a quantity of 30 tablets. The label includes a comparison reference to Naprosyn with Mfg. NDC 53746-0188-05 and instructions to take as directed by a doctor or see outer label for dosage information. Several smaller identical labels for the same product are also visible on the right side.*
FDA Label Image

Theramine 90 (Theramine90)

Theramine 90 (Theramine90)
This image shows directions for use, storage instructions, a warning, and ingredients for Theramine Medical Food capsules by Physician Therapeutics LLC. Directions specify use under medical supervision for adults, dosing every four hours. Ingredients include a proprietary amino acid blend, various extracts, and other components. The product contains 90 capsules and is labeled Rx only.*
FDA Label Image

Theraproxen (90)

Theraproxen (90)
Theraproxen-90 co-pack label from Physician Therapeutics LLC features Theramine 90 capsules and Naproxen 250 mg 60 tablets. The label emphasizes no refills without physician authorization, includes the proprietary and ingredient names, strengths, forms, and NDC 68405-018-36 for this co-pack.*

* 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.