Kortribion Pain Reliever Tablet, Film Coated
Product Images NDC 69729-793

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Kortribion Pain Reliever (NDC 69729-793). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Opmx 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

Kcaps24 (Kortribion W24 Caps 001)

The packaging label for KORTRIBION Pain Reliever tablets contains 24 film-coated caplets formulated with 500 mg Acetaminophen and 65 mg Caffeine as active ingredients. The product is labeled as an analgesic/pain reliever. The label includes usage, warnings, and directions, and displays the OPMX LLC distributor information and Inov Farmaceutique as the manufacturer.*

FDA Label Image

Pdp1 (Kortribion Box Label 80)

Packaging label for KORTRIBION Pain Reliever tablets, film coated, containing acetaminophen 500 mg and caffeine 65 mg per caplet. The label is bilingual English and Spanish, highlighting pain relief for joint pain, headache, muscle aches, back ache, inflammation, and arthritis. It includes 20 sachets of 4 caplets, distributed by OPMX LLC and made for Inovx Farmaceutique.*

FDA Label Image

Pdp2 (Kortribion Exh 20 4 W80 Caplets (en Es) Rte Rev 06.2026 001 Copia)

KORTRIBION Pain Reliever 500 mg Acetaminophen and 65 mg Caffeine film-coated tablets carton blister pack. The label features the product name in bold red letters on a blue and yellow background with a red upper section. The panel includes drug facts listing active ingredients per caplet as Acetaminophen 500 mg and Caffeine 65 mg, with usage directions and dosage guidelines. The pack contains 4 caplets and is labeled by OPMX LLC.*

* 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.