Ultra Relief Gel
Product Images NDC 49283-578

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Ultra Relief (NDC 49283-578). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Chemco Corporation, 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

Ultra Relief Gel (Ultra Relief Menthol 6 Camphor 3)

Drug Facts panel for ULTRA RELIEF topical gel containing 6% Menthol and 3% Camphor as active ingredients. It provides details on use as a topical analgesic for minor muscle or joint pain, warnings for external use only, instructions for use, and precautions including avoiding use on large or damaged skin areas. Directions specify application for adults and children over 12 years, with guidance for storage and a full list of inactive ingredients.*

* 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.