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)

This is a drug facts label for a product called "ULTRA RELIEF" with active ingredients Menthol 6% and Camphor 3%. It is intended for temporary relief of minor pain in muscles or joints. The product should be used externally only and users should avoid applying it on large areas of the body or damaged skin. Directions for use include applying a small amount to the affected area, massaging in a circular motion, and repeating up to 3 to 4 times daily. The product should be stored in a dry place at room temperature. It contains various inactive ingredients like peppermint oil, tea tree leaf oil, and thyme oil.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.