Suntone
Product Images NDC 58443-0125

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Suntone (NDC 58443-0125). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Prime Enterprises Inc., 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

Principal Display Image (58443 0125 6)

This is a description of Suntone After Sun Burn Relief Gel that contains Lidocaine Hydrochloride and Aloe Vera to soothe and moisturize skin. It is used for the temporary relief of pain and itching caused by minor skin irritations, scrapes, insect bites, sunburn or minor burns. The product comes with directions for use and warnings against excessive use on blistered areas or raw skin. The inactive ingredients include Aloe Barbadensis Leaf Juice, Benzophenone-4, Blue I, Carbomer, Diazolidiny! Urea, Disodium EDTA, DMDM Hydantoin, Fragrance, Menthol, Methylparaben, Polysorbate-20, Propylene Glycol, Sd Alcohol 40-B, Triethanolamine, Water, Yellow 5. The product is distributed by Biocycle Laboratories, Inc. in Miami, FL.*

* 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.