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)

The image shows the front and side label of Suntone After Sun Burn Relief Gel with Lidocaine by Prime Enterprises Inc. The front label highlights the product name, strength, and form as a 16 FL. OZ. (470 mL) gel containing lidocaine and moisturizing aloe vera. The side panel includes Drug Facts detailing active ingredients, uses, warnings, directions, inactive ingredients, and contact information for Biocycle Laboratories, Inc., Miami, FL. The label also displays a barcode and states the product is made in the USA.*

* 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.