Ultra Glow Fade
Product Images NDC 58318-008

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Ultra Glow Fade (NDC 58318-008). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Keystone Laboratories, 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

Label (Ug Fade Creaml)

This text seems to be related to a product label. It includes information about the product's inactive ingredients, such as alcohol, isopropyl, paraben, citric acid, among others. The product is called Ultra Glow and it is a fade cream with skin lightener properties, containing 9% Hydroquinone and 1.5% Padimate O Sunscreen. The label contains important information such as the job information, size, and color of the label. It also includes a note on legal compliance and the responsibility of the user to comply with all laws and regulations. There is a section to approve the artwork and make changes if necessary.*

* 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.