Ultra Glow Fade
Product Images NDC 58318-002

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Ultra Glow Fade (NDC 58318-002). 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.

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FDA Label Image

Label Image (Ug Fade Spf Label)

Label Image (Ug Fade Spf Label)
This is a description of a skin fade cream with aloe vera for normal skin. The cream helps to reduce discoloration or skin imperfections, and it is advised to apply a small amount twice daily. The desired results are typically visible within two weeks of usage. If no improvement is visible within 90 days of treatment, users should discontinue the use of the product. There are also directions and precautions listed for application, such as conducting a patch test before applying to larger areas. The active ingredients include 2% hydroquinone and 15% padimate 0, while the other ingredients consist of a mix of chemicals and natural substances. There is a caution about discontinuing use if skin irritation occurs, and it is not advised to use the product on children under 12 years of age. The product is made in LS. However, there is additional text in a different language that cannot be translated, and it is not relevant to the description.*

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