Ultra Violette Velvet Screen Blurring Mineral Skinscreen Cream
Product Images NDC 30807-1060

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ultra Violette Velvet Screen Blurring Mineral Skinscreen (NDC 30807-1060). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Wild Child Laboratories Pty Ltd, 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

1 (Velvet Screen 15ml Carton)

ULTRA VIOLETTE Velvet Screen SPF 50 Blurring Mineral Skinscreen cream in 15 mL (0.5 fl. oz.) packaging. Broad Spectrum SPF 50 sunscreen with PA++++ rating, featuring a super-soothing, softly mattifying skin filter. Label indicates active ingredient zinc oxide 22.75 g/100 mL. Manufactured by Wild Child Laboratories PTY Ltd. Includes drug facts, usage directions, warnings, inactive ingredients, and a barcode.*

FDA Label Image

2 (Velvet Screen 50ml Carton)

Packaging label for ULTRA VIOLETTE VELVET SCREEN Blurring Mineral Skinscreen SPF 50 cream, 50 mL (1.7 fl oz), sunscreen with 22.75 g/100 mL Zinc Oxide active ingredient. The label describes it as a broad spectrum, super-soothing, mattifying skin filter suitable for oily, acne-prone, and reactive skin. Distributed by Grace and Fire USA Inc. and made by Wild Child Laboratories PTY Ltd in Australia.*

* 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.