Young Clariti Mineral Brightening Sheer Tint Broadspectrum Spf 20
Product Images NDC 59735-851

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Young Clariti Mineral Brightening Sheer Tint Broadspectrum Spf 20 (NDC 59735-851). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mana Products , 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

Pdp (Mineral Brightning Sheer Tint Natural Glow)

Pdp (Mineral Brightning Sheer Tint   Natural Glow)
YOUNG CLARITI MINERAL BRIGHTENING SHEER TINT BROADSPECTRUM SPF 20 in a white tube with a black cap. The label states it is a lightweight, mineral-enriched, tinted cream that evens skin tone with a sheer natural radiance, nourishes, moisturizes, and protects. Shade is Natural Glow with a glowing finish. The product size is 1 fl oz (30 ml). Distributed by BIO-UTH Inc., Dover, DE, and made in the USA.*
FDA Label Image

Label-carton (Young Clariti Box Mineral Brightening Sheer Tint Natural Glow 06292022 V1 Print (1) (1) (1))

Label-carton (Young Clariti Box Mineral Brightening Sheer Tint Natural Glow 06292022 V1 Print (1) (1) (1))
Packaging label for YOUNG CLARITI MINERAL BRIGHTENING SHEER TINT BROADSPECTRUM SPF 20 by MANA Products, Inc. The label includes branding and product name, an area showing the tinted moisturizer shade labeled as "Natural Glow Glowing Finish" in a 1 fl oz (30 ml) size. Text covers drug facts, active ingredients (Titanium Dioxide 5.1%, Zinc Oxide 5.0%), warnings, directions, key ingredients, and usage instructions. The design uses a gradient background with purple and white hues, accented by embossing and silver foil as indicated in the color spec chart.*

* 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.