Carte Blanche Multi-hyphenate Brightening Skin Tint Mineral Spf 35 02 Lotion
Product Images NDC 87894-002

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Carte Blanche Multi-hyphenate Brightening Skin Tint Mineral Spf 35 02 (NDC 87894-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Carte Blanche Beauty, 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

Inner Package2 (Inner Package2)

Carte Blanche Multi-Hyphenate Brightening Skin Tint Mineral SPF 35 02 lotion packaging label. The label shows front and back views of a 1 fl. oz (30 ml) bottle. The active ingredient is Zinc Oxide at 13%. The product is a broad spectrum tinted sunscreen distributed by Carte Blanche Beauty, Inc., Los Angeles, CA.*

FDA Label Image

Outer Package2 (Outer Package2)

Drug Facts and product information for Carte Blanche Multi-Hyphenate Brightening Skin Tint Mineral SPF 35 02 lotion. Contains Zinc Oxide 13% as the active ingredient for sunscreen purpose. Includes directions for use, warnings, sun protection measures, inactive ingredients, and marketing text about the product's brightening and skincare benefits. Also covers claims on Vitamin C, Licorice Exosomes, Tomato Extract, and Sheer Zinc Oxide as ingredients contributing to skin tone and protection.*

FDA Label Image

Shade2 (Shade2)

UPC label for Carte Blanche Multi-Hyphenate Brightening Skin Tint Mineral SPF 35 02, featuring a barcode and batch/expiration placeholders. The label includes the number '02' prominently displayed inside a circle and a rectangle, with lot number and expiration fields marked as 'XXXXXX' and 'MM/YYYY' respectively.*

* 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.