Your Name Mineral Sheertint Broad Spectrum Spf 20-light Cream
Product Images NDC 59735-177

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Your Name Mineral Sheertint Broad Spectrum Spf 20-light (NDC 59735-177). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pml Nyc, Llc, 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 (Man 220 Bfs 0000d Mineral Sheer Tint Spf 20 (insert) Page 0001 (1))

Pdp (Man 220 Bfs 0000d   Mineral Sheer Tint Spf 20 (insert) Page 0001 (1))
Drug Facts panel for YOUR NAME MINERAL SHEER TINT BROAD SPECTRUM SPF 20 lists active ingredients Titanium Dioxide 5.0% and Zinc Oxide 5.0% as sunscreens. It includes use information to help prevent sunburn, warnings for external use only, directions for application before sun exposure, and inactive ingredients such as water and various extracts. Other information advises protection from heat and sun.*
FDA Label Image

Pdp (Man 240 Jal Bfsb Mineral Sheer Tint (screen) Page 0001)

Pdp (Man 240 Jal Bfsb  Mineral Sheer Tint (screen) Page 0001)
Label template for YOUR NAME MINERAL SHEER TINT BROAD SPECTRUM SPF 20 in a white 1 fl. oz. (30 ml) tube. The front panel displays the product name, broad spectrum SPF 20 designation, and volume. The label notes the product as a lightweight, mineral-based foundation with a sheer, natural finish. Manufacturer is Mana Product, Inc. The label also includes standard packaging icons such as a 12-month expiration after opening symbol and a Made in U.S.A. mark.*

* 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.