Your Name Mineral Sheertint Broad Spectrum Spf 20-almond
Product Images NDC 59735-175

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-almond (NDC 59735-175). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mana Product, 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.

Product Images & Figures Index

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 including active ingredients titanium dioxide 5.0% and zinc oxide 5.0% as sunscreens. It lists purpose, use, warnings, directions, inactive ingredients, and other information such as protection from excessive heat and direct sun. The label is printed on white stock with black text and includes manufacturing and routing information.*
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)
Packaging label template for YOUR NAME Mineral Sheer Tint Broad Spectrum SPF 20 tube by Mana Product, Inc. The label shows front and back panels designed for a white tube with approximate dimensions 76.5 mm by 105 mm. The front panel includes product name, SPF strength, volume (1 fl. oz./30 ml), and icons for recyclable packaging, Made in USA, and 12-month shelf life after opening. The color black is specified for printing.*

* 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.