Bareminerals
Product Images NDC 98132-160

2 FDA label images from Orveon Global Us Llc · 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 Bareminerals (NDC 98132-160). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Orveon Global Us 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

Principal Display Panel (6 g Jar Label (Original))

Principal Display Panel (6 g Jar Label (Original))
Drug Facts panels for bareMinerals Original SPF 25 Mineral Veil 6 g (0.21 oz) list active ingredients Titanium Dioxide 25% and Zinc Oxide 10%, both as sunscreens. Warnings include external use only, avoid eyes, and rinse with water to remove. Directions advise even application before sun exposure. Additional info includes storage instructions and inactive ingredients such as silica, starches, zinc stearate, and magnesium stearate, with possible iron oxides. Manufacturer details are Bare Escentuals Beauty, Inc., San Francisco, CA.*
FDA Label Image

Principal Display Panel (6 g Jar Label (Tinted))

Principal Display Panel (6 g Jar Label (Tinted))
Drug Facts panels for BareMinerals Tinted SPF 25 Mineral Veil 6 g (0.21 oz) show active ingredients titanium dioxide 25% and zinc oxide 10% as sunscreens. The text includes warnings for external use only, directions to apply evenly before sun exposure, storage instructions, and inactive ingredients such as silica and corn starch. Additional warnings advise keeping out of reach of children and eyes, and to stop use if rash or irritation develops.*

* 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.