Bareminerals Original Foundation Broad Spectrum Spf 15 Powder
Product Images NDC 98132-023

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Bareminerals Original Foundation Broad Spectrum Spf 15 (NDC 98132-023). 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 (8 g Jar Label)

Label for bareMinerals Original Foundation Broad Spectrum SPF 15 in the shade Fairly Light 03, a topical powder with 2000 mg/8g strength. The label includes Drug Facts with active ingredient titanium dioxide 25% as sunscreen, uses, warnings, directions, other information, and inactive ingredients such as bismuth oxychloride, mica, and iron oxides. The product is distributed by Orveon Global US LLC and made in the USA, with net weight 8 g (0.28 oz).*

FDA Label Image

Principal Display Panel (8 g Jar Label)

Label for bareMinerals Original Foundation Broad Spectrum SPF 15 Medium 10 powder, containing 8 g (0.28 oz) of product. Active ingredient titanium dioxide 25% serves as a sunscreen. The label includes Drug Facts, warnings, directions for sunscreen use, inactive ingredients, and contact information for questions. Labeler is Orveon Global US LLC.*

FDA Label Image

Principal Display Panel (8 g Jar Label)

Packaging label for bareMinerals Original Foundation Broad Spectrum SPF 15 in the shade Golden Medium 14. The product is a topical powder with a net weight of 8 g (0.28 oz). The label includes Drug Facts panels detailing active and inactive ingredients, uses, warnings, directions for use, and manufacturer information for Orveon Global US LLC.*

* 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.