Flormar Reborn Foundation Sunscreen Broad Spectrum Spf 20 Sf10 Classic Beige
Product Images NDC 61722-203

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 Flormar Reborn Foundation Sunscreen Broad Spectrum Spf 20 Sf10 Classic Beige (NDC 61722-203). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kosan Kozmetik Sanayi Ve Ticaret A.s., 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

Power Fusion 1 (Powerfusion1)

Power Fusion 1 (Powerfusion1)
Flormar REBORN FOUNDATION SUNSCREEN BROAD SPECTRUM SPF 20 SF10 Classic Beige packaging label. The front panel displays the product name, designation as foundation cream sunscreen broad spectrum SPF 20, and net content of 1.0 fl oz (30 ml). The back panel includes active ingredient Octinoxate 5%, warnings for external use only, usage instructions, manufacturer Kosan Kozmetik Sanayi ve Ticaret A.S. in Turkey, and contact information, along with various regulatory and handling symbols.*
FDA Label Image

Power Fusion 2 (Powerfusion2)

Power Fusion 2 (Powerfusion2)
Drug Facts panel for flormar REBORN FOUNDATION SUNSCREEN BROAD SPECTRUM SPF 20 SF10 Classic Beige by Kosan Kozmetik Sanayi ve Ticaret A.S. This panel includes active ingredient Octinoxate 5% as sunscreen, usage instructions, warnings for external use, directions for application, sun protection measures, and detailed inactive ingredients. Additional product details such as manufacturer address, product description, and contact information for adverse event reporting are also included.*

* 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.