Flormar Reborn Foundation Sunscreen Broad Spectrum Spf 20 Sf04 Rich Beige
Product Images NDC 61722-201

2 FDA label images from Kosan Kozmetik Sanayi Ve Ticaret A.s. · 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 Sf04 Rich Beige (NDC 61722-201). 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.

Product Images & Figures Index

FDA Label Image

Power Fusion 1 (Powerfusion1)

Power Fusion 1 (Powerfusion1)
The image shows the front and back labels of flormar REBORN FOUNDATION SUNSCREEN BROAD SPECTRUM SPF 20 in a 1.0 fl oz (30 ml) cream sunscreen form. The front label includes the product name and volume, while the back label lists the active ingredient Octinoxate 5%, warnings for external use, contact information for Kosan Kozmetik Sanayi ve Ticaret A.S. in Turkey, and usage instructions. The label advises seeing the outer container for complete drug facts and includes a website and phone number for reporting adverse events.*
FDA Label Image

Power Fusion 2 (Powerfusion2)

Power Fusion 2 (Powerfusion2)
Drug Facts panel for flormar REBORN FOUNDATION SUNSCREEN BROAD SPECTRUM SPF 20 SF04 Rich Beige showing active ingredient Octinoxate 5%. Includes uses such as helping to prevent sunburn, warnings about external use only, directions for application, and inactive ingredients. Additional product details include the labeler Kosan Kozmetik Sanayi ve Ticaret A.S., product size 1.0 fl oz (30 ml), and manufacturer location in Turkey.*

* 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.