Bioderma Photoderm X-Defense Ultra Fluid Spf50+ Face Sunscreen Invisible 40ml

About this product

The 1st detox ultra-fluid suncare for a global protection against environmental aggressors, sun & pollution. Formulated in an insivible shade suitable for all skintypes and phototypes. Bioderma creates a new exclusive technology, environmental active defense, which provides an overall skin protection against UV rays, visible light, infrared light & pollution. Reduction of -99 % cellular damages face to UV rays, visible light and infrared light (1). In addition, inspired by our unique NAOS ecobiology approach, Photoderm xdefense ultra-fluid spf50+ contains the detox science to strengthen the skin's natural detoxification mechanism and helps the skin to find its own balance face to environmental aggressors. +164% skin detox power for more radiant skin (2)Extremely sensorial: Ultra-fluid - Ultra dry touch - invisible with no white cast - Excellent make-up base - Fragranced - Very good cutaneous and ocular tolerance - Non-comedogenic. Recommended by dermatologists. Virtuous formula: minimalism sunscreen filters and no unnecessary ingredients for the skin ( microplastics and silicones) & Aquatic ecosystems testedPROTECTSAgainst short & long UVA rays, UVB rays, visible light, infrared light, pollution.-99 % cellular damages face to UV rays, visible light and infrared light (1).-33% pollution on the skin (3)DETOX+164% skin detox power* for more radiant skin (2).+43% complexion radiance (4)HYDRATES 8h skin hydration (5)MATIFIES All day matte sensation (6)TEXTURE: VERY PLEASANT TO USE (5)The product is ultra fluid for 100% of users (7)The product leaves an ultra-dry touch finish for 73 % of users (6)The product is invisible on the skin and doesn't leave white marks for 100% of users (7)(1) Ex vivo evaluation of DNA damage by thymine dimers measurement with Photoderm Xdefense ultra-fluid SPF50+ on skin explant exposed to UV, visible light and infra-red light, versus untreated irradiated control, France 2024.(2) In vitro evaluation of gene expression of Metallothionein 1-G wit