Inclusion Criteria | Non-Inclusion Criteria |
Specific Sex: female and male; Age: between 30 and 65 years old; Phototype: I to II; Type: Caucasian; Subjects with dry, normal and combination skin. General Healthy subject; Subject having given his/her free informed, written consent; • Subject willing to adhere to the protocol and study procedures. | Female Specific-pregnant or nursing women or women planning to get pregnant during the study; Cutaneous pathology on the study zone (eczema, etc.); Subject with make-up on the day of the visit at the laboratory; Use of topical or systemic treatment during the previous weeks liable to interfere with the assessment of the cutaneous acceptability/efficacy of the study product: - Change in anti-wrinkle, smoothing, firming and/or brightening topical products within previous week on the studied zones, - Non-invasive procedures within previous month on the studied zones, - Intake of food supplement acting on skin within the three previous months, - Invasive procedures: ○ deep chemical peeling within previous 3 months on the studied zones, ○ mesotherapy, dermapen, laser within previous 6 months on the studied zones, ○ botox and/or hyaluronic acid injections within previous 12 months on the studied zones; Subject having undergone a surgery under general anesthesia within the previous month; Excessive exposure to sunlight or UV-rays within the previous month; Subject enrolled in another clinical trial during the study period (concerns the studied zone). |