CLINICAL SAFETY STUDIES

NON-COMEDOGENICITY / NON-ACNEGENICITY
Title Objective Schedule Methodology Non-comedogenicity / Non-acnegenicity test under dermatological control. To check the non-comedogenicity / non-acnegenicity and confirm the skin acceptability of a product after repeated application under normal conditions of use.

Optional: To assess subjectively its cosmetic qualities and efficacy.

Duration of the study: 28 days minimum. Beginning: 2 weeks upon receipt of the samples. Report: 3 weeks after the end of the study. Counting of the acne retentional (comedones) and /or inflammatory elements and clinical assessment of the cutaneous response. Skin examination of application site. Counting of the comedones / acne elements on the forehead and cheeks/whole face. Use of the product at home by the subjects for 28 days following the instructions for use. Skin examination and counting of the comedones / acne elements by the investigator/ technician trained under investigator supervision (checking the non-comedogenicity/ non-acnegenicity and acceptability).

ACCEPTABILITY TESTS

Procedure

Optional: - Cosmetic qualities and efficacy questionnaire - Professional pictures - Statistical analysis of the data