The study aims to determine the Sun Protection Factor (SPF) of 8 cosmetic products in vivo on the back of human participants, according to the International Standard Sun Protection Test method by using a sun simulator.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Enrollment
28
Untreated area
High SPF Standard P3/SPF 15
Yosemite Falls (Forte Day SPF upgrade) Variant A
GSK Investigational Site
Schenefeld, Schleswig-Holstein, Germany
Visual evaluation of irradiated skin
Visual evaluation of irradiated test area will be carried out to determine Minimal Erthemal Dose (MED). The lowest irradiation dose producing perceptible erythema will be chosen as MED. The individual SPF (SPFi) for each test product will be determined by calculating the ratio of the MED on test product protected skin (MEDp) to the MED on unprotected skin (MEDu).
Time frame: Upto 2 weeks
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Yosemite Falls (Forte Day SPF upgrade) Variant B
Yosemite Falls (Forte Day SPF upgrade) Variant C
Yosemite Falls (Forte Day SPF upgrade) Variant D
Yosemite Falls (Forte Day SPF upgrade) Variant E
Yosemite Falls (Forte Day SPF upgrade) Variant F
Yosemite Falls (Forte Day SPF upgrade) Variant G
Yosemite Falls (Forte Day SPF upgrade) Variant H