None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - Healthy Korean female adults over the age of 19 - Subjects who have signed a consent form voluntarily after being informed sufficiently on the objectives of study and all related contents - Subjects who are healthy without acute and chronic diseases including skin disorders - Subjects who can be observed and traced throughout the entire study period
Exclusion criteria
Exclusion criteria: - Subjects who are pregnant, breastfeeding, or planning a pregnancy - Subjects who have psychiatric disease and infectious skin disease - Subjects who have used an ointment containing steroids for more than 1 month - Subjects who participated in the similar test within the past 6 months - Subjects who have sensitive and hypersensitive skin - Subjects who have abnormal skin findings at the test site, including moles, acne, erythema, or telangiectasia. - Subjects who have used cosmetics or drugs on the test site with same efficacy within the past 3 months - Subjects who have undergone dermatological treatment or procedures (e.g., liposuction, laser treatment, ultrasound lipolysis, or other skin care procedures) on the test site within the past 6 months - Subjects who are employees of the Sponsor - Subjects deemed by the principal investigator to be unsuitable for participation in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluation of long-lasting UV protection effect | — |
Secondary
| Measure | Time frame |
|---|---|
| Efficacy self report questionnaire;Assessment of skin Adverse Event(AE) | — |
Countries
Korea, Republic of
Contacts
Human Co., Ltd. Skin Clinical Trial Center