None listed
Conditions
Interventions
Intervention1: Tan Vanish Gluta Kojic Skin Polish
: Mode of Usage: Use the provided spatula, which has one small spoon and one large spoon. Measure 1 small spoon of Tan Vanish Gluta-Kojic Powder and
Sponsors
Sun Chem India
Eligibility
Inclusion criteria
Inclusion criteria: 1) Age 18 years old or above male and female consumers. 2) Sex Healthy male and non-pregnant/non-lactating female. 3) Females of childbearing potential must have a self-reported negative urine pregnancy test. 4) Subject is in good general health as determined by the Investigator on the basis of medical history. 5) Consumers should be willing and able to follow the study protocol to participate in the study. 6) Subject must be able to understand and provide written Subject s information sheet to participate in the study. 7) Consumers is willing not to use any other marketed product on application site during the study period.
Exclusion criteria
Exclusion criteria: 1) Subject has any known allergy to test product ingredient. 2) Presence of any chronic disease or illness in the past three months or any clinically significant on-going chronic medical illness e.g. Congestive cardiac failure, Hepatitis, Hypotensive episodes, etc. 3) Participation in any similar consumer study within the past 90 days. 4) Currently using any topical medications. 5) Any exceptions to the inclusion/exclusion criteria will be considered on a case-by case basis and will be documented in the case report form
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.To evaluate the effectiveness of the test product by assessing the change in skin colour parameters L, a, b, and ITA from baseline to post-removal of the product. 2.To evaluate the effectiveness of the test product based on consumer perception questionnaire in terms of instant tanning removal in 20 mins, burning, itching, post-removal of the product. 3.To evaluate the effectiveness of the test product by assessing change in visual appearance from baseline to post removal of the test product. 4.To evaluate the effectiveness of the test product by assessing change in skin surface pH from baseline to post removal of the test product. Timepoint: 1.Baseline and at 20 mins post removal 2.Baseline and at 20 mins post removal 3.Baseline and at 20 mins post removal 4.Baseline and at 20 mins post removal | — |
Secondary
| Measure | Time frame |
|---|---|
| NILTimepoint: NA | — |
Countries
India
Contacts
Public ContactMaheshvari Patel
NovoBliss Research Private Limited
Outcome results
None listed