None listed
Conditions
Interventions
Intervention1: Test product: FDSS1: Quantity 2 mg/sq.cm Route of administration: Topical Frequency: Once Duration: 24 hour
Control Intervention1: Reference Sunscreen: Quantity 2 mg/sq.cm Route of admi
Sponsors
Foxtale Consumer Pvt Ltd.
Eligibility
Inclusion criteria
Inclusion criteria: 1. Age 18-70 years. 2. Individual should have ITA angle in the range of 28 t0 40, 41 to 55, and greater than 56 3. Individuals free of any dermatological or systemic disorder which would interfere with the results, at the discretion of the investigator. 4. Individuals who have completed a preliminary medical history evaluation. 5. Individuals who have read, understood and signed an informed consent document relating to the specific study to which they are subscribing. 6. Individuals with no known abnormal response to sunlight.
Exclusion criteria
Exclusion criteria: 1.Individuals taking medication which in the opinion of the investigator would mask or interfere with the results. 2.Individuals with chronic skin allergies. 3.Individuals with suntan or sunburn. 4.Individuals with abnormal reaction to the sun. 5.Pregnant or lactating females. 6.Subjects accustomed to using sun beds. 7.Subjects who have participated in an SPF study within the last two months.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in Individual MED (iMED) scoreTimepoint: Day2 | — |
Secondary
| Measure | Time frame |
|---|---|
| Change in Delayed ErythemaTimepoint: Day 3 | — |
Countries
India
Contacts
Public ContactPuneet Mittal
CCFT Laboratories
Outcome results
None listed