Visit 1: Potential panelists will report to the Testing Facility at their scheduled appointment time without having applied any face or eye makeup and complete an ICF to become subjects. All panelists will undergo an external visual gynecological exam by a Board-Certified Gynecologist for evidence of any vulvar or perineal redness, swelling, inflammation or irritation. Panelists presenting a score of 2 or more for any parameter will not qualify. Panelists will then be screened by a Board-Certified Ophthalmologist. The Ophthalmologist will evaluate each panelists' eyes in addition to measuring vision. Qualified panelists will be provided with a 4-week supply of the test material and a daily diary to document use. Written and verbal instructions for use, supplied by the will be provided for each panelist. Panelists will be instructed not to introduce any new cosmetic, toiletry, or personal care products during the trial. To document compliance, panelist will be required to maintain a daily diary of test material use.
Visit 2: After using the test material for 4 weeks, panelists will report to the Testing Facility at their scheduled appointment time without having applied any face or eye makeup. Any unused test material and daily diaries will be returned to the Testing Facility. Panelists will be given a questionnaire to complete. A final examination and evaluation will be conducted by a Board-Certified Gynecologist and Board Certified Ophthalmologist, as previously described.
***Exclusive– No other studies***
*must have self-perceived sensitive skin***