Acnegenicity Outline: Acnegencity Objective: To determine acnegenic potential of a test material. Subjects: 30 qualified subjects who are prone to break outs with mild-moderate acne Timing: 6-week study Draft report issued within 3 weeks after study completion Product: 35 individual containers with enough product to last for 6 weeks. Label with use instructions only. Methodology: Lesion counts and identification by a Board-Certified Dermatologist Procedures: A Board-Certified Dermatologist qualifies each subject before enrollment by lesion counting and identification. Those qualified are given the product, use instructions and a daily diary to record the date and time of usage. After 3 and 6 weeks of use, subjects return for follow-up evaluations by the Dermatologist. Results are statistically analyzed to determine any differences from baseline.