Compare the Tolerance of Clindamycin 1% /Benzoyl Peroxide (BPO) 5% Gel to Clindamycin 1.2%/ BPO 2.5% Topical Medications

Exclusion Criteria

• •Female subjects who are pregnant, trying to become pregnant, or breast feeding.
• •Male subjects that have facial beards (mustache and/or goatee is acceptable).
• •Is a Type I diabetic.
• •Has active or chronic skin allergies.
• •Has a history of acute or chronic disease that might interfere with, or increase the risk of study participation.
• •Has participated in other facial studies in the preceding 30 days or other clinical studies in preceding 14 days.
• •Had skin cancer treatment in preceding 12 months.
• •Has damaged skin on facial areas (eg, from sunburn, tattoos, scars).
• •Had any medical procedure (eg, laser resurfacing, chemical peels, plastic surgery) to facial areas in preceding 12 months.
• •Had any cosmetic procedure (eg, microdermabrasion, etc.) to facial areas within 8 weeks of the baseline visit.
• •Use of topical retinoids or related agents for the treatment of acne or photoaging in the preceding 6 months.
• •Any dermatological disorder, which in the investigator's opinion, may interfere with the accurate evaluation of the subject's facial appearance.
• •Has known sensitivities or allergies to cosmetics, soaps, fragrances, or any of the ingredients in the test products.
• •Is currently going through menopause and experiencing hot flashes.
• •Received any investigational drug within 30 days of study day 0 or who are scheduled to receive an investigational drug other than the study product during the study.
• •Currently using any medication, which in the opinion of the investigator may affect the evaluation of the study product or place the subject at undue risk (including but not limited to asthma medications, oral steroids, rifampin, anticonvulsants, St. John's wart).
• •Currently taking any topical or oral erythromycin-containing products.
• •History of regional enteritis, ulcerative colitis, or antibiotic-associated colitis.
• •Currently suffering from any disease or condition, which in the opinion of the investigator may affect the evaluation of the study product or place the subject at undue risk.
• •Live in the same household as currently enrolled subjects.
• •Employees of investigator/ clinical research organization (CRO) or Stiefel, a GSK Company involved in the study, or an immediate family member (partner, offspring, parents, siblings or sibling's offspring) of an employee involved in the study.
• •Any other condition or factor the investigator or his duly assigned representative believes may affect the skin response or the interpretation of the test results.