Oculus Innovative Sciences Announces FDA 510(k) Clearance for Microcyn-Based SebDerm Gel

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Oculus Innovative Sciences, Inc.
OCLS
today announced that it has received a new 510(k) clearance from the U.S. Food and Drug Administration (FDA) for the company's new Microcyn®-based SebDerm Gel.  As a prescription product, SebDerm Gel is intended to manage and relieve the burning, itching, erythema, scaling, and pain experienced with seborrhea and seborrheic dermatitis.  It also helps to relieve dry, waxy skin by maintaining a moist wound and skin environment, which is beneficial to the healing process. Zoe Draelos, MD and president of Dermatology Consulting Services in High Point, North Carolina, commented, "Seborrheic dermatitis is a common condition afflicting men and women of all ages that is challenging for dermatologists to treat.  While treatment options exist, recurrence is common and few options exist for disease maintenance.  A new addition to the dermatologist's armamentarium, such as the Microcyn technology, will be welcome." In addition to U.S. commercialization, which is planned for the quarter ending June 30, 2016, via IntraDerm's 19-person direct sales team, Oculus is working
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