Label: CLEAR CELL MEDICATED ACNE SCRUB- benzoyl peroxide cream
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Updated July 1, 2010
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- ACTIVE INGREDIENT
Water, Cocamidopropyl Hydroxysultane, Micro-Exfoliant Beads, Cera Alba (Bees Wax), Ammonium Laureth Sulfate, Glycerin, Aloe Barbadensis (Aloe Vera) Leaf Extract, Melia Azadirachta (Neem) Leaf Extract, Symphytum Officinale (Comfrey) Extract, Carbomer, Triethanolamine, Mentha Virdis (Spearmint) Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Eucalyptus Globulus (Eucalyptus) Leaf Oil, Camellia Sinensis (Green Tea) Leaf Extract, Arnica Montana (Arnica) Flower Extract, Chamomilla Recutita (Chamomile) Flower Extract, Aesculus Hippocastanum (Horse Chestnut) Extract, Allantoin, Disodium EDTA.
PRINCIPAL DISPLAY PANEL
Other Information on the back of the container:
A micro-exfoliating cleanser with benoyl peroxide to treat active acne. A blend of anti-oxidants soothe irritated and red, inflamed lesions leaving skin healthy and blemish free.Distributor:
Apply a liberal amount to wet face and massage for 1 minute. This gentle exfoliation process assists in reducing active acne and thoroughly cleansing oily skin. Rinse with cold water. Use morning and evening. Note: Do not overstimulate active lesions.
Active acne and acne-prone skin.
Palm Beach, FL 33411 USA
Image of the Product:
CLEAR CELL Medicated Acne Scrub:
INGREDIENTS AND APPEARANCE
CLEAR CELL MEDICATED ACNE SCRUB
benzoyl peroxide cream
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62742-4034 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE 30 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62742-4034-1 177.6 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333 01/01/2010 Labeler - Allure Labs, Inc. (926831603)