Label: ANTI-BACTERIAL WASH WITH EXFOLIATING BEADS FOR BLEMISH SKIN- benzoyl peroxide gel
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Contains inactivated NDC Code(s)
NDC Code(s): 62742-4058-1 - Packager: Allure Labs, Inc.
- Category: HUMAN OTC DRUG LABEL
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.
Drug Label Information
Updated September 15, 2010
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- ACTIVE INGREDIENT
- PURPOSE
- WARNINGS
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
INACTIVE INGREDIENTS:
(INCI) Water (Aqua), Cocoamidopropyl Hydroxsultaine, Polyethylene beads, Sodium Lauryl Ether Sulfate, Glycerin, Carbomer, Phenoxyethanol, Caprylyl Glycol, Ethylhexylglycerin, Hexylene Glycol, Aloe barbedensis Leaf Extract, Triethanolamine, Mentha viridis (Spearmint) leaf oil, Melaleuca alternifolia leaf oil, Allantoin, Disodium EDTA, Chamomilla recutita flower extract, Rosemarinus officinalis leaf extract, Eucalyptus globulus leaf oil.
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DEVELOPED BY: DR. KANODIA . DR. KIST
RESEARCH GROUP
www.ayru-medic.com
DISTRIBUTED BY: AESTHETIC INTERNATIONAL
WESTLAKE VILLAGE, CA 91361
MADE IN THE U.S.A
CMSBella
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Vjal ix-Xarolla
Zurrieq Malta ZRQ 1611
IMAGE OF THE LABEL:
AYUR.MEDIC
ANTI-BACTERIAL WASH WITH EXFOLIATING BEADS FOR Blemish Skin
8 fl. oz. (236ml)
- INDICATIONS & USAGE
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INGREDIENTS AND APPEARANCE
ANTI-BACTERIAL WASH WITH EXFOLIATING BEADS FOR BLEMISH SKIN
benzoyl peroxide gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62742-4058 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE 25 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62742-4058-1 236 mL in 1 BOTTLE, PUMP Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333D 01/01/2010 Labeler - Allure Labs, Inc. (926831603)