Label: CLEAR CELL CLEANSER- salicylic acid gel
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Contains inactivated NDC Code(s)
NDC Code(s): 62742-4045-1 - Packager: Allure Labs, Inc.
- 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.
Drug Label Information
Updated July 28, 2010
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INDICATIONS & USAGE
INDICATIONS AND USAGE SECTION:
A daily Salicylic acid cleanser that exfoiates, gently removes makeup and diminishes excess oil. Anti-oxidants keep skin soft, purified and shine-free.
Paraben free
DIRECTIONS:
Apply to wet face and massage for 1 minute. Repeat cleansing for additional exfoliation.
INDICATIONS:
Acne and acne-prone skin
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
INACTIVE INGREDIENTS:
Water (Aqua), Ammonium Laureth Sulfate, Disodium cocoamphodiacetate, Glycerin, PEG 120 Methyl Glucose Dioleate, Phenoxyethanol, Caprylyl Glycol, Camellia sinensis (Green Tea) leaf extract, Ethylhexylglycerin, Polyquaternium-10, Hexylene Glycol, Arnica montana (Arnica) flower extract, Chamomilla recutita (Chamomile) flower extract, Aesculus hippocastanum (Horse Chestnut) extract, Melia azadirachta (neem) leaft extract, Hamamelis virginiana (Witch Hazel) water, Melaleuca alternifolia (Tea Tree) leaf oil, Mentha viridis (spearmint) oil, Eucalyptus globulus (Eucalyptus) leaf oil.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CLEAR CELL CLEANSER
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62742-4045 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 30 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62742-4045-1 177.6 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)