Label: CLEARSKIN PORE PENETRATING CLEANSER- triclosan gel
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Contains inactivated NDC Code(s)
NDC Code(s): 10096-0199-1 - Packager: Avon Products, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 June 2, 2010
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Inactive Ingredients
WATER/EAU
SODIUM LAURETH SULFATE
GLYCERIN
DISODIUM LAURETH SULFOSUCCINATE
COCAMIDOPROPYL HYDROXYSULTAINE
PROPYLENE GLYCOL
HAMAMELIS VIRGINIANA (WITCH HAZEL) EXTRACT
EUCALYPTUS GLOBULUS LEAF EXTRACT
LAURAMIDOPROPYL BETAINE
PPG-12-BUTETH-16
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER
HYDROXYPROPYL METHYLCELLULOSE
LACTOSE
CELLULOSE
BENZOPHENONE-4
POTASSIUM HYDROXIDE
METHYLPARABEN
DISODIUM EDTA
PHOSPHORIC ACID
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
PARFUM/FRAGRANCE
CHROMIUM HYDROXIDE GREEN/CI 77289
YELLOW 6/CI 15985
YELLOW 10/CI 47005
BLUE 1/CI 42090
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CLEARSKIN PORE PENETRATING CLEANSER
triclosan gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10096-0199 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN 0.5 mL in 125 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) GLYCERIN (UNII: PDC6A3C0OX) DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233) LACTOSE (UNII: J2B2A4N98G) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) METHYLPARABEN (UNII: A2I8C7HI9T) PHOSPHORIC ACID (UNII: E4GA8884NN) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10096-0199-1 125 mL in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333 06/02/2010 Labeler - Avon Products, Inc. (001468693) Establishment Name Address ID/FEI Business Operations Avon Products, Inc. 005149471 manufacture