Label: ADVANCE TECHNIQUES KEEP CLEAR ANTI-DANDRUFF TREATMENT- pyrithione zinc lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 10096-0220-1 - Packager: Avon Products, 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 June 11, 2010
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INDICATIONS & USAGE
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WARNINGS
Warnings
For external use only. Consult a health care practitioner prior to use on children under 2 years of age.
When using this product
- avoid contact with eyes. If product gets into eyes, rinse thoroughly with water.
- avoid contact with eyes. If product gets into eyes, rinse thoroughly with water.
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Inactive/non-medicinal ingredients:
WATER/EAU
SD ALCOHOL 40-B
PROPYLENE GLYCOL
HYDROLYZED WHEAT PROTEIN
HYDROLYZED WHEAT STARCH
LAGERSTROEMIA INDICA EXTRACT
ACACIA SENEGAL GUM
DIMETHICONE PEG-8 PHOSPHATE
COCAMIDOPROPYL BETAINE
PARFUM/FRAGRANCE
SALICYLIC ACID
XANTHAN GUM
POTASSIUM HYDROXIDE
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER
MENTHOL
PHENOXYETHANOL
DIMETHICONE PEG-8 MEADOWFOAMATE
PROPYLENE GLYCOL ALGINATE
C12-14 PARETH-12
XYMENYNIC ACID
SODIUM POLYNAPHTHALENESULFONATE
ELAEIS GUINEENSIS (PALM) OIL
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ADVANCE TECHNIQUES KEEP CLEAR ANTI-DANDRUFF TREATMENT
pyrithione zinc lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10096-0220 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC 0.15 mL in 150 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SALICYLIC ACID (UNII: O414PZ4LPZ) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) MENTHOL (UNII: L7T10EIP3A) PHENOXYETHANOL (UNII: HIE492ZZ3T) PROPYLENE GLYCOL ALGINATE (UNII: 26CD3J2R0C) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10096-0220-1 150 mL in 1 BOTTLE, WITH APPLICATOR Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358 06/11/2010 Labeler - Avon Products, Inc. (001468693) Establishment Name Address ID/FEI Business Operations Avon Products, Inc. 005149471 manufacture