Drug Facts

Active/medicinal ingredient Purpose

Pyrithione Zinc 0.1%..........................................Antidandruff

Uses

reduces the symptoms of dandruff
controls scalp flaking associated with dandruff

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.

Stop us and ask a health care practitioner if

rash or irritation occurs
condition worsens or does not improve after regular use.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Apply to scalp one to three times daily or as directed by a health care practitioner. After shampooing and conditioning your hair, thoroughly towel-dry. Part hair section by section and apply a few drops to scalp using applicator tip along parts. Do not rinse. Style as usual.

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? Call 1-800-FOR-AVON
or 1-800-265-AVON in Canada

image of label

ADVANCE TECHNIQUES KEEP CLEAR ANTI-DANDRUFF TREATMENT
pyrithione zinc lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:10096-0220
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5)	PYRITHIONE ZINC	0.15 mL in 150 mL

Ingredient Name	Strength
Inactive Ingredients
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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:10096-0220-1	150 mL in 1 BOTTLE, WITH APPLICATOR

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part358	06/11/2010

Labeler - Avon Products, Inc. (001468693)

Name	Address	ID/FEI	Business Operations
Establishment
Avon Products, Inc.		005149471	manufacture