ADVANCED SEBORRHEIC DERMATITIS THERAPY- pyrithione zinc soap

ADVANCED SEBORRHEIC DERMATITIS THERAPY by

Drug Labeling and Warnings

ADVANCED SEBORRHEIC DERMATITIS THERAPY by is a Otc medication manufactured, distributed, or labeled by CVS Pharmacy, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Pyrithione Zinc 2%

Purpose

Dandruff/Seborrheic Dermatitis

Use

For relief of skin itching, flaking, and scaling associated with dandruff and seborrheic dermatitis

Warnings

For external use only

KEEP OUT OF REACH OF CHILDREN

• Keep out of the reach of children.
• If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

■ Use on affected areas in place of your regular soap
■ For best results use at least twice a week or as directed by a doctor

When using this product

■ avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if

Stop use and ask a doctor if ■ condition worsens, or does not improve after regular use of this product as directed.

Ask a doctor before use

Ask a doctor before use if you have seborrheic dermatitis that covers a large portion of the body.

INACTIVE INGREDIENT

Sodium Palmate, Sodium Palm Kernelate, Water, Glycerin, Palmitic Acid, Titanium Dioxide (CI 77891), Sodium Chloride, Jojoba Esters, Tetrasodium EDTA, Tetrasodium Etidronate, Iron Oxides (CI 77499), Ferric Ferrocyanide, Green 5 (CI 61570),
Yellow 10 (CI 47005)

Questions?

www.CVS.com

1-800-SHOP CVS

Label

INGREDIENTS AND APPEARANCE

ADVANCED SEBORRHEIC DERMATITIS THERAPY 
pyrithione zinc soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69842-343
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5)	PYRITHIONE ZINC	2 g  in 1000 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)
SODIUM PALMATE (UNII: S0A6004K3Z)
PALMITIC ACID (UNII: 2V16EO95H1)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
ETIDRONATE TETRASODIUM (UNII: CZZ9T1T1X4)
EDETATE SODIUM (UNII: MP1J8420LU)
HYDROGENATED JOJOBA OIL (UNII: 7F674YQ5SO)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
FERRIC FERROCYANIDE (UNII: TLE294X33A)
FERROUS OXIDE (UNII: G7036X8B5H)
D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)

Product Characteristics
Color	green	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69842-343-78	119 g in 1 BOX; Type 0: Not a Combination Product	06/10/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358H	06/10/2016

Labeler - CVS Pharmacy, Inc. (062312574)