DOVE- pyrithione zinc liquid

Dove by

Drug Labeling and Warnings

Dove by is a Otc medication manufactured, distributed, or labeled by Conopco, Inc. d/b/a/ Unilever. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOVE DERMACARE SCALP ALOE & RESTORE ANTI-DANDRUFF CONDITIONER - pyrithione zinc liquid

Dove Dermacare Scalp Aloe & Restore Anti-Dandruff Conditioner

Drug Facts

Active ingredient
Pyrithione Zinc (0.5%)

Purpose

Anti-dandruff

Use

Helps prevent and control recurrence of itching, flaking and irritation associated with dandruff.

Warning

For external use only
When using this product: Avoid contact with eyes. If contact occurs, rinse eyes thoroughtly with water.
Stop use and ask a doctor if: Condition worsens or does not improve after regular use of this product as directed.

KEEP OUT OF REACH OF CHILDREN

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

Directions

For best results use at least twice per week or as directed by a doctor. Massage into scalp and hair. Rinse.

Inactive Ingredients

Water(Aqua), Cetearyl Alcohol, Cyclopentasiloxne, Stearamidopropyl Dimethylamine, Dimethiconol, Behentrimonium Chloride, Aloe Barbadensis Leaf Juice, Zingiber Zerumbet Extract, Tocopheryl Acetate, Panthenol, Fragrance(Parfum), Dipropylene Glycol, Lactic Acid, DMDM Hydantoin, Zinc Sulfate, Sodium Chloride, TEA-Dodecylbenzenesulfonate, Butylene Glycol, Iodopropynyl Butylcarbamate, PEG-150 Distearate.

Questions?

Call 1-800-761-3683

Packaging

INGREDIENTS AND APPEARANCE

DOVE 
pyrithione zinc liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64942-1620
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5)	PYRITHIONE ZINC	0.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
STEARAMIDOPROPYL DIMETHYLAMINE (UNII: K7VEI00UFR)
DIMETHICONOL (40 CST) (UNII: 343C7U75XW)
BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)
DMDM HYDANTOIN (UNII: BYR0546TOW)
ZINC SULFATE, UNSPECIFIED FORM (UNII: 89DS0H96TB)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
TRIETHANOLAMINE DODECYLBENZENESULFONATE (UNII: 8HM7ZD48HN)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
PANTHENOL (UNII: WV9CM0O67Z)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64942-1620-1	355 mL in 1 CONTAINER; Type 0: Not a Combination Product	10/12/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358H	10/12/2018

Labeler - Conopco, Inc. d/b/a/ Unilever (001375088)