DOVE- soothing moisture damage therapy anti-dandruff conditioner liquid

Drug Labeling and Warnings

Drug Details [pdf]

DESCRIPTION

Dove Soothing Moisture Damage Therapy Anti-Dandruff Conditioner

ACTIVE INGREDIENT

Pyrithione Zinc 0.5%

PURPOSE

Anti-dandruff

INDICATIONS & USAGE

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

WARNINGS

For external use only.

When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if condition worsens or does not improve after regular use of this product.
If swallowed, get medical help or contact a Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN

Keep this and all drugs out of reach of children.

DOSAGE & ADMINISTRATION

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

INACTIVE INGREDIENT

Water(Aqua), Cetearyl Alcohol, Cyclopentasiloxane, Stearamidopropyl Dimethylamine, Dimethiconol, Behentrimonium Chloride, Fragrance (Parfum), Lactic Acid, Dipropylene Glycol, 1,2-Hexanediol, Benzyl Alcohol, Zinc Sulfate, TEA-Dodecylbenzenesulfonate, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Sodium Chloride.

QUESTIONS

Call 1-800-761-DOVE (3683) or visit us at www.dove.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DOVE 
soothing moisture damage therapy anti-dandruff conditioner liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64942-2447
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
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)
DIMETHICONOL (40 CST) (UNII: 343C7U75XW)
WATER (UNII: 059QF0KO0R)
CYCLOPENTASILOXANE (UNII: 0THT5PCI0R)
ZINC SULFATE (UNII: 89DS0H96TB)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
BENZYL ALCOHOL (UNII: LKG8494WBH)
TEA-DODECYLBENZENESULFONATE (UNII: 8HM7ZD48HN)
ISOSTEARAMIDOPROPYL DIMETHYLAMINE (UNII: P1IO9HNJ3V)
LACTIC ACID (UNII: 33X04XA5AT)
PRUNUS AMYGDALUS DULCIS (SWEET ALMOND) OIL (UNII: 66YXD4DKO9)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64942-2447-1	355 mL in 1 CONTAINER; Type 0: Not a Combination Product	04/08/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	04/08/2026

Labeler - Conopco d/b/a Unilever (001375088)