DOVE- calming relief damage therapy anti-dandruff 2 in 1 shampoo and conditioner liquid

Drug Labeling and Warnings

Drug Details [pdf]

DESCRIPTION

Dove Calming Relief Damage Therapy Anti-Dandruff 2 in 1 Shampoo + Conditioner

ACTIVE INGREDIENT

Pyrithione Zinc 1.0%

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 as directed.
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
into scalp and hair. Rinse.

INACTIVE INGREDIENT

Water (Aqua), Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Carbomer, Fragrance (Parfum), Citric Acid, Dimethiconol, Phenoxyethanol, Sodium Benzoate, Sodium Salicylate, Zinc Sulfate, PPG-9, Guar Hydroxypropyltrimonium Chloride, TEA-Dodecylbenzenesulfonate, Aloe Barbadensis Leaf Juice,
Cocos Nucifera (Coconut) Oil, Butyrospermum Parkii (Shea) Butter.

QUESTIONS

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DOVE 
calming relief damage therapy anti-dandruff 2 in 1 shampoo and conditioner liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64942-2443
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5)	PYRITHIONE ZINC	1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER (UNII: 0A5MM307FC)
WATER (UNII: 059QF0KO0R)
CITRIC ACID (UNII: 2968PHW8QP)
SODIUM BENZOATE (UNII: OJ245FE5EU)
ZINC SULFATE (UNII: 89DS0H96TB)
TEA-DODECYLBENZENESULFONATE (UNII: 8HM7ZD48HN)
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)
BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y)
COCOS NUCIFERA (COCONUT) OIL (UNII: Q9L0O73W7L)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM SALICYLATE (UNII: WIQ1H85SYP)
PPG-9 (UNII: I29VQH0G0B)
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (UNII: B16G315W7A)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
DIMETHICONOL (40 CST) (UNII: 343C7U75XW)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64942-2443-1	532 mL in 1 CONTAINER; Type 0: Not a Combination Product	04/06/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	04/06/2026

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