Label: DOVE- pyrithione zinc liquid

  • NDC Code(s): 64942-1621-1
  • Packager: Conopco, Inc. d/b/a/ Unilever
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated December 7, 2022

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  • DOVE MEN+CARE DERMACARE SCALP DEEP CLEAN ANTI-DANDRUFF SHAMPOO + CONDITIONER - pyrithione zinc liquid

    Dove Men+Care Dermacare Scalp Deep Clean Anti-Dandruff Shampoo + Conditioner

  • Drug Facts

    Active ingredient
    Pyrithione Zinc (1.0%)

  • Purpose

    Anti-dandruff

  • Use

    • 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 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), Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Fragrance (Parfum), Carbomer, Dimethiconol, DMDM Hydantoin, Citric Acid, Zinc Sulfate, PPG-9, Guar Hydroxypropyltrimonium Chloride, TEA-Dodecylbenzenesulfonate, Melaleuca Alternifolia (Tea Tree) Leaf Extract, Butylene Glycol, Iodopropynyl Butylcarbamate, Methylchloroisothiazolinone, Methylisothiazolinone.

  • Questions, comments?

    Call 1-800-761-3683

  • Packaging

    DoveDeepCleanAntiDandruffSHCD

  • INGREDIENTS AND APPEARANCE
    DOVE 
    pyrithione zinc liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1621
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    LAURETH-23 (UNII: N72LMW566G)  
    ALMOND OIL (UNII: 66YXD4DKO9)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    DIMETHICONOL (40 CST) (UNII: 343C7U75XW)  
    CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    ZINC SULFATE, UNSPECIFIED FORM (UNII: 89DS0H96TB)  
    TRIETHANOLAMINE DODECYLBENZENESULFONATE (UNII: 8HM7ZD48HN)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    PPG-9 (UNII: I29VQH0G0B)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    POLOXAMER 407 (UNII: TUF2IVW3M2)  
    LAURETH-4 (UNII: 6HQ855798J)  
    POLYETHYLENE GLYCOL 200 (UNII: R95B8J264J)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    SOYBEAN OIL (UNII: 241ATL177A)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    SPEARMINT OIL (UNII: C3M81465G5)  
    ASIAN GINSENG (UNII: CUQ3A77YXI)  
    MENTHOL (UNII: L7T10EIP3A)  
    LYSINE HYDROCHLORIDE (UNII: JNJ23Q2COM)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-1621-1355 mL in 1 CONTAINER; Type 0: Not a Combination Product01/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart358H01/01/2020
    Labeler - Conopco, Inc. d/b/a/ Unilever (001375088)
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