Label: DOVE MEN PLUS CARE ANTI DANDRUFF- pyrithione zinc shampoo 

  • Label RSS
  • NDC Code(s): 64942-1273-1, 64942-1273-2, 64942-1273-3, 64942-1273-4
  • Packager: Conopco Inc. d/b/a Unilever
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 08/13

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    ACTIVE INGREDIENT

    Pyrithione Zinc (1.0%)

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  • PURPOSE

    PURPOSE

    Antidandruff

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  • INDICATIONS & USAGE

    USE: helps prevent and control recurrence of itching and flaking associated with dandruff

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  • WARNINGS

    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.

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

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  • DOSAGE & ADMINISTRATION

    DIRECTIONS: Wet hair, massage into scalp, rinse. Repeat if desired. For best results use at least twice a week or as directed by a doctor.

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  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS:Water (Aqua), Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Fragrance (Parfum), Carbomer, Dimethiconol, DMDM Hydantoin, Citric Acid, Guar Hydroxypropyltrimonium Chloride, TEA-Dodecylbenzenesulfonate, Butylene Glycol, Iodopropynyl Butylcarbamate, Caffiene, PPG-9, Methylchloroisothiazolinone, Methylisothiazolinone

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  • QUESTIONS

    Questions, comments?: Call 1-800-761-DOVE(3683) or visit us at www.dove.com

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  • PDP 25.4 FL. OZ.
  • INGREDIENTS AND APPEARANCE
    DOVE  MEN PLUS CARE ANTI DANDRUFF
    pyrithione zinc shampoo
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:64942-1273
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Pyrithione Zinc (Pyrithione Zinc) Pyrithione Zinc 1.0 g  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    SODIUM LAURETH SULFATE  
    COCAMIDOPROPYL BETAINE  
    SODIUM CHLORIDE  
    DMDM HYDANTOIN  
    TRIETHANOLAMINE DODECYLBENZENESULFONATE  
    CITRIC ACID MONOHYDRATE  
    PPG-9  
    METHYLCHLOROISOTHIAZOLINONE  
    METHYLISOTHIAZOLINONE  
    GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE)  
    DIMETHICONOL (41 MPA.S)  
    CAFFEINE  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:64942-1273-1 750 mL in 1 CONTAINER
    2 NDC:64942-1273-2 355 mL in 1 CONTAINER
    3 NDC:64942-1273-3 950 mL in 1 CONTAINER
    4 NDC:64942-1273-4 89 mL in 1 CONTAINER
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part358H 01/01/2013
    Labeler - Conopco Inc. d/b/a Unilever (001375088)
    Establishment
    Name Address ID/FEI Business Operations
    Alberto-Culver USA Inc. 021679448 manufacture(64942-1273)
    Establishment
    Name Address ID/FEI Business Operations
    Unilever Supply Chain Co. d/b/a Unilever 043510056 manufacture(64942-1273)
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