Label: DOVE CLINICAL PROTECTION VISIBLY SMOOTH WILD ROSE ANTIPERSPIRANT AND DEODORANT- aluminum zirconium tetrachlorohydrex gly stick

  • 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 January 31, 2012

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

  • ACTIVE INGREDIENT

    Active Ingredient

    Aluminum Zirconium Tetrachlorohydrex GLY (20%)

  • PURPOSE

    Purpose
    anti-perspirant
  • INDICATIONS & USAGE

    Uses
    ·  reduces underarm wetness
    ·  24 hour protection
    ·  extra effective
  • WARNINGS

    Warnings
    For external use only

    Do not use on broken skin

    Ask a doctor before use if you have kidney disease

    Stop use if rash or irritation occurs

    Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.
  • DOSAGE & ADMINISTRATION

    Directions
    ·  apply to underarms only
    ·  before bed, apply three clicks of product to each underarm
  • INACTIVE INGREDIENT

    Cyclopentasiloxane, Dimethicone, Paraffin, Microcrystalline Wax, Fragrance (Parfum), Silica, Stearyl Alcohol, Helianthus Annuus  (Sunflower) Seed Oil, Dimethicone Crosspolymer, Nylon-12, Sorbitan Laurate, BHT, Palmatine, Red 40 Lake (CI 16035)
  • QUESTIONS

    Questions?  Call toll-free 1-800-761-DOVE

  • PRINCIPAL DISPLAY PANEL

    1.7 oz PDP
    Dove Clinical Protection Visibly Smooth Wild Rose 1.7 oz PDP
  • PRINCIPAL DISPLAY PANEL

    1.7 oz carton
    Dove Clinical Protection Visibly Smooth Wild Rose 1.7 oz Carton PDP
  • INGREDIENTS AND APPEARANCE
    DOVE CLINICAL PROTECTION VISIBLY SMOOTH WILD ROSE  ANTIPERSPIRANT AND DEODORANT
    aluminum zirconium tetrachlorohydrex gly stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1074
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Aluminum Zirconium Tetrachlorohydrex GLY (UNII: 8O386558JE) (Aluminum cation - UNII:3XHB1D032B) Aluminum Zirconium Tetrachlorohydrex GLY20 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    PALMATINE (UNII: G50C034217)  
    SORBITAN MONOLAURATE (UNII: 6W9PS8B71J)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-1074-21 in 1 CARTON
    1NDC:64942-1074-148 g in 1 CONTAINER
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35001/01/2010
    Labeler - Conopco Inc. d/b/a Unilever (001375088)