Label: DOVE ULTIMATE GO FRESH BURST 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 May 26, 2011

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

View All Sections
  • ACTIVE INGREDIENT

    Active ingredient

    Aluminum Zirconium Tetrachlorohydrex GLY(14.8%)
  • PURPOSE

    Purpose
    antiperspirant
  • INDICATIONS & USAGE

    Uses
    · reduces underarm wetness
    · 24 Hour Protection
  • 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
  • INACTIVE INGREDIENT

    Cyclopentasiloxane
    Stearyl Alcohol
    C12-15 Alkyl Benzoate
    PPG-14 Butyl Ether
    Hydrogenated Castor Oil
    Fragrance (Parfum)
    Dimethicone
    Polyethylene
    Steareth-100
    Helianthus Annuus (Sunflower) Seed Oil
    BHT
  • QUESTIONS

    Questions?
    Call toll-free 1-800-761-DOVE
  • PRINCIPAL DISPLAY PANEL

    Dove UGF Burst PDP
    Dove UGF Burst
  • INGREDIENTS AND APPEARANCE
    DOVE ULTIMATE GO FRESH BURST  ANTIPERSPIRANT AND DEODORANT
    aluminum zirconium tetrachlorohydrex gly stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1054
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Aluminum Zirconium Tetrachlorohydrex GLY (UNII: 8O386558JE) (Aluminum cation - UNII:3XHB1D032B) Aluminum Zirconium Tetrachlorohydrex GLY14.8 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    PPG-14 BUTYL ETHER (UNII: R199TJT95T)  
    HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)  
    STEARETH-100 (UNII: 4OH5W9UM87)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-1054-174 g in 1 CONTAINER
    2NDC:64942-1054-245 g in 1 CONTAINER
    3NDC:64942-1054-314 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)
    Establishment
    NameAddressID/FEIBusiness Operations
    Unilever Raeford HPCNA131411576manufacture
    Establishment
    NameAddressID/FEIBusiness Operations
    Unilever de Mexico S de RL de CV588151394manufacture
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!