Label: MENS MITCHUM ADVANCED INVISIBLE ROLL-ON ANTIPERSPIRANT DEODORANT- aluminum zirconium tetrachlorohydrex gly liquid

  • 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 3, 2013

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

View All Sections
  • Drug Facts Active Ingredient

    Aluminum zirconium tetrachlorohydrex gly 20%

  • Purpose

    Antiperspirant

  • Use

    • Reduces underarm wetness
  • 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 irriation occurs

  • Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Apply to underarms only.

  • Inactive Ingredients

    aqua((water) eau), glyceryl stearate, laureth-23, magnesium aluminum silicate, polysorbate 20, tocopheryl acetate, aloe barbadensis leaf extract, hydrogen peroxide, silica dimethicone silylate, laureth-4, behentrimonium methosulfate, cetearyl alcohol, lauric acid, EDTA

  • Questions

    1-888-8-MITCHUM

  • Principal Display Panel - 1.7 fl oz bottle

    MM1

  • INGREDIENTS AND APPEARANCE
    MENS MITCHUM ADVANCED INVISIBLE  ROLL-ON ANTIPERSPIRANT DEODORANT
    aluminum zirconium tetrachlorohydrex gly liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10967-582
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE) (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY - UNII:8O386558JE) ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY0.20 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    LAURETH-23 (UNII: N72LMW566G)  
    MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    HYDROGEN PEROXIDE (UNII: BBX060AN9V)  
    SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)  
    LAURETH-4 (UNII: 6HQ855798J)  
    BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    LAURIC ACID (UNII: 1160N9NU9U)  
    EDETIC ACID (UNII: 9G34HU7RV0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10967-582-9750 mL in 1 BOTTLE, WITH APPLICATOR
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35012/15/2013
    Labeler - Revlon Consumer Products Corp (788820165)
    Establishment
    NameAddressID/FEIBusiness Operations
    Revlon South Africa (PTY) Ltd637155859manufacture(10967-582)
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!