Label: MITCHUM SMART SOLID- aluminum zirconium tetrachlorohydrex gly liquid liquid

  • NDC Code(s): 10967-613-25, 10967-614-25
  • Packager: Revlon Consumer Products Corp
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 12, 2024

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  • ACTIVE INGREDIENT

    Aluminum Zirconium Tetrachlorohydrex Gly 20%

  • Purpose

    Antiperspirant

  • 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 irriation occurs

  • KEEP OUT OF REACH OF CHILDREN

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

  • INACTIVE INGREDIENT

    Inactive Ingredients

    AQUA ((WATER) EAU), DIPROPYLENE GLYCOL, HYDROXYSTEARIC ACID, PEG-12 DIMETHICONE, GLYCERIN, CYCLOPENTASILOXANE, PARFUM (FRAGRANCE), ACETAMIDE MEA, AGAROSE, DIMETHICONE CROSSPOLYMER, LINALOOL, HEXYL CINNAMAL, ALPHA-ISOMETHYL IONONE, XYLITOL, CITRONELLOL, LIMONENE, CINNAMYL ALCOHOL, BENZYL CINNAMATE

  • INDICATIONS & USAGE

    Reduces underarm wetness

  • DOSAGE & ADMINISTRATION

  • PRINCIPAL DISPLAY PANEL

    Mitchum Smart Solid

    Clinical Performance

    Net wt. 2.5oz/ 70g

    1103-15

  • PRINCIPAL DISPLAY PANEL

    Mitchum Smart Solid
    Clinical Performance
    Net wt. 2.5oz/ 70g

    1103-018

  • INGREDIENTS AND APPEARANCE
    MITCHUM SMART SOLID 
    aluminum zirconium tetrachlorohydrex gly liquid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10967-613
    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 GLY0.2 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
    GERANIOL (UNII: L837108USY)  
    LIMONENE, (+/-)- (UNII: 9MC3I34447)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    WATER (UNII: 059QF0KO0R)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    12-HYDROXYSTEARIC ACID (UNII: 933ANU3H2S)  
    PEG-12 DIMETHICONE (UNII: ZEL54N6W95)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CYCLOHEXYL CINNAMATE (UNII: 2955WP594O)  
    ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)  
    XYLITOL (UNII: VCQ006KQ1E)  
    CINNAMYL ALCOHOL (UNII: SS8YOP444F)  
    BENZYL CINNAMATE (UNII: V67O3RO97U)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    ACETIC MONOETHANOLAMIDE (UNII: A9O0818TWD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10967-613-2573 mL in 1 CONTAINER; Type 0: Not a Combination Product12/01/2009
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01912/01/2009
    MITCHUM SMART SOLID 
    aluminum zirconium tetrachlorohydrex gly liquid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10967-614
    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 GLY0.2 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    12-HYDROXYSTEARIC ACID (UNII: 933ANU3H2S)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CYCLOHEXYL CINNAMATE (UNII: 2955WP594O)  
    ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)  
    XYLITOL (UNII: VCQ006KQ1E)  
    CINNAMYL ALCOHOL (UNII: SS8YOP444F)  
    BENZYL CINNAMATE (UNII: V67O3RO97U)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    ACETIC MONOETHANOLAMIDE (UNII: A9O0818TWD)  
    .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
    GERANIOL (UNII: L837108USY)  
    LIMONENE, (+/-)- (UNII: 9MC3I34447)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    PEG-12 DIMETHICONE (UNII: ZEL54N6W95)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10967-614-2573 mL in 1 CONTAINER; Type 0: Not a Combination Product12/01/2009
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01912/01/2009
    Labeler - Revlon Consumer Products Corp (788820165)
    Establishment
    NameAddressID/FEIBusiness Operations
    REVLON, INC.809725570manufacture(10967-613, 10967-614)
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