Label: HAND ANTIPERSPIRANT DAILY USE- aluminum zirconium octachlorohydrex gly cream

  • 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 June 1, 2020

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  • ACTIVE INGREDIENT

    Active Ingredient Purpose

    Aluminum Zirconium Tetrachlorohydrex Gly (20%) Antiperspirant

  • PURPOSE

    Use

    reduces perspiration

  • KEEP OUT OF REACH OF CHILDREN

    Keep out reach of children. If swallowed get medical help or contact a Poison Control Center right away

  • INDICATIONS & USAGE

    Stop use if rash or irritation occurs

  • WARNINGS

    Warnings

    For external use only.

    Do not use on broken or irritated skin

    Ask a doctor before use if you have kidney disease.

  • DOSAGE & ADMINISTRATION

    Directions

    • wash and dry hands thoroughly before application
    • Apply a single pump of product to palms each morning
    • Rub Balms together vigorously for 30 seconds
  • INACTIVE INGREDIENT

    Inactive Ingredients Aluminum Starch Octenylsuccinate, Aqua (water), Cetyl Hydroxyethylcellulose, Coco-Caprylate/Caprate.Coconut Alkanes, Disodium EDTA, Ethylhexylglycerin, Glycerin, Helianthus Annuus (Suflower) Extract, Hydroxypropyl Starch Phosphate, Octenidine HCL, Oryza SAtiva (Rice) Bran Extract, Phenoxyethanol, Polymethylsilsesquioxane, Propanediol, Propylene Glycol, Rosmarinus Officinalis (Rosemary) Leaf Extract, SD Alcohol 40-B, SIlica, Sodium Hydroxide, Tocopherol, Xanthan Gum

  • PRINCIPAL DISPLAY PANEL

    Carpe

    Clinical Grade HAND

    Antiperspirant

    Daily Use

    20% Aluminum Zirconium Octachlorohydrex GLY

    Daily Use Carpe

  • INGREDIENTS AND APPEARANCE
    HAND ANTIPERSPIRANT DAILY USE 
    aluminum zirconium octachlorohydrex gly cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74307-007
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY (UNII: P9D3YP29MY) (ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY - UNII:P9D3YP29MY) ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY20 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
    CETYL HYDROXYETHYLCELLULOSE (350000 MW) (UNII: T7SWE4S2TT)  
    COCONUT ALKANES (UNII: 1E5KJY107T)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    OCTENIDINE HYDROCHLORIDE (UNII: U84956NU4B)  
    RICE BRAN (UNII: R60QEP13IC)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    ROSEMARY (UNII: IJ67X351P9)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)  
    COCOYL CAPRYLOCAPRATE (UNII: 8D9H4QU99H)  
    WATER (UNII: 059QF0KO0R)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74307-007-0130 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35006/01/2020
    Labeler - Clutch Inc (080214892)
    Establishment
    NameAddressID/FEIBusiness Operations
    Wasatch Product Development, LLC.962452533manufacture(74307-007)
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