Label: HAND ANTIPERSPIRANT NIGHTLY USE- aluminum chloride hexahydrate cream

  • Category: HUMAN OTC DRUG LABEL

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 Chloride Hexahydrate (15%) Anti-perspirant

  • 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 and ask a doctor 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 palms 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

    Nightly Use

    15% Aluminum Chloride

    Nightly Use Carpe

  • INGREDIENTS AND APPEARANCE
    HAND ANTIPERSPIRANT NIGHTLY USE 
    aluminum chloride hexahydrate cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74307-008
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM CHLORIDE15 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)  
    OCTENIDINE HYDROCHLORIDE (UNII: U84956NU4B)  
    ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
    COCONUT ALKANES (UNII: 1E5KJY107T)  
    COCOYL CAPRYLOCAPRATE (UNII: 8D9H4QU99H)  
    WATER (UNII: 059QF0KO0R)  
    CETYL HYDROXYETHYLCELLULOSE (350000 MW) (UNII: T7SWE4S2TT)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    ROSEMARY (UNII: IJ67X351P9)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    RICE BRAN (UNII: R60QEP13IC)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74307-008-0130 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(74307-008)
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