Label: ANTIPERSPIRANT MAXIMUM SECURITY- aluminum zirconium tetrachlorohydrex stick

  • 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 December 20, 2018

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  • ACTIVE INGREDIENT

    Active ingredient Purpose

    Aluminum Zirconium tetrachlorohydrex Gly 8.6% W/W Antiperspirant

  • PURPOSE

    Use reduces underarm perspiration

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of 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 skin

  • DOSAGE & ADMINISTRATION

    Directions apply to underarms only

  • INACTIVE INGREDIENT

    Inactive ingredients

    Propylene glycol, fragrance, dibenzylidene sorbitol, diisopropyl sebacate, hydroxypropyl cellulose, PEG/PPG-14/4 dimethicone, tetrasodium EDTA.

  • PRINCIPAL DISPLAY PANEL

    Maximum Security

    Antiperspirant

    Regular

    Net WT. 2.5 oz (70g)

    image description

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  • INGREDIENTS AND APPEARANCE
    ANTIPERSPIRANT  MAXIMUM SECURITY
    aluminum zirconium tetrachlorohydrex stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:22431-641
    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 GLY6.02 g  in 70 g
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    DIISOPROPYL SEBACATE (UNII: J8T3X564IH)  
    HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:22431-641-0170 g in 1 TUBE; Type 0: Not a Combination Product06/07/2011
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35006/07/2011
    Labeler - Blue Cross Labs (008298879)
    Registrant - Blue Cross Labs (008298879)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhejiang Greenface Housewares Co.,Ltd527999264manufacture(22431-641)