Label: EOUX DEODORANT- aluminum chlorohydrate emulsion

  • 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 May 23, 2012

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  • ACTIVE INGREDIENT

    This product is owned as a deodorant active ingredients triclosan and aluminum chlorhydroxide. Mixed effect that produced is deodorant and antiperspirant.
  • PURPOSE

    Eoux is an anti-bacterial and antiperspirant high protection modern biotechnical design deodorant.

  • KEEP OUT OF REACH OF CHILDREN

    This product must be keep out reach of the children.

  • INDICATIONS & USAGE

    This product is designed for use in armpit areas as may cause irritation in the area of application by the sensitivity of the user.

  • WARNINGS

    Hypersensivity may result in the area of application, not consume this product, if swallowed consult your doctor.

  • DOSAGE & ADMINISTRATION

    This product is topical application apply the amount necessary in desirable area and rub gently.

  • INACTIVE INGREDIENT

    The design of this product does humectant agents to give best feeling in the skin effect in addition to produce antiperspirant and deodorant.

  • PRINCIPAL DISPLAY PANEL

    IMAGE OF THE LABEL
    IMAGE OF THE LABEL
  • INGREDIENTS AND APPEARANCE
    EOUX  DEODORANT
    aluminum chlorohydrate emulsion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66854-009
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE280 mL  in 1000 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    STEARETH-2 (UNII: V56DFE46J5)  
    CETEARETH-12 (UNII: 7V4MR24V5P)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
    DISTEARYL ETHER (UNII: SC6T3MJF8Y)  
    PPG-3 MYRISTYL ETHER (UNII: 7913J43WZ5)  
    CYCLOMETHICONE (UNII: NMQ347994Z)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)  
    DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    DIPYRITHIONE (UNII: 9L87N86R9A)  
    ALLANTOIN (UNII: 344S277G0Z)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    TRICLOSAN (UNII: 4NM5039Y5X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66854-009-0190 mL in 1 JAR
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35005/31/2012
    Labeler - SPAI SONS PHARMACEUTICAL INTERNATIONAL COSMETICS (880172184)
    Registrant - SPAI SONS PHARMACEUTICAL INTERNATIONAL COSMETICS (880172184)
    Establishment
    NameAddressID/FEIBusiness Operations
    SPAI SONS PHARMACEUTICAL INTERNATIONAL COSMETICS880172184analysis, label, manufacture, pack
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