Label: VETI-FOAM- benzethonium chloride liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not 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 December 28, 2011

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  • Active ingredient(s)

     Benzethonium Chloride 0.20%

  • Purpose

  • Use(s)

     for hand washing to decrease bacteria on skin

  • Warnings

    For external use only

    Do not use

    Ask a doctor before use if

    Ask a doctor or pharmacist before use if

    When using this product

    •  Avoid contact with eyes; in case of contact, thoroughly rinse eyes with water.  Seek medical attention if irritation persists.

    Stop use and ask a doctor if

    • skin rash or redness develops when using this product 

    Pregnancy/Breastfeeding

    Keep out of reach of children

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

  • Directions

     Use 1-2 pumps of product on plam.  Rub lather completely around hands and between fingers.  Scrub thoroughly and rinse with water.

  • Other information

  • Storage

  • Inactive ingredients

     Aloe barbadensis (Aloe Vera) Leaf Juice, Ammonium lauryl Sulfate, Cocamidoprpyl Betaine, DMDM Hydantoin, FD&C Blue #1, Fragrance, Glycerin, Purified Water, EDTA

  • Questions

  • Principal Display Panel

    16oz label

    16oz label

  • INGREDIENTS AND APPEARANCE
    VETI-FOAM 
    benzethonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:13985-529
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE2.0 g  in 1.0 L
    Inactive Ingredients
    Ingredient NameStrength
    EDETATE SODIUM (UNII: MP1J8420LU)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Product Characteristics
    ColorBLUEScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:13985-529-160.473 L in 1 BOTTLE, PUMP
    2NDC:13985-529-013.785 L in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart333A07/26/2010
    Labeler - MWI/Vet One (019926120)
    Registrant - Continental Manufacturing Chemist, Inc. (005278007)
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