Label: KLAR AND DANVER ANTIBACTERIAL HAND  - benzalkonium chloride soap 

  • Label RSS
  • NDC Code(s): 33992-8000-0, 33992-8000-1
  • Packager: Greenbrier International, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 12/13

If you are a consumer or patient please visit this version.

  • KLAR & DANVER ANTIBACTERIAL LIQUID HAND SOAP
  • Active Ingredient

    Benzalkonium Chloride 0.10%

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  • Purpose

    Antibacterial

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  • Use:

    Handwashing to decrease bacteria on skin.

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  • Warnings:

    For external use only.

    When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.

    Stop use and ask a doctor if irritation or redness develop or increase.

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

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  • Directions:

    • Wet hands, work into a rich lather
    • Rinse well.
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  • Inactive Ingredients:

    WATER, SODIUM LAURYL ETHER SULFATE, COCAMIDOPROPYL BETAINE, SODIUM CHLORIDE, POLYQUATERNIUM-7, FRAGRANCE, METHYLISOTHIAZOLINONE, METHYLCHLOROISOTHIASOLINONE, CITRIC ACID, GLUTARIC DIALDEHYDE, TETRASODIUM EDTA, TOCOPHERYL ACETATE (VITAMIN E), ALOE BARBADENSIS LEAF EXTRACT, FD C ORANGE 7 (CI 15510).

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  • DISTRIBUTED BY

    GREENBRIER INTERNATIONAL, INC.

    500 VOLVO PARKWAY, CHESAPEAKE, VA 23320

    MADE IN  MEXICO

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  • PRINCIPAL DISPLAY PANEL

    KLAR and DANVER ANTIBACTERIAL LIQUID HAND SOAP 1,584 Bottles (443ml each) (33992-8000-0)

    Label


    KLAR and DANVER ANTIBACTERIAL LIQUID HAND SOAP 1,210 Bottles (591ml each) (33992-8000-1)

    Label20oz







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  • INGREDIENTS AND APPEARANCE
    KLAR AND DANVER ANTIBACTERIAL HAND  
    benzalkonium chloride soap
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:33992-8000
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 1 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    SODIUM LAURYL SULFATE  
    COCAMIDOPROPYL BETAINE  
    SODIUM CHLORIDE  
    METHYLISOTHIAZOLINONE  
    METHYLCHLOROISOTHIAZOLINONE  
    CITRIC ACID MONOHYDRATE  
    EDETATE SODIUM  
    .ALPHA.-TOCOPHEROL ACETATE  
    ALOE VERA LEAF  
    D&C ORANGE NO. 4  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:33992-8000-0 1584 in 1 CONTAINER
    1 443 mL in 1 BOTTLE
    2 NDC:33992-8000-1 1210 in 1 CONTAINER
    2 591 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333E 08/28/2013
    Labeler - Greenbrier International, Inc. (610322518)
    Establishment
    Name Address ID/FEI Business Operations
    4e De Mexico SA de CV 813022811 manufacture(33992-8000)
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