Label: BACTI-FOAM- triclosan solution 

  • Label RSS
  • NDC Code(s): 47593-169-38, 47593-169-41, 47593-169-56
  • Packager: Ecolab 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 05/13

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

  • Active Ingredient

    Triclosan, 0.3%

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  • Purpose

    Healthcare personnel handwash

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  • Uses

    • healthcare personnel handwash
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  • Warnings

    For external use only

    When using this product

    • discontinue use if irritation and redness develop

    Stop use and ask Doctor if

    • irritation and redness persist for more than 72 hours

    ​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 skin and apply a small amount on hands and forearms
    • scrub well, rinse thoroughly and dry
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  • Other information

    • for emergency medical information in USA and Canada, call 1.800.328.0026
    • for emergency medical information worldwide, cal 1.651.222.5352 (in the USA)
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  • INACTIVE INGREDIENT

    ​Inactive ingredients water, potassium cocoate, SD alcohol 40-B, glycerin, potassium stearate, tetrasodium EDTA, cocamidopropyl PG-dimonium chloride phosphate, cocamine oxide, fragrance, methylparaben, tocopheryl acetate, citric acid, potassium hydroxide, isopropyl alcohol, propylparaben, aloe barbadensis leaf juice, FDC blue 1, FDC yellow 5

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  • QUESTIONS

    Questions? call​ 1.866.781.8787

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  • Principal Display Panel and Representative Label

    ECOLAB

    BACTI-FOAM®

    NDC 47593-169-56

    DIN 02237409

    Antimicrobial Foam Hand Soap

    Healthcare Peronnel Handwash

    Active Ingredient:  0.3% Triclosan

    Nets Contents:

    1200 mL (40.6 fl oz)

    6082565

    747795/8502/1012

    representative labelrepresentative label

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  • INGREDIENTS AND APPEARANCE
    BACTI-FOAM 
    triclosan solution
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:47593-169
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Triclosan (Triclosan) Triclosan 3 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    POTASSIUM COCOATE  
    ALCOHOL  
    GLYCERIN  
    POTASSIUM STEARATE  
    EDETATE SODIUM  
    COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE  
    COCAMINE OXIDE  
    METHYLPARABEN  
    .ALPHA.-TOCOPHEROL ACETATE  
    CITRIC ACID MONOHYDRATE  
    POTASSIUM HYDROXIDE  
    ISOPROPYL ALCOHOL  
    PROPYLPARABEN  
    ALOE VERA LEAF  
    FD&C BLUE NO. 1  
    FD&C YELLOW NO. 5  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:47593-169-38 500 mL in 1 BOTTLE, PLASTIC
    2 NDC:47593-169-41 750 mL in 1 BOTTLE, PLASTIC
    3 NDC:47593-169-56 1200 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333E 07/11/1997
    Labeler - Ecolab Inc. (006154611)
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