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Bacti-Foam (Ecolab Inc.)

Available Formats

Dosage Form Package Information Links
SOLUTION 1200 mL in 1 BOTTLE, PLASTIC (47593-169-56) Label Information
SOLUTION 750 mL in 1 BOTTLE, PLASTIC (47593-169-41) Label Information
SOLUTION 500 mL in 1 BOTTLE, PLASTIC (47593-169-38) Label Information

Complete Bacti-Foam Information

  • Active Ingredient

    Triclosan, 0.3%


  • Purpose

    Healthcare personnel handwash


  • Uses

    • healthcare personnel handwash

  • Warnings

    • For external use only

    When using this product
    • discontinue use if irritation and redness develop

    Stop use and ask Doctor if
    • skin 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.


  • Directions

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

  • 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)

  • 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


  • QUESTIONS

    Questions? call​ 1.866.781.8787


  • Principal Display Panel and Representative Label

    ECOLAB®

    NDC 47593-169-56
    DIN 02237409

    BACTI-FOAM®

    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 label


  • INGREDIENTS AND APPEARANCE
    BACTI-FOAM 
    triclosan solution
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:47593-169
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X) Triclosan 3 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    POTASSIUM COCOATE (UNII: F8U72V8ZXP)  
    ALCOHOL (UNII: 3K9958V90M)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POTASSIUM STEARATE (UNII: 17V812XK50)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
    COCAMINE OXIDE (UNII: QWA2IZI6FI)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:47593-169-38 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/08/2012
    2 NDC:47593-169-41 750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/13/2013
    3 NDC:47593-169-56 1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/30/2009
    4 NDC:47593-169-59 1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/30/2009
    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)