Label: ECOLAB- benzalkonium chloride solution

  • NDC Code(s): 47593-532-41, 47593-532-59
  • Packager: Ecolab Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated July 30, 2024

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  • Active ingredient

    Benzalkonium Chloride 0.55%

  • Purpose

    Antiseptic handwash

  • Uses

    • for handwashing to decrease bacteria on the skin
  • Warnings

    For external use only

    Do not use

    • In eyes

    When using this product 

    • if in eyes, rinse promptly and thoroughly with water.
    • discontinue use if irritation and redness develop.

    Stop use and ask a doctor if skin irritation or redness occurs 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 spread a small amount on hands and forearms
    • scrub well, rinse thoroughly and dry
  • Other information

    • for additional information, see Safety Data Sheet (SDS)
    • EMERGENCY HEALTH INFORMATION: 1 800 328 0026. If located outside the United States and Canada, call collect 1 651 222 5352 (number is in the US).
  • INACTIVE INGREDIENT

    Inactive ingredients: water (aqua), hexylene glycol, cocamine oxide, PEG-180, glycerin, cocamidopropyl PG-dimonium chloride phosphate, methyl gluceth-20, phenoxyethanol, myristamide DIPA, caprylic/capric glycerides, citric acid, hydroxypropyl guar hydroxypypropyltrimonium chloride, PEG-12 dimethicone, ethanol, tocopheryl acetate, fragrance, potassium hydroxide

  • QUESTIONS

    Questions? call 1-800-35-CLEAN (352-5326)

  • Principal display panel and representative label

    6100958

    Premium Antibacterial Foam Hand Soap

    Active ingredient: Benzalkonium Chloride, 0.55%

    761095/5401/0321

    1250 mL (42 US FL OZ)

    Ecolab · 1 Ecolab Place · St. Paul MN 55102

    USA ·tel: 1 800 35 CLEAN (352 5326)

    © 2021 Ecolab USA Inc. · All rights reserved

    Made in U.S.A.

    www.ecolab.com

    representative label

  • INGREDIENTS AND APPEARANCE
    ECOLAB 
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47593-532
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE5.5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    COCAMINE OXIDE (UNII: QWA2IZI6FI)  
    POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
    METHYL GLUCETH-20 (UNII: J3QD0LD11P)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    MYRISTIC DIISOPROPANOLAMIDE (UNII: 17DN142CTK)  
    GLYCERYL MONO- AND DICAPRYLOCAPRATE (UNII: U72Q2I8C85)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    GUAR GUM (UNII: E89I1637KE)  
    PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)  
    ALCOHOL (UNII: 3K9958V90M)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47593-532-591250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/28/2016
    2NDC:47593-532-41750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/28/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)04/28/2016
    Labeler - Ecolab Inc. (006154611)
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