Label: ECOLAB- benzalkonium chloride solution

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated August 5, 2024

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  • Active ingredient

    Benzalkonium Chloride, 0.55%

  • Purpose

    Antiseptic handwash

  • Uses

    • For handwashing to decrease bacteria on the skin
    • Recommended for repeated use.

  • 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 around on hands and forearms
    • scrub well, rinse thoroughly and dry
  • Other information

    • for additional information, see Safety Data Sheet (SDS)
    • for emergency medical information in USA, call 1 800 328 0026
  • INACTIVE INGREDIENT

    Inactive ingredients water (aqua), laurtrimonium chloride, capryloyl/caproyl methyl glucamide, phenoxyethanol, propylene glycol, cocamidopropyl PG-dimonium chloride phosphate, glycerin, palmitamidopropyltrimonium chloride, methyl gluceth-20, trisodium dicarboxymethyl alaninate, alcohol, hydroxyethylcellulose

  • QUESTIONS

    Questions? call 1 866 781 8787

  • Prinicpal Display Panel / Representative Label

    ECOLAB®

    Antimicrobial Foaming Hand Soap
    Active Ingredient: 0.55% Benzalkonium Chloride
    Net Contents: 750 mL (25 fl oz)

    This product may be patented:
    www.ecolab.com/patents

    Ecolab · 1 Ecolab Place · St. Paul MN 55102 USA
    © 2017 Ecolab USA Inc. · All rights reserved
    Made in United States
    www.ecolab.com

    representative label

  • INGREDIENTS AND APPEARANCE
    ECOLAB 
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47593-593
    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)  
    LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    DECANOYL N-METHYLGLUCAMIDE (UNII: 9Q27ZA5M8G)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PALMITAMIDOPROPYLTRIMONIUM CHLORIDE (UNII: N2U96D202F)  
    METHYL GLUCETH-20 (UNII: J3QD0LD11P)  
    TRISODIUM DICARBOXYMETHYL ALANINATE (UNII: 784K2O81WY)  
    ALCOHOL (UNII: 3K9958V90M)  
    HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (UNII: S38J6RZN16)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47593-593-41750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/16/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)05/16/2018
    Labeler - Ecolab Inc. (006154611)
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