Label: ADVANCED ANTIBACTERIAL FOAMING HAND SOAP- benzalkonium chloride solution

  • NDC Code(s): 47593-543-41, 47593-543-44, 47593-543-59, 47593-543-60, view more
    47593-543-63
  • Packager: Ecolab Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 30, 2023

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  • Active Ingredient

    Benzalkonium chloride 0.5%

  • Purpose

    Antiseptic handwash

  • Uses

    • for handwashing to decrease bacteria on the skin
  • Warning

    • For external use only

    Do not use

    • in eyes

    When using the 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 hands and apply foam
    • scrub hands and forearms
    • rinse thoroughly and dry
  • Other information

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

    Inactive ingredients water (aqua), cocamine oxide, hexylene glycol, PEG-180, glycerin, cocamidopropyl PG-dimonium chloride phosphate, myristamine oxide, phenoxyethanol, polyquaternium 7, citric acid, myristamide DIPA, methyl gluceth-20, caprylic/capric glycerides, PEG-12 dimethicone, potassium hydroxide, fragrance, FD&C blue 1

  • QUESTIONS

    Questions? call 1-866-781-8787

  • Representative Label and Principal Display Panel

    Ecolab®

    6101088

    Advanced Antibacterial Foaming

    Hand Soap

    1250 mL (42.3 US FL OZ)

    Active ingredient

    Benzalkonium chloride 0.5%

    Ecolab · 1 Ecolab Place · St. Paul MN 55102 USA ·

    tel: 1 800 35 CLEAN (352 5326)

    © 2020 Ecolab USA Inc. · All rights reserved

    Made in U.S.A.

    www.ecolab.com

    Representative label

  • INGREDIENTS AND APPEARANCE
    ADVANCED ANTIBACTERIAL FOAMING HAND SOAP 
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47593-543
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
    PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    METHYL GLUCETH-20 (UNII: J3QD0LD11P)  
    MYRISTIC DIISOPROPANOLAMIDE (UNII: 17DN142CTK)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 900000 MW) (UNII: B70CUU14M9)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    MYRISTAMINE OXIDE (UNII: J086PM3RRT)  
    COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    WATER (UNII: 059QF0KO0R)  
    COCAMINE OXIDE (UNII: QWA2IZI6FI)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47593-543-601600 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/12/2015
    2NDC:47593-543-631250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/12/2015
    3NDC:47593-543-591250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/12/2015
    4NDC:47593-543-41750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/12/2015
    5NDC:47593-543-441134000 mL in 1 CONTAINER; Type 0: Not a Combination Product08/12/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)08/12/2015
    Labeler - Ecolab Inc. (006154611)
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