Label: REFRESH ANTIBAC FOAM- benzalkonium chloride soap

  • NDC Code(s): 11084-010-01, 11084-010-05, 11084-010-12, 11084-010-20, view more
    11084-010-27, 11084-010-40, 11084-010-55, 11084-010-66, 11084-010-96
  • Packager: SC Johnson Professional USA, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 18, 2024

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  • Active ingredient

    BENZALKONIUM CHLORIDE, 0.13%

  • Purpose

    Antimicrobial

  • Uses

    for handwashing to reduce bacteria on the skin

  • Warnings

    For external use only

    When using this product

    avoid contact with eyes. In case of eye contact, flush with water.

    Stop use and ask a doctor if

    irritation and redness develop and persist for more than 3 days.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    apply foaming cleanser to dry hands
    rub hands together to spread lather
    wash for 15-20 seconds
    rinse & dry hands thoroughly

  • Inactive ingredients

    AQUA (WATER), GLYCERIN, LAURAMINE OXIDE, BUTYLENE GLYCOL, LACTIC ACID, SALICYLIC ACID, PARFUM (FRAGRANCE), GREEN 5 (CI 61570), YELLOW 5 (CI 19140).

  • PRINCIPAL DISPLAY PANEL - 1 L Bottle Label

    SCJ Professional
    A family company®

    NDC 11084-010-66

    Refresh™

    ANTIBAC FOAM

    Citrus Scent Antimicrobial Foam Handwash

    Manufactured for: SC Johnson Professional USA, Inc.
    Charlotte, NC 28217
    1-800-248-7190 www.scjp.com

    CITRUS FRAGRANCE

    deb
    SKIN CARE

    1 L
    (33.8 fl oz)

    Made in Canada
    L-1467 R0

    PRINCIPAL DISPLAY PANEL - 1 L Bottle Label
  • INGREDIENTS AND APPEARANCE
    REFRESH ANTIBAC FOAM 
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)  
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11084-010-400.4 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/12/201712/31/2024
    2NDC:11084-010-271 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/12/201712/31/2025
    3NDC:11084-010-121.2 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/12/2017
    4NDC:11084-010-202 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/12/2017
    5NDC:11084-010-053.78 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/12/2017
    6NDC:11084-010-010.047 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/27/201912/31/2024
    7NDC:11084-010-55208.2 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 0: Not a Combination Product02/27/201912/31/2024
    8NDC:11084-010-960.296 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/01/201912/31/2024
    9NDC:11084-010-661 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/31/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph drug505G(a)(3)06/12/2017
    Labeler - SC Johnson Professional USA, Inc. (607378015)
    Establishment
    NameAddressID/FEIBusiness Operations
    APEX International, Inc.015226132manufacture(11084-010)
    Establishment
    NameAddressID/FEIBusiness Operations
    SC Johnson Professional CA Inc.203765300MANUFACTURE(11084-010)
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