Label: INSTANT FOAM NON-ALCOHOL HAND SANITIZER- benzalkonium chloride liquid

  • NDC Code(s): 11084-301-27, 11084-301-40, 11084-301-66, 11084-301-97
  • Packager: SC Johnson Professional USA, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 17, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Benzalkonium Chloride, 0.13%

  • Purpose

    Antiseptic

  • Uses

    • to decrease bacteria on the skin that could cause disease
  • Warnings

    For external use only

    When using this product

    • Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
    • Avoid contact with broken skin.
    • Do not inhale or ingest.

    Stop use and ask a doctor if

    • irritation and redness develop
    • condition persists 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 thouroughly with product and allow to dry without wiping.
    • For children under 6, use only under adult supervision.
  • Inactive ingredients

    Aqua (Water), Aloe Barbadensis Leaf Juice, Caprylyl Glycol, Citric Acid, Cocamidopropyl Betaine, Lauramine Oxide, Parfum (Fragrance), Phenoxyethanol, Propylene Glycol, Tetrasodium EDTA, Blue 1 (CI 42090), Red 33 (CI 17200)

  • PRINCIPAL DISPLAY PANEL - 1000 mL Bottle Label

    SCJ PROFESSIONAL
    A Family Company™

    NDC 11084-301-27

    InstantFOAM™ Non-Alcohol

    HAND SANITIZER
    Alcohol-Free FOAM Hand Sanitizer - Fragranced

    PRINCIPAL DISPLAY PANEL - 1000 mL Bottle Label
  • INGREDIENTS AND APPEARANCE
    INSTANT FOAM NON-ALCOHOL HAND SANITIZER 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-301
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11084-301-271000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/15/202012/31/2024
    2NDC:11084-301-97296 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/15/202012/31/2024
    3NDC:11084-301-40400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/01/202012/31/2024
    4NDC:11084-301-661000 mL in 1 BOTTLE; Type 0: Not a Combination Product02/17/202312/31/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph drug505G(a)(3)04/15/201512/31/2024
    Labeler - SC Johnson Professional USA, Inc. (607378015)
    Establishment
    NameAddressID/FEIBusiness Operations
    APEX International, Inc.015226132MANUFACTURE(11084-301)
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