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

  • NDC Code(s): 11084-300-01, 11084-300-12, 11084-300-27, 11084-300-40, view more
    11084-300-66, 11084-300-97
  • Packager: SC Johnson Professional USA, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 18, 2024

If you are a consumer or patient please visit this version.

View All Sections
  • 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, Cocamidopropyl Betaine, Lauramine Oxide, Phenoxyethanol, Propylene Glycol, Tetrasodium EDTA

  • PRINCIPAL DISPLAY PANEL - 1 L Bottle Label

    SCJ PROFESSIONAL
    A Family Company™

    NDC 11084-300-27

    InstantFOAM™ Non-Alcohol PURE

    HAND SANITIZER
    Alcohol-Free FOAM Hand sanitizer - Dye & Perfume-Free

    Stock #: 55857/4000007087

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

    1 L (33.8 fl oz)

    deb
    SKIN CARE

    1000003036/0220

    PRINCIPAL DISPLAY PANEL - 1 L Bottle Label
  • INGREDIENTS AND APPEARANCE
    INSTANT FOAM NON-ALCOHOL PURE HAND SANITIZER 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-300
    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)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11084-300-271000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/15/202012/31/2024
    2NDC:11084-300-121200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/15/2020
    3NDC:11084-300-97296 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/15/202012/31/2024
    4NDC:11084-300-0147 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/15/202012/31/2024
    5NDC:11084-300-40400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/01/202012/31/2024
    6NDC:11084-300-661000 mL in 1 BOTTLE; Type 0: Not a Combination Product02/17/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph drug505G(a)(3)04/15/2015
    Labeler - SC Johnson Professional USA, Inc. (607378015)
    Establishment
    NameAddressID/FEIBusiness Operations
    APEX International, Inc.015226132MANUFACTURE(11084-300)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!