Label: DEB INSTANTFOAM ALCOHOL SANITIZER- ethyl alcohol liquid

  • NDC Code(s): 11084-703-02, 11084-703-12, 11084-703-27, 11084-703-40
  • Packager: SC Johnson Professional USA, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated April 26, 2019

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  • ACTIVE INGREDIENT

    Active ingredient

    Ethyl Alcohol 70% ww

  • PURPOSE

    Purpose

    Antibacterial

  • INDICATIONS & USAGE

    Uses

    For hand sanitizing to reduce bacteria on the skin

  • WARNINGS

    Warnings

    For external use only

    Flammable: Keep away from fire or flame.

    When using this product avoid contact with eyes.  In case of eye contact, flush with water.

    Keep out of reach of children.

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

  • DOSAGE & ADMINISTRATION

    Directions

    Apply foaming sanitizer to cover hands

    Rub into skin

    No need to rinse

  • INACTIVE INGREDIENT

    Inactive ingredients

    AQUA (Water), Bis-PEG-12 Dimethicone, Behentrimonium Chloride, PEG-200 Hydrogenated Glyceryl Palmate, PEG-7 Glyceryl Cocoate, Coco-Glucoside, Glyceryl Oleate, Dihydroxypropyl PEG-5 Linoleammonium Chloride.

  • PRINCIPAL DISPLAY PANEL

    NDC 11084-703-27

    deb stoko

    Deb InstantFOAM

    Alcohol Hand Sanitizer
    No Water Required | Kills 99.999% of Common Germs

    Antiséptico para manos en espuma - con alcohol
    No se requiere agua | Elimina el 99.999% de los gérmenes más
    comunes

    SANITIZE

    1 L (33.8 FL OZ)

    Stock #IFS1L

    Deb USA, Inc., 1-800-248-7190, www.debgroup.com

    Made in Canada, DCN9313 L-1251 R6

    OPEN FOR DRUG FACTS

    IFS1L-DCN9313 InstantFOAM Sanitizer-L1251R6-V8

  • INGREDIENTS AND APPEARANCE
    DEB INSTANTFOAM ALCOHOL SANITIZER 
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-703
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol70 L  in 100 L
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)  
    BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    COCO GLUCOSIDE (UNII: ICS790225B)  
    PEG-200 DILAURATE (UNII: TWV5J70L88)  
    GLYCERYL COCOATE (UNII: WVK1CT5994)  
    GLYCERYL MONOOLEATE (UNII: C4YAD5F5G6)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11084-703-271 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/15/2012
    2NDC:11084-703-121 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/15/2012
    3NDC:11084-703-40.4 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/15/2012
    4NDC:11084-703-02.047 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/15/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E05/15/2012
    Labeler - SC Johnson Professional USA, Inc. (607378015)
    Establishment
    NameAddressID/FEIBusiness Operations
    SC Johnson Professional CA Inc.203765300manufacture(11084-703)
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