Label: DEB INSTANTFOAM COMPLETE- alcohol liquid

  • NDC Code(s): 11084-170-01, 11084-170-12, 11084-170-27, 11084-170-40
  • 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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  • Active ingredient

    ETHYL ALCOHOL, 80% w/w

  • Purpose

    Antibacterial

  • Uses

    for hand sanitizing to reduce bacteria on the skin

  • 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.

  • Directions

    apply foaming sanitizer to cover hands

    rub into skin

    no rinsing required

  • Inactive ingredients

    AQUA (WATER), BIS-PEG-12 DIMETHICONE, CITRIC ACID, COCO-GLUCOSIDE, DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE, GLYCERYL OLEATE, PANTHENOL, PEG-200 HYDROGENATED GLYCERYL PALMITATE, PEG-7 GLYCERYL COCOATE

  • PRINCIPAL DISPLAY PANEL

    deb stoko

    NDC 11084-170-27

    Deb InstantFOAM Complete

    EN Broad Spectrum Alcohol-Based Instant Hand Sanitizer Foam with Moisturizer and Skin Conditioner

    Perfume-free   Dye-free   No water required  Kills 99.999% of many types of common germs

    ES Amplio espectro antiseptico con alcohol para manos en espuma y con acondicionador

    Sin perfume   Sin colorante   No se requiere agua   Elimina el 99.999% de los muchos tipos de germenes mas comunes

    SANITIZE

    deb

    Stock #:

    IFC1L

    Made in / Hecho en Canada

    US Patents 5,445,288 & 6,082,586

    Worldwide Patent Pending.

    Made by Deb for:

    Deb USA, Inc.

    Charlotte, NC 28217

    1-800-248-7190

    www.debgroup.com

    DCN9207/0715

    1 L

    (33.8 fl oz)

    Meets food code hand sanitizer criteria (Section 2-301.16) published by the FDA

    IFC1L-DCN9207/0715

    IFC1L-DCN9207/0715

  • INGREDIENTS AND APPEARANCE
    DEB INSTANTFOAM COMPLETE 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-170
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.80 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    BIS-PEG-12 DIMETHICONE (500 MPA.S) (UNII: 2CNS542YRT)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    COCO-GLUCOSIDE (UNII: ICS790225B)  
    DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)  
    GLYCERYL OLEATE (UNII: 4PC054V79P)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    PEG-200 HYDROGENATED GLYCERYL PALMATE (UNII: W161T051Y1)  
    PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11084-170-0147 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/18/201512/31/2024
    2NDC:11084-170-40400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/18/201512/31/2024
    3NDC:11084-170-271000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/18/201512/31/2024
    4NDC:11084-170-121000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/18/201512/31/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph drug505G(a)(3)08/18/201512/31/2024
    Labeler - SC Johnson Professional USA, Inc. (607378015)
    Registrant - SC Johnson Professional USA, Inc. (078805627)
    Establishment
    NameAddressID/FEIBusiness Operations
    SC Johnson Professional CA Inc.203765300manufacture(11084-170)
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