Label: APPEAL ALCOHOL FOAMING HAND SANITIZER- ethyl alcohol liquid

  • NDC Code(s): 11084-702-27
  • 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 December 11, 2020

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

View All Sections
  • 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 one shot of foaming sanitizer to dry hands

    Rub into skin

    No rinsing required

  • INACTIVE INGREDIENT

    Inactive ingredients

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

  • PRINCIPAL DISPLAY PANEL

    container label

    APP17102

    102668

    appeal Alcohol Foaming Hand Sanitizer

    Certified EcoLogo

    Certified Instant Hand Antiseptic CCD-170

    1 Liter

    33.8 Fluid Ounces

    Made in Canada by Deb

    deb foam technolody

    Distributed exclusively by:

    Interline Brands

    Jacksonville, FL  32207

    www.AppealProducts.com

    Rev. 05-12

    01830

    container label

    container label

  • INGREDIENTS AND APPEARANCE
    APPEAL ALCOHOL FOAMING HAND SANITIZER 
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-702
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol70 mL  in 100 mL
    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:11084-702-271000 mL 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(11084-702)
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!