Label: APPEAL ANTIBACTERIAL HAND WASH- benzalkonium chloride solution

  • NDC Code(s): 11084-015-27, 11084-015-66
  • Packager: SC Johnson Professional USA, Inc.
  • Category: HUMAN OTC DRUG LABEL

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 February 27, 2023

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • Active ingredient

    BENZALKONIUM CHLORIDE, 0.13%

  • Purpose

    Antibacterial

  • Uses

    for handwashing to reduce bacteria on the skin

  • Warnings

    For external use only

    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 cleanser to dry hands
    rub hands together to spread lather
    wash for 15-20 seconds
    rinse & dry hands thoroughly

  • Inactive ingredients

    AQUA (WATER), GLYCERIN, LAURAMINE OXIDE, BUTYLENE GLYCOL, LACTIC ACID, SALICYLIC ACID, PARFUM (FRAGRANCE), GREEN 5 (CI 61570), YELLOW 5 (CI 19140).

  • PRINCIPAL DISPLAY PANEL

    APP17201-04-R00-Appeal Antibac Hand Wash 1L-V12.jpg

    APP17201-04

    3577410

    appeal

    Antibacterial Hand Wash

    deb

    Made in the USA by Deb

    1 L (33.8 fl oz)

    Distributed exclusively by:

    Interline Brands

    Jacksonville, FL 32207

    www.AppealProducts.com

    R00

  • INGREDIENTS AND APPEARANCE
    APPEAL ANTIBACTERIAL HAND WASH 
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-015
    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)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)  
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11084-015-271000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/12/2017
    2NDC:11084-015-661000 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 not finalpart333A06/12/2017
    Labeler - SC Johnson Professional USA, Inc. (607378015)
    Establishment
    NameAddressID/FEIBusiness Operations
    APEX International, Inc.015226132MANUFACTURE(11084-015)
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

More Info on this Drug

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