Label: DEFENDER ANTISEPTIC FOAM HAND- benzalkonium chloride soap

  • 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 June 1, 2021

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

View All Sections
  • Drug Facts


  • Active Ingredients

    Benzalkonium Chloride 0.13%

  • Purpose

    Antimicrobial

  • Uses

    • For hand washing to decrease bacteria on the skin.
    • Recommended for repeated use.
  • Warnings

    • For external use only.

    When using this product

    avoid contact with eyes. In case of eye contact, flush eyes with water.

    Stop use and ask a doctor

    irritation or redness develops. If 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

    • Pump a small amount of foam into palm of hand.
    • Run thoroughly over all surfaces of both hands for 15 seconds
    • Rinse with potable water.
  • Inactive Ingredients

    Water, (aqua), butylene glycol,  Dihydroxypropyl PEG-5 linoleammonium chloride, Dihydroxyethyl cocamine oxide, glycereth-2 cocoate, Hydroxypropyl methylcellulose.

  • PRINCIPAL DISPLAY PANEL

    DE Fender  SCIENTIFIC MOLECULAR TECHNOLOGIES    ANTISEPTIC FOAM  Hand Soap    ELIMINATES 99.999% OF MOST COMMON GERMS THAT CAUSES ILLNESS   NO RINSE MOISTURIZES LEAVES SKIN SOFT  8.4 fl oz (250 ml)

  • Product Label

    Product Label

  • INGREDIENTS AND APPEARANCE
    DEFENDER ANTISEPTIC FOAM HAND 
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42953-000
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)  
    DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)  
    GLYCERETH-2 COCOATE (UNII: JWM00VS7HC)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:42953-000-00250 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/11/2012
    2NDC:42953-000-011000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/11/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E10/11/2012
    Labeler - Scientific Molecular Technologies (028159474)
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!