Label: DEFENDER ANTISEPTIC FOAM HAND SANITIZER ALCOHOL-FREE- benzalkonium chloride liquid

  • 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 June 1, 2021

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  • Drug Facts


  • Active Ingredients

    Benzalkonium Chloride 0.13%

  • Purpose

    Antimicrobial

  • Uses

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

    • For external use only.

    Do not use in eyes

    if contact occurs, flush eyes with water.

    Stop use and ask a doctor

    if irritation or redness develops. If condition persists for more than 72 hours, consult a doctor.

    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.
    • Wet hands thoroughly with product and allow to dry without wiping.
    • Rub hands together briskly until dry.
  • Inactive Ingredients

    Water, dihydroxypropyl PEG-5 linoleammonium chloride, glycereth-2 cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide, fragrance

  • PRINCIPAL DISPLAY PANEL

    DE Fender  SCIENTIFIC MOLECULAR TECHNOLOGIES    ANTISEPTIC FOAM  Hand Sanitizer  ALCOHOL-FREE    ELIMINATES 99.999% OF MOST COMMON GERMS THAT CAUSES ILLNESS   NO RINSE MOISTURIZES LEAVES SKIN SOFT   EFFECTIVE AGAINST STAPH, MRSA, VRE, NOROVIRUS   1.7 fl oz (50 ml)

  • Product Label

    Product Label

  • INGREDIENTS AND APPEARANCE
    DEFENDER ANTISEPTIC FOAM HAND SANITIZER ALCOHOL-FREE 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42953-002
    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)  
    DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)  
    GLYCERETH-2 COCOATE (UNII: JWM00VS7HC)  
    BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)  
    DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:42953-002-0050 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/11/2012
    2NDC:42953-002-01550 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/11/2012
    3NDC:42953-002-021000 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 finalpart333A10/11/2012
    Labeler - Scientific Molecular Technologies (028159474)
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