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DEFENDER Antiseptic Foam Hand Sanitizer Alcohol-Free (Scientific Molecular Technologies)

Available Formats

Dosage Form Package Information Links
LIQUID 50 mL in 1 BOTTLE, PUMP (42953-002-00) Label Information
LIQUID 1000 mL in 1 BOTTLE, PUMP (42953-002-02) Label Information
LIQUID 550 mL in 1 BOTTLE, PUMP (42953-002-01) Label Information

Complete DEFENDER Antiseptic Foam Hand Sanitizer Alcohol-Free Information

  • 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

    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 Type HUMAN OTC DRUG Item Code (Source) NDC:42953-002
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    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 Code Package Description Marketing Start Date Marketing End Date
    1 NDC:42953-002-00 50 mL in 1 BOTTLE, PUMP
    2 NDC:42953-002-01 550 mL in 1 BOTTLE, PUMP
    3 NDC:42953-002-02 1000 mL in 1 BOTTLE, PUMP
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part333E 10/11/2012
    Labeler - Scientific Molecular Technologies (028159474)
    Establishment
    Name Address ID/FEI Business Operations
    Artemis Bio-Solutions Inc. 963442541 manufacture(42953-002)