Label: DEFENDER FOAMING HAND SANITIZER - alcohol liquid 

  • NDC Code(s): 42953-001-00, 42953-001-01, 42953-001-02
  • Packager: Scientific Molecular Technologies
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 10/12

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

  • Drug Facts
  • Active Ingredients

    Ethyl Alcohol 62%

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  • Purpose

    Antimicrobial

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  • Uses

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

    • Flammable. Keep away from fire or flame.
    • 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 or 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.

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  • Directions

    • Place enough product in your palm to thoroughly cover your hands.
    • Rub hands together briskly until dry.
    • Children under 6 years of age should be supervised when using this product
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  • Other Information

    • Store below 1100F (430C)
    • May discolor certain fabrics or surfaces
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  • Inactive Ingredients

    Water, DEA-C8-18 Perfluoroalkylethyl Phosphate, Glycerin

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  • PRINCIPAL DISPLAY PANEL

    DE Fender   SCIENTIFIC MOLECULAR TECHNOLOGIES     Foaming Hand Sanitizer   ELIMINATES 99.999% OF MOST COMMON GERMS THAT CAUSE ILLNESS    NO RINSE MOISTURIZES LEAVES SKIN SOFT     1.7 fl oz (50 ml)

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  • Product Label
  • INGREDIENTS AND APPEARANCE
    DEFENDER FOAMING HAND SANITIZER 
    alcohol liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:42953-001
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALCOHOL (ALCOHOL) ALCOHOL 62 mL  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    DIETHANOLAMINE BIS(C8-C18 PERFLUOROALKYLETHYL)PHOSPHATE  
    GLYCERIN  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:42953-001-00 50 mL in 1 BOTTLE
    2 NDC:42953-001-01 550 mL in 1 BOTTLE
    3 NDC:42953-001-02 1000 mL in 1 BOTTLE
    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(42953-001)
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