Label: DEFENDER FOAMING HAND SANITIZER- alcohol 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

    Ethyl Alcohol 62%

  • Purpose

    Antimicrobial

  • Uses

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

    if 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.

  • 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
  • Other Information

    • Store below 110 0F (43 0C)
    • May discolor certain fabrics or surfaces
  • Inactive Ingredients

    Water, DEA-C8-18 Perfluoroalkylethyl Phosphate, Glycerin

  • 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)

  • Product Label

    Product Label

  • INGREDIENTS AND APPEARANCE
    DEFENDER FOAMING HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42953-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    DIETHANOLAMINE BIS(C8-C18 PERFLUOROALKYLETHYL)PHOSPHATE (UNII: 4J55VM509S)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:42953-001-0050 mL in 1 BOTTLE; Type 0: Not a Combination Product10/11/2012
    2NDC:42953-001-01550 mL in 1 BOTTLE; Type 0: Not a Combination Product10/11/2012
    3NDC:42953-001-021000 mL in 1 BOTTLE; 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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