Label: DEFENSE AG- defense ag hand sanitizing gel gel

  • 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 July 21, 2020

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

  • Active Ingredient

    Ethyl Alcohol 80% - Antiseptic to help reduce bacteria that potentialy can cause disease.

  • Inactive Ingredients

    Glycerol

    Carbomer

    Ultra Pure Water

  • Uses

    Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available. Apply Defense Ag on hands rubbing together until dried. Repeat as often as necessary.

  • KEEP OUT OF REACH OF CHILDREN

    Adult super vision recommended for children under 6 years old.

  • WARNINGS

    Keep away from fire and flame.

    Flammable.

    For external use on hands only.

    Keep out of eyes, ears and mouth.

    If contact in eyes, flush thoroughly with water.

    Keep out of reach of children.

    If swallowed seek medical help immediately or call your poison control center.

    Store between 15-30C (58-86F).

    Avoid freezing and excessive heat above 40C( 104F).

    will damage wood finishes, plastics and some fabrics.

  • DO NOT USE

    Children less than 2 months of age or on open wounds.

  • DOSAGE & ADMINISTRATION

    Dosage: upto 10 times a day

    Place enough product on hands to cover all surfaces. Rub hands together until dry.

    Administration: Topical

  • PURPOSE

    Purpose: To help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

  • Nexderma Defense Ag

    4oz label 16oz label

  • INGREDIENTS AND APPEARANCE
    DEFENSE AG 
    defense ag hand sanitizing gel gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79930-7101
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL80 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    CARBOMER 940 (UNII: 4Q93RCW27E) 0.25 mL  in 100 mL
    WATER (UNII: 059QF0KO0R) 10 mL  in 100 mL
    GLYCERIN (UNII: PDC6A3C0OX) 1 mL  in 100 mL
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79930-7101-1100 mL in 1 BOTTLE; Type 0: Not a Combination Product09/30/2020
    2NDC:79930-7101-4500 mL in 1 BOTTLE; Type 0: Not a Combination Product09/30/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A09/30/2020
    Labeler - Nederma Inc (079533940)