Label: DEFENSE AG DISINFECTANT- disinfectant spray spray

  • 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 November 4, 2020

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  • Active Ingredient(s)

    Isopropyl Alcohol 75% v/v. Purpose: Antiseptic to help reduce bacteria that potentially can caused disease.

    Hydrogen Peroxide

  • Inactive ingredients

    ultra pure water, Nano Silver Ag+

  • Use

    To clean and remove allergens, wipe surfaces clean with product and let it dry. Can use on non porous surfaces. Kills 99.99% of germs around the home, office and classroom.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Warnings

    For external use only. Flammable. Keep away from heat or flame

  • Do not use

    • in children less than 2 months of age
    • on open skin wounds
  • Directions

    • Spray enough product to cover all surfaces. Wipe clean and let it dry.
    • Supervise children under 6 years of age when using this product to avoid swallowing.
  • Purpose

    Antisepticbto help reduce bacteria that potentially can cause disease.

  • Package Label - Principal Display Panel

    473 ml NDC: 79930-7115-4

    ISO 16 Oz Label

    946 ml NDC: 79930-7115-6

    ISO 32 Oz Label

    3.79 L NDC: 79930-7115-5

    ISO 32 Oz Label

  • INGREDIENTS AND APPEARANCE
    DEFENSE AG DISINFECTANT 
    disinfectant spray spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79930-7115
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V) HYDROGEN PEROXIDE0.125 mL  in 100 mL
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL75 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    SILVER (UNII: 3M4G523W1G) 0.2 mL  in 100 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79930-7115-4473 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product11/09/2020
    2NDC:79930-7115-6946 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product11/09/2020
    3NDC:79930-7115-53790 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product11/09/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A11/09/2020
    Labeler - Nexderma (079533940)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nexderma079533940manufacture(79930-7115) , pack(79930-7115) , label(79930-7115)
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