Label: NANOVER- silver cation spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated October 10, 2020

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  • Active ingredien

    SILVER CATION

  • USE

    Hand or Topical sanitizer to help reduce bacteria that potentially.

  • WHEN USING

    keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

  • Warnings

    Innocuous

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

    Don't put it on your face Hand sterilization and cleaning are possible, but they are not medicines

  • Do not use

    Safe for external or internal use.

    in children less than 2 months of age

    on open skin wounds

  • Stop use and ask doctor

    Stop use and ask doctor irritation or rash occurs. These may be signs of a serious condition.

    If you experience any of the following problems, do not use this product and contact your dermatologist, etc

    In case of abnormalities such as red spots, swelling,itching, irritation, etc. during use

  • PURPOSE

    Antiseptic

  • Keep out of reach of children

    KEEP OUT OF REACH OF CHILDREN

  • Direction

    Spray enough as the need arises on hands, body and surfaces.

  • Other information

    Store between 15-30C (59-86F)

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

    ●Year of manufacture:notation of separate diagram

    ●Expiration day:3years from manufacturing date

    ●Questions or Comments? please call 82-10-6283-4583

  • Inactive ingredient

    Distilled water, Glycine, Methionine

  • label

    80577-301-01

    label

  • INGREDIENTS AND APPEARANCE
    NANOVER 
    silver cation spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80577-301
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SILVER CATION (UNII: 57N7B0K90A) (SILVER CATION - UNII:57N7B0K90A) SILVER CATION0.02 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 99.99 mL  in 100 mL
    METHIONINE (UNII: AE28F7PNPL) 0.01 mL  in 100 mL
    GLYCINE (UNII: TE7660XO1C) 0.07 mL  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80577-301-01100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product10/09/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/09/2020
    Labeler - Korean Algae Association (695504304)
    Registrant - Korean Algae Association (695504304)
    Establishment
    NameAddressID/FEIBusiness Operations
    Dentarow695504328manufacture(80577-301)
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