Label: OHTRUST NANO ION WATER- potassium hydroxide liquid

  • NDC Code(s): 70970-100-01, 70970-100-02
  • Packager: Nanoplus Limited (Cayman) Taiwan Branch
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated September 26, 2016

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  • Active Ingredients

    Potassium hydroxide (0.2%)

  • Purpose

    Antimicrobial

  • Keep out of reach of children

     Do not swallow. In case of accidental ingestion, seek professional assistance.

  • Uses

    Sanitizer to help decrease bacteria. Hygienic disinfectant especially suited for sanitizing hands, skin, or the surface that it needs.

  • Warnings

    For external use only
     Cannot drink
    Do not use when liquid comes in contact with eyes, rinse immediately with water and consult the doctor.
    When using this product
     Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

    Store at room temperature

  • Inactive Ingredients

    Nano-ion water, Gel, Small clustered floral water

  • Directions

    Spray on hands, skin, or places that need to be antibacterial. After spray, let it dry and no need to rinse.

  • OHTrust Nano Ion Water

    nano water

  • INGREDIENTS AND APPEARANCE
    OHTRUST NANO ION WATER 
    potassium hydroxide liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70970-100
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Potassium hydroxide (UNII: WZH3C48M4T) (HYDROXIDE ION - UNII:9159UV381P) Potassium hydroxide0.2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    water (UNII: 059QF0KO0R)  
    GELATIN, UNSPECIFIED (UNII: 2G86QN327L)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70970-100-021 in 1 PACKAGE09/26/2016
    1NDC:70970-100-01100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/26/2016
    Labeler - Nanoplus Limited (Cayman) Taiwan Branch (656283417)
    Registrant - Nanoplus Limited (Cayman) Taiwan Branch (656283417)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nanoplus Limited (Cayman) Taiwan Branch656283417manufacture(70970-100)