Label: OHTRUST NANO ION WATER- hydroxide ions liquid

  • 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 January 13, 2022

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  • Active Ingredient(s)

    Hydroxide Ions (544 ppm) Purpose: Antimicrobial

  • Purpose

    Purpose: Antimicrobial

  • Use

    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

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

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

  • WHEN USING

    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

    Keep out of reach of children

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

  • Directions

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

  • Other information

    Store at room temperature

  • Inactive ingredients

    Pure Water 99.9%

  • Package Label - Principal Display Panel

    Front LabelDrug Facts60000 mg NDC: 78218-007-01

  • INGREDIENTS AND APPEARANCE
    OHTRUST NANO ION WATER 
    hydroxide ions liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78218-007
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROXIDE ION (UNII: 9159UV381P) (HYDROXIDE ION - UNII:9159UV381P) HYDROXIDE ION0.0544 mg  in 100 mg
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78218-007-0160000 mg in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product12/14/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other12/14/2020
    Labeler - Kunshan Nano Environmental Protection Technology Co. Ltd. (560346395)
    Establishment
    NameAddressID/FEIBusiness Operations
    Kunshan Nano Environmental Protection Technology Co. Ltd.560346395manufacture(78218-007)