Label: OHTRUST NANO ION WATER- hydroxide ions liquid

  • NDC Code(s): 70970-006-01, 70970-006-02, 70970-006-03, 70970-006-04, view more
    70970-006-05
  • Packager: Nanoplus Life Biomedical Technology Co. Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated January 5, 2024

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  • Active Ingredient(s)

    Hydroxide ions (544ppm)

  • Purpose

    Anti-bacterial, Anti-viral

  • 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

  • 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

    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

    60 ml label60 mL NDC: 70970-006-01

    1000 ml label1000 mL NDC: 70970-006-02

    5000 ml label5000 mL NDC: 70970-006-03

    20000 ml label20000 mL NDC: 70970-006-04

    drug facts label

  • INGREDIENTS AND APPEARANCE
    OHTRUST NANO ION WATER 
    hydroxide ions liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70970-006
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROXIDE ION (UNII: 9159UV381P) (HYDROXIDE ION - UNII:9159UV381P) HYDROXIDE ION0.2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70970-006-0160 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product11/23/2020
    2NDC:70970-006-021000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product11/23/2020
    3NDC:70970-006-035000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/23/2020
    4NDC:70970-006-0420000 mL in 1 PAIL; Type 0: Not a Combination Product11/23/2020
    5NDC:70970-006-051000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/23/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other11/23/2020
    Labeler - Nanoplus Life Biomedical Technology Co. Ltd. (657425219)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nanoplus Life Biomedical Technology Co. Ltd.657425219manufacture(70970-006)
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