Label: OHTRUST MOUTH AND NASAL RELIEF- hydroxide ions liquid

  • NDC Code(s): 70970-007-01
  • 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 December 14, 2023

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  • Active Ingredient(s)

    Hydroxide ions (544ppm)

  • Purpose

    Anti-bacterial

  • Use

    • For mouth:

    Kills bacteria and virus
    Balance pH
    Instant minty breath

    • For nasal:

    Moisturizes and flushes irritants in nostrils

    Relieves stuffy nose

  • Warnings

    • Avoid contact with eyes. In case of contact, rinse eyes thoroughly with water immediately.
    • Use of this container by more than one person may spread infection.
    • Temporary discomforts such as burning, stinging, sneezing or an increase in nasal discharge may occur.
    • Stop use if rash or irritation develops. Do not drink it!
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children except under adult supervision.

  • Directions

    Spray products 3-4 times directly into the back of the mouth and teeth or into nostril. Allow product to flow down the throat. Repeat when necessary.

  • Other information

    Store below 95˚F (35˚C).

  • Inactive ingredients

    Ultrapure water, Floviva Peppermint Oil (Mentha piperita) (100% Org PPAI)

  • Package Label - Principal Display Panel

    007-0130 mL NDC: 70970-007-01

  • INGREDIENTS AND APPEARANCE
    OHTRUST MOUTH AND NASAL RELIEF 
    hydroxide ions liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70970-007
    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
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70970-007-0130 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product04/28/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other04/28/2022
    Labeler - Nanoplus Life Biomedical Technology Co. Ltd. (657425219)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nanoplus Life Biomedical Technology Co. Ltd.657425219manufacture(70970-007)
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