Label: JIKIMI PHYTONCIDE- titanium dioxide, hypochlorous acid liquid

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

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Drug Label Information

Updated November 13, 2020

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  • ACTIVE INGREDIENT

    Hypochlorous Acid

  • INACTIVE INGREDIENT

    Chamaecyparis Obtusa Leaf Extract, Foeniculum vulgare seed extract, Indican, Maltitol, Pinus Densiflora Leaf Extract, Sorbitol, Water

  • PURPOSE

    • Do not dilute spray.
    • Use at strength for maximum effectiveness.
    • Spray directly, from a distance of about 8 to 10 inches.
    • For equipment or products that are difficult to spray, apply liquid to clean gauze or cotton swab.
  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    Wipe with gauze or cotton swab and let air dry. Spray clothes, equipment, and indoor objects for sterilization and deodorization as required.

  • WARNINGS

    For external use only.

    When using this product

    • Keep out of eyes 
    • In case of contact with eyes, flush thoroughly with water.

    Stop use and ask a doctor if irritation or redness develop and persist for more than 72 hours.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    JIKIMI PHYTONCIDE 
    titanium dioxide, hypochlorous acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71544-0020
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID0.00136 g  in 17 mL
    Inactive Ingredients
    Ingredient NameStrength
    CHAMAECYPARIS OBTUSA LEAF (UNII: 7OL154J5XB)  
    INDICAN (UNII: N187WK1Y1J)  
    MALTITOL (UNII: D65DG142WK)  
    PINUS DENSIFLORA LEAF (UNII: Q1Q9P50WIY)  
    SORBITOL (UNII: 506T60A25R)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71544-0020-117 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product11/09/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/15/2020
    Labeler - MY Corp.,Ltd (688202781)
    Registrant - MY Corp.,Ltd (688202781)
    Establishment
    NameAddressID/FEIBusiness Operations
    MY Corp.,Ltd688202781manufacture(71544-0020) , label(71544-0020) , pack(71544-0020)
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