Label: DMINE PENTOSE MEDI PLUS- chlorine dioxide 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 July 22, 2020

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  • ACTIVE INGREDIENT

    Chlorine Dioxide

  • PURPOSE

    Hand or space sterilization to effectively reduce disease causing bacteria.

    ■ instant hand sanitization to decrease bacteria on the skin

    ■ Eliminate bacteria through space sterilization to prevent virus infection.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF THE CHILDREN

  • WARNINGS

    ■ Flammable. Keep away from fire or flame.

    ■ For external use only.

    ■ Do not use in eyes.

    ■ lf swallowed, get medical help promptly.

    ■ Stop use, ask doctor lf irritation occurs.

    ■ Keep out of reach of children.

  • DOSAGE & ADMINISTRATION

    for external use only

  • INACTIVE INGREDIENT

    Water, Sodium benzoate, Cellulose, Glycerin, Chamaecyparis obtusa, ext, Chlorine dioxide ion(1-), Minerals

  • INDICATIONS & USAGE

    space sterilization : spray ample amount in area that requires sterilization.

    For external use : apply to clean, dry hands. apply sufficient amount to thoroughly wet all surfaces of hands and fingers. rub onto hands until dry.

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    DMINE PENTOSE MEDI PLUS 
    chlorine dioxide liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79397-0001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLORINE DIOXIDE (UNII: 8061YMS4RM) (CHLORINE DIOXIDE - UNII:8061YMS4RM) CHLORINE DIOXIDE1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    CHAMAECYPARIS OBTUSA LEAF (UNII: 7OL154J5XB)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79397-0001-1500 mL in 1 BOTTLE; Type 0: Not a Combination Product07/22/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/22/2020
    Labeler - DMINE COSMETIC CO., LTD (695714680)
    Registrant - DMINE COSMETIC CO., LTD (695714680)
    Establishment
    NameAddressID/FEIBusiness Operations
    DMINE COSMETIC CO., LTD695714680manufacture(79397-0001)