Label: GOLD MATE- hypochlorous acid 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 February 15, 2018

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  • ACTIVE INGREDIENT

    silymarin

  • INACTIVE INGREDIENT

    vitamin B1, vitamin B2, vitamin B6, taurine, soybean lecithin, bee's wax, vitamin C, hovenia dulcis var koreana extract powder, lentinus edodes mycelia extract powder, basidio carp of ganoderma lucium extract powder, dandelion extract powder, nicotinic acid, folic acid


  • PURPOSE

    sterilize and disinfect various pathogenic viruses

    eliminate various bad smell and odor

  • KEEP OUT OF REACH OF CHILDREN

    keep out or reach of the children

  • INDICATIONS & USAGE

    washing and sterilization of hands

    washing and sterilization of fruits, vegetables, and eggs

    sterilization of refrigerators

    sterilization and deodorization of living rooms and bed rooms including floors

  • WARNINGS

    never drink the liquid

    if the liquid gets into the eyes, do not rub eyes but immediately wash with flowing tab water

    if skin is contacted with the undiluted liquid, immediately wash with flowing water

  • DOSAGE & ADMINISTRATION

    for home use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    GOLD MATE 
    hypochlorous acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72115-0001
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID3 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM CATION (UNII: LYR4M0NH37)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72115-0001-1800 mL in 1 BOTTLE; Type 0: Not a Combination Product02/15/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other02/15/2018
    Labeler - DONG-IL GREENSYS CO., LTD. (687989348)
    Registrant - DONG-IL GREENSYS CO., LTD. (687989348)
    Establishment
    NameAddressID/FEIBusiness Operations
    DONG-IL GREENSYS CO., LTD.687989348manufacture(72115-0001)