Label: DISINFECTANT DEODORANT (WATERFOS)- oystershell, nano silver 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 December 31, 2019

If you are a consumer or patient please visit this version.

  • Active ingredient

    oystershell 20%, nano silver 0.01%

    Purpose

    Disinfectant Deodorant

  • Use

    -For indoors and air: spray the product evenly over the odor causing area, and be careful

    not to slip

    -For clothes: From a distance of 20-40cm, spray evenly on the desired area

    -For wallpaper: From a distance of 30cm, spray evenly to prevent crumpling

  • WARNINGS

    -Although safe to the eyes and skin, upon contact wash with clean water

    -Do not store in direct sunlight or in areas of temperatures in excess of 40 degrees C.

    -Use the product only for intended purposes.

    Keep out of reach of children

    Keep out of reach of children

  • Directions

    For external use only

  • INACTIVE INGREDIENT

    barley stone, zeolite, germanium, ferric chloride, sugar, additive, distilled water

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    DISINFECTANT DEODORANT (WATERFOS) 
    oystershell, nano silver liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71587-0001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OSTREA EDULIS SHELL (UNII: 49OY13BE7Z) (OSTREA EDULIS SHELL - UNII:49OY13BE7Z) OSTREA EDULIS SHELL20 g  in 100 mL
    SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER0.01 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    FERRIC CHLORIDE (UNII: U38V3ZVV3V)  
    GERMANIUM (UNII: 00072J7XWS)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71587-0001-170 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/01/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other06/01/2017
    Labeler - World Sung Ri Co., Ltd (688468543)
    Registrant - World Sung Ri Co., Ltd (688468543)
    Establishment
    NameAddressID/FEIBusiness Operations
    World Sung Ri Co., Ltd688468543manufacture(71587-0001)