Label: EVECODE ECO-FRIENDLY SAFE SANITIZERSPRAY- calcium 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 March 24, 2020

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  • ACTIVE INGREDIENT

    calcium oxide

  • INACTIVE INGREDIENT

    water

  • PURPOSE

    Safe Sterilizer Spray

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF THE CHILDREN

  • INDICATIONS & USAGE

    Spray it on the object and space where sterilization and disinfection is required, and then dry it naturally or wipe it off with a dry cloth or tissue.

  • WARNINGS

    For external use only.

    Flammable, keep away from fire or flame.

    Store at room temperature, away from high temperatures and direct sunlight. Do not mix with water or other chemicals. Keep this product out of the reach of children. Please do not use for other purposes.

    Emergency treatment : In case of accidental drinking, drink plenty of water. If it gets into your eyes, wash with running water and consult a doctor if there is any problem.

  • DOSAGE & ADMINISTRATION

    Spray it on the hands and object and space where sterilization and disinfection is required, and then dry it naturally or wipe it off with a dry cloth or tissue.

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    EVECODE ECO-FRIENDLY SAFE SANITIZERSPRAY 
    calcium dioxide liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73772-0001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIME (CALCIUM OXIDE) (UNII: C7X2M0VVNH) (LIME (CALCIUM OXIDE) - UNII:C7X2M0VVNH) LIME (CALCIUM OXIDE)20 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73772-0001-2300 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product03/21/2020
    2NDC:73772-0001-380 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product03/21/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other03/21/2020
    Labeler - MEDINCOZ INC. (694771137)
    Registrant - MEDINCOZ INC. (694771137)
    Establishment
    NameAddressID/FEIBusiness Operations
    MEDINCOZ INC.694771137manufacture(73772-0001) , label(73772-0001)