Label: MORNINGCALM V ZERO- zeolite 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 August 10, 2020

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  • Active Ingredient(s)

    zeolite

  • Purpose

    Anti-virus mineral deodorant

  • Use

    Spray Morningcalm V Zero at the place used as
    high as possible for maximum effect (it is effective
    to allow more than 1 second of time to pass ).
    • Spray Morningcalm V Zero on object (mask, clothes,
    shoes, etc.) and dry it to increase the effect

  • Warnings

    Do not use Morningcalm V Zero for any purpose other
    than deodorant. If Morningcalm V Zero is sprayed
    in your face or eyes, wash them with cold water
    immediately.
    • Do not spill Morningcalm V Zero excessively on
    one spot as it may cause slipperiness.
    • Do not use Morningcalm V Zero in areas
    at risk of discoloration or
    bleaching.

  • KEEP OUT OF REACH OF CHILDREN

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

  • Directions

    for external use only

  • INACTIVE INGREDIENT

    Bentonite, Sericite, Sulfur, Molybdate , Calcium , Chitosan, Iodine, Purified water, etc.

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    MORNINGCALM V ZERO 
    zeolite liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78811-0001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZEOLITE A (UNII: Y3NG9WF08W) (ZEOLITE A - UNII:Y3NG9WF08W) ZEOLITE A2.3 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    CALCIUM (UNII: SY7Q814VUP)  
    SODIUM MOLYBDATE DIHYDRATE (UNII: 8F2SXI1704)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    POTASSIUM IODIDE (UNII: 1C4QK22F9J)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78811-0001-1500 mL in 1 BOTTLE; Type 0: Not a Combination Product07/11/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/11/2020
    Labeler - Morningcalmsalt Co., Ltd. (694040871)
    Establishment
    NameAddressID/FEIBusiness Operations
    Morningcalmsalt Co., Ltd.694040871manufacture(78811-0001)