Label: M.C. (MORNINGCALM) V ZERO- 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 October 6, 2020

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

  • Active Ingredient(s)

    chlorine dioxide

  • 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

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  • INGREDIENTS AND APPEARANCE
    M.C. (MORNINGCALM) V ZERO 
    chlorine dioxide liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78811-0002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLORINE DIOXIDE (UNII: 8061YMS4RM) (CHLORINE DIOXIDE - UNII:8061YMS4RM) CHLORINE DIOXIDE0.3 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78811-0002-13785.412 mL in 1 CONTAINER; Type 0: Not a Combination Product10/07/2020
    2NDC:78811-0002-27570.824 mL in 1 CONTAINER; Type 0: Not a Combination Product10/07/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/07/2020
    Labeler - Morningcalmsalt Co., Ltd. (694040871)
    Establishment
    NameAddressID/FEIBusiness Operations
    Morningcalmsalt Co., Ltd.694040871manufacture(78811-0002)