Label: VITAPLUS ECO HYGIENE- 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 May 10, 2021

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

  • ACTIVE INGREDIENT

    hypochlorous acid

  • INACTIVE INGREDIENT

    Foeniculum vulgare seed extract, Indican, Maltitol, Sorbitol, Water

  • PURPOSE

    Antiseptic

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    Do not dilute.• Use at strength for maximum effectiveness.• For equipment or products that are difficult to spray, apply liquid to clean gauze or cotton swab.

  • WARNINGS

    Warnings

    For external use only.

    When using this product • Keep out of eyes • In case of contact with eyes, flush thoroughly with water.

    Stop use and ask a doctor ifirritation or redness develop and persist for more than 72 hours.

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

  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    VITAPLUS ECO HYGIENE 
    hypochlorous acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71544-0025
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID0.008 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    INDICAN (UNII: N187WK1Y1J)  
    SORBITOL (UNII: 506T60A25R)  
    MALTITOL (UNII: D65DG142WK)  
    WATER (UNII: 059QF0KO0R)  
    FENNEL SEED (UNII: G3QC02NIE6)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71544-0025-14000 mL in 1 DRUM; Type 0: Not a Combination Product04/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other04/01/2021
    Labeler - MY Corp.,Ltd (688202781)
    Registrant - MY Corp.,Ltd (688202781)
    Establishment
    NameAddressID/FEIBusiness Operations
    MY Corp.,Ltd688202781manufacture(71544-0025) , label(71544-0025) , pack(71544-0025)