Label: CURITHYS- sodium hyaluronate patch

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated December 1, 2021

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  • ACTIVE INGREDIENT

    Sodium hyaluronate

  • INACTIVE INGREDIENT

    Niacinamide
    Salicylic Acid
    Sh-Oligopepide-1
    Sh-Polypepide-1
    TetraPeptide-44
    Centella Asiatica Extract
    Tranexamic acid
    Camellia Japonica Flower Extract

  • PURPOSE

    Micro-pyramid stimulates the skin and gives moisture and nutrition to sensitive skin.

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    Remove the protective film from the patch.

    Attach it vertically to the desired site.

    Re-press on thea ttached patch every few minutes..

    Remove the patch after attaching for more than 1 hour.

  • WARNINGS

    Use it for your own use only.

    For external use only.

    Discontinue use if adverse reaction occurs.

    Contact a physician if symptoms persist.

    Store at room temperature

    .Do not reuse it as a disposable product.

    Please use it immediately after opening.

  • DOSAGE & ADMINISTRATION

    for topical use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    CURITHYS 
    sodium hyaluronate patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72945-0002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONATE SODIUM94.39 mg  in 100 mg
    Inactive Ingredients
    Ingredient NameStrength
    NIACINAMIDE (UNII: 25X51I8RD4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72945-0002-26 in 1 POUCH07/21/2019
    1NDC:72945-0002-15 mg in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/21/2019
    Labeler - J World (690082781)
    Registrant - J World (690082781)
    Establishment
    NameAddressID/FEIBusiness Operations
    J World690082781label(72945-0002) , manufacture(72945-0002)
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