Label: CLARITYING TURN OVER RICE PERFECT OIL FOAM CLEANSER (oryza sativa- rice bran oil liquid

  • NDC Code(s): 71217-0064-1, 71217-0064-2
  • Packager: inthismorning co ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated February 1, 2023

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  • ACTIVE INGREDIENT

    rice bran oil

  • INACTIVE INGREDIENT

    Water, Glycerin, etc

  • PURPOSE

    to remove makeup quickly and easily without having no cleanse twice

  • KEEP OUT OF REACH OF CHILDREN

    keep out or reach of the children

  • INDICATIONS & USAGE

    before use, shake to mix the layers and pump a suitable amount onto wet hands,

    massage to cleanse makeup and rinse thoroughly with warm water

  • WARNINGS

    This product is for exeternal use only. Do not use for internal use
    Storage and handling precautions
    If possible, avoid direct sunlight and store in cool and area of low humidity in order to maintain the quality of the product and avoid misuse
    Avoid placing the product near fire and store out in reach of children

    - consult a physician in case of abnormal symptoms, such as red spots, swelling or itching, or side effects in the areas of application due to direct light during or after using the product

    - do not use on wounded area

  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    CLARITYING TURN OVER RICE PERFECT OIL FOAM CLEANSER 
    oryza sativa (rice) bran oil liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71217-0064
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RICE BRAN OIL (UNII: LZO6K1506A) (RICE BRAN OIL - UNII:LZO6K1506A) RICE BRAN OIL0.01 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71217-0064-1150 mL in 1 BOTTLE; Type 0: Not a Combination Product01/15/2023
    2NDC:71217-0064-230 mL in 1 BOTTLE; Type 0: Not a Combination Product01/15/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/15/2023
    Labeler - inthismorning co ltd (695126076)
    Registrant - inthismorning co ltd (695126076)
    Establishment
    NameAddressID/FEIBusiness Operations
    EVERCOS CO. LTD.688318260manufacture(71217-0064)
    Establishment
    NameAddressID/FEIBusiness Operations
    inthismorning co ltd695126076label(71217-0064)
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