Label: NOON FOR KIDS- lutein powder

  • NDC Code(s): 82597-010-01, 82597-010-02
  • Packager: Wholesum Brands Co., Ltd.
  • 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 January 24, 2024

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

  • ACTIVE INGREDIENT

    Lutein 10mg

  • INACTIVE INGREDIENTS

    Carbohydrate, Protein, Fat, Natrium, Refined glucose, Vegetable Cream Mixed Powder, Maple Syrup Powder, Fructooligosaccharide, Blueberry Concentrate Powder, Synthetic flavoring (blueberry), Anhydrous citric acid, vitamin C, Dry yeast (contains selenium), Vitamin and mineral mixture, zinc oxide, Vitamin A mixture, Dry yeast (with vitamin D3), Sicklepod Extract Powder, Bilberry Extract Powder, Beta-carotene mixed formulation, soybean, milk

  • PURPOSE

    Prevent eye diseases

  • WARNINGS

    Excessive intake may temporarily turn the skin yellow. If you have a disease or are taking medication, consult with a doctor, pharmacist, etc. before taking it. If you have an allergic constitution, please check the ingredients before consuming.

  • KEEP OUT OF REACH OF CHILDREN

    Not Applicable

  • Uses

    May help eye health by maintaining the density of macular pigment that can be reduced due to aging.

  • Directions

    Take 1 pouch per day, directly or with water.

  • Other Information

    Do not store this product in an inappropriate place such as high or low temperatures or under direct sun light

  • Questions

    For questions about the product, please contact wholesumbrands@naver.com or call +82-70-7791-0053.

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of cartonImage of carton

  • INGREDIENTS AND APPEARANCE
    NOON FOR KIDS 
    lutein powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82597-010
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Lutein (UNII: X72A60C9MT) (LUTEIN - UNII:X72A60C9MT) Lutein10 mg  in 2 g
    Inactive Ingredients
    Ingredient NameStrength
    Blueberry (UNII: 253RUG1X1A)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    Product Characteristics
    ColoryellowScore    
    ShapeSize
    FlavorBLUEBERRYImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82597-010-0230 in 1 CARTON03/01/2022
    1NDC:82597-010-012 g in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other03/01/2022
    Labeler - Wholesum Brands Co., Ltd. (695260964)
    Registrant - Wholesum Brands Co., Ltd. (695260964)
    Establishment
    NameAddressID/FEIBusiness Operations
    YUYU Health Care Co.,Ltd687171751manufacture(82597-010)