Label: DR.JUCRE REBIRTH WHITE EYE- niacinamide cream

  • NDC Code(s): 83071-040-01, 83071-040-02
  • Packager: NATURECELL 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 November 7, 2022

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

  • ACTIVE INGREDIENTS

    Niacinamide 2.0%
    Adenosine 0.04%

  • INACTIVE INGREDIENTS

    Water, Human Adipose Derived Stem Cell Conditioned Media, Cyclopentasiloxane, Butylene Glycol, Glycerin, Cyclohexasiloxane, PEG-240/HDI Copolymer Bis-Decyltetradeceth-20 Ether, Pentylene Glycol, Polysorbate 20, Dimethicone, Phenoxyethanol, Sodium Polyacrylate, Dimethiconol, Dimethicone/Vinyl Dimethicone Crosspolymer, Carbomer, Tromethamine, Disodium EDTA, PVM/MA Copolymer, Potassium Laurate, BHT, Hydroxypropyl Cyclodextrin, Thioctic Acid, 1,2-Hexanediol, Plankton Extract, Tremella Fuciformis (Mushroom) Extract, Potassium Hydroxide

  • PURPOSE

    Skin Brightening
    Anti wrinkle

  • WARNINGS

    For external use only.
    Avoid contact with eyes.
    Discontinue use if signs of irritation or rashes appear.
    Replace the cap after use.
    Refrain from using it on wounded areas.
    Keep out of reach of children.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of the reach of children.

  • Uses

    ■ Helps brighten skin tone
    ■ Helps improve wrinkle problem

  • Directions

    ■ Apply an appropriate amount evenly on the skin.

  • Other Information

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

  • Questions

    ■ www.ibiostar.com
    ■ Tel (424)227-9568

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    DR.JUCRE REBIRTH WHITE EYE 
    niacinamide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83071-040
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide2.0 g  in 100 mL
    Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine0.04 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    Butylene Glycol (UNII: 3XUS85K0RA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83071-040-021 in 1 CARTON10/01/2022
    1NDC:83071-040-0130 mL in 1 CONTAINER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/01/2022
    Labeler - NATURECELL CO., LTD. (689282572)
    Registrant - NATURECELL CO., LTD. (689282572)
    Establishment
    NameAddressID/FEIBusiness Operations
    Cosmax, Inc.689049693manufacture(83071-040)