Label: DR.JUCRE REBIRTH WHITE BB- titanium dioxide, octinoxate, zinc oxide, niacinamide, adenosine cream

  • NDC Code(s): 83071-070-01, 83071-070-02
  • Packager: NATURECELL CO., LTD.
  • Category: HUMAN OTC DRUG LABEL

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 8, 2022

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  • ACTIVE INGREDIENTS

    Titanium Dioxide 12.11%
    Ethylhexyl Methoxycinnamate 5.00%
    Zinc Oxide 2.93%
    Niacinamide 2.0%
    Adenosine 0.04%

  • INACTIVE INGREDIENTS

    Water, Cyclopentasiloxane, Phenyl Trimethicone, Glycerin, Butylene Glycol Dicaprylate/Dicaprate, PEG-10 Dimethicone, Zinc Oxide (CI 77947), 1,2-Hexanediol, Tridecyl Trimellitate, Disteardimonium Hectorite, Mica (CI 77019), Iron Oxides (CI 77492), Trimethylsiloxysilicate, Cetyl PEG/PPG-10/1 Dimethicone, Human Adipose Derived Stem Cell Conditioned Media, Silica, Isododecane, Magnesium Sulfate, Dimethicone/Vinyl Dimethicone Crosspolymer, Cetyl Dimethicone, Dimethicone, Iron Oxides (CI 77491), Aluminum Hydroxide, Potassium Sorbate, Triethoxycaprylylsilane, Stearic Acid, Iron Oxides (CI 77499), Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Trisodium Ethylenediamine Disuccinate, Xanthan Gum, Hydrogenated Castor Oil Isostearate, Citrus Grandis (Grapefruit) Peel Oil, Tin Oxide (CI 77861), Hydrolyzed Hyaluronic Acid, Plukenetia Volubilis Seed Oil, Totarol, Butylene Glycol, Adansonia Digitata Pulp Extract, Hydrolyzed Algin, Cucumis Melo (Melon) Fruit Extract, Viscum Album (Mistletoe) Leaf Extract, Sodium Benzoate, BHT

  • PURPOSE

    Sunscreen
    Sunscreen
    Sunscreen
    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 prevent sun burn
    ■ Helps brighten skin tone
    ■ Helps improve wrinkle problem

  • Directions

    ■ Apply an appropriate amount evenly on the skin.
    ■ Apply liberally and uniformly to all exposed areas 15-20 minutes before sun exposure. Reapply often (every 2 hours) and after swimming, excessive perspiration and washing to ensure maximum sun protection.

  • 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 BB 
    titanium dioxide, octinoxate, zinc oxide, niacinamide, adenosine cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83071-070
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Titanium Dioxide (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) Titanium Dioxide12.11 g  in 100 mL
    Octinoxate (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) Octinoxate5.00 g  in 100 mL
    Zinc Oxide (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION2.93 g  in 100 mL
    NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE2.00 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)  
    Phenyl Trimethicone (UNII: DR0K5NOJ4R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83071-070-021 in 1 CARTON10/01/2022
    1NDC:83071-070-0130 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(83071-070)