Label: DR.JUCRE REBIRTH ACTIVATING TONER- betaine liquid

  • NDC Code(s): 83071-020-01, 83071-020-02
  • Packager: NATURECELL CO., LTD.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated November 7, 2022

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  • ACTIVE INGREDIENTS

    Betaine 0.001%

  • INACTIVE INGREDIENTS

    Water, Triethylhexanoin, Glycerin, Hydrogenated Poly(C6-14 Olefin), Butylene Glycol, Human Adipose Derived Stem Cell Conditioned Media, Pentylene Glycol, Alcohol Denat., Steareth-2, Phenoxyethanol, Hydrogenated Lecithin, Algin, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Citrus Grandis (Grapefruit) Peel Oil, Plankton Extract, Hydroxypropyl Cyclodextrin, Thioctic Acid, 1,2-Hexanediol, Tremella Fuciformis (Mushroom) Extract, Potassium Hydroxide

  • PURPOSE

    Skin Protectant

  • 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

    ■ skin protectant

  • 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 ACTIVATING TONER 
    betaine liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83071-020
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Betaine (UNII: 3SCV180C9W) (BETAINE - UNII:3SCV180C9W) Betaine0.001 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Triethylhexanoin (UNII: 7K3W1BIU6K)  
    Glycerin (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83071-020-021 in 1 CARTON10/01/2022
    1NDC:83071-020-01150 mL in 1 BOTTLE; 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(83071-020)
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