Label: DR.JUCRE REBIRTH WHITE- niacinamide emulsion
- NDC Code(s): 83071-030-01, 83071-030-02
- 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
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INACTIVE INGREDIENTS
Water, Glycerin, Butylene Glycol, Dimethicone, Cyclopentasiloxane, Cetyl Ethylhexanoate, Cyclohexasiloxane, Butyrospermum Parkii (Shea) Butter, Human Adipose Derived Stem Cell Conditioned Media, Pentylene Glycol, Hydrogenated Vegetable Oil, Polyglyceryl-3 Methylglucose Distearate, Betaine, Glyceryl Stearate, Stearyl Alcohol, Cetyl Alcohol, Chondrus Crispus Extract, Caprylyl Glycol, Sorbitan Stearate, Phenoxyethanol, PEG-100 Stearate, Saccharum Officinarum (Sugarcane) Extract, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Beeswax, Carbomer, Triethanolamine, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Isohexadecane, Citrus Grandis (Grapefruit) Peel Oil, Sodium Phytate, Xanthan Gum, 1,2-Hexanediol, Polysorbate 80, Sorbitan Oleate, Cynanchum Atratum Extract, Dimethicone/Vinyl Dimethicone Crosspolymer, Myristyl Alcohol, Lauryl Alcohol, Althaea Rosea Flower Extract, Ethylhexylglycerin, Plankton Extract, Hydroxypropyl Cyclodextrin, Thioctic Acid, Tremella Fuciformis (Mushroom) Extract, Potassium Hydroxide
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- Other Information
- Questions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DR.JUCRE REBIRTH WHITE
niacinamide emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83071-030 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 2.0 g in 100 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) Butylene Glycol (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83071-030-02 1 in 1 CARTON 10/01/2022 1 NDC:83071-030-01 120 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/01/2022 Labeler - NATURECELL CO., LTD. (689282572) Registrant - NATURECELL CO., LTD. (689282572) Establishment Name Address ID/FEI Business Operations Cosmax, Inc. 689049693 manufacture(83071-030)