Label: PURE CELL THERAPY- niacinamide, adenosine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 73651-010-01, 73651-010-02 - Packager: NY Beast
- 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 March 16, 2020
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients:
Water, Cyclopentasiloxane, Butylene glycol, Glycerin, Squalane, Betaine, Limnanthes Alba (Meadowfoam) Seed Oil, Glyceryl Stearate, Octyldodecyl Myristate, Phytosteryl Isostearyl Dimer Dilinoleate, PEG-40 Stearate, Stearic Acid, Phytosteryl/Behenyl/Octyldodecyl Lauroyl Glutamate, Persea Gratissima (Avocado) Oil, Jojoba Esters, PEG-100 Stearate, Polyacrylate-13, Mangifera Indica (Mango) Seed Butter, Human Cord Blood Stem Cell Conditioned Media, Helianthus Annuus (Sunflower) Seed Oil, Hexadecane, Cetyl PEG/PPG-10/1 Dimethicone, Panthenol, PEG-30 Dipolyhydroxystearate, Tetradecane, Dipropylene Glycol, Hydroxyacetophenone, Dimethicone, Hydrogenated Vegetable Oil, Polyisobutene, 1,2-Hexanediol, Cetearyl Alcohol, Tocopherol, Dodecane, Caprylyl Glycol, Polyquaternium-51, Octadecane, Copernicia Cerifera (Carnauba) Wax, Tocopheryl Linoleate, Dimethiconol, Stearyl Alcohol, Ethylhexylglycerin, Eicosane, Polysorbate 20, Lauryl PEG/PPG-18/18 Methicone, Sorbitan Isostearate, Beta-Glucan, Hyaluronic Acid, Phenoxyethanol, Disodium EDTA, Myristyl Alcohol, Dodecene, Lauryl Alcohol, Isostearyl Alcohol, Dipotassium Glycyrrhizate, Isopropyl Alcohol - PURPOSE
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WARNINGS
Warnings:
For external use only. Not for internal use.
Avoid contact with eyes. If contact with the eyes occurs, wash out thoroughly with water. Discontinue use if signs of irritation or rashes appear. If the symptoms are severe, stop using, and seek medical advice immediately. Keep out of reach of children. - KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- QUESTIONS
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PURE CELL THERAPY
niacinamide, adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73651-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 1.0 g in 50 mL Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.02 g in 50 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Butylene glycol (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73651-010-02 1 in 1 CARTON 02/01/2020 1 NDC:73651-010-01 50 mL in 1 CONTAINER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 02/01/2020 Labeler - NY Beast (695626250) Registrant - NY Beast (695626250) Establishment Name Address ID/FEI Business Operations Soleo Cosmetic Co., Ltd. 557829412 manufacture(73651-010)
