Label: MAXCLINIC DEEP AND DEEPER MESO CHANGE AMPOULE- niacinamide, adenosine liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 69058-500-01, 69058-500-02 - Packager: N&B LAB.Co.Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated March 14, 2017
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- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive Ingredients: Centella Asiatica Leaf Water, Glycerin, Caprylic/Capric Triglyceride, Hydrogenated Lecithin, Propanediol, Olea Europaea (Olive) Fruit Oil, 1,2-Hexanediol, Ethylhexyl Palmitate, Squalane, Collagen, Glyceryl Stearate SE, Potassium Cetyl Phosphate, Helianthus Annuus (Sunflower) Seed Oil, Polyglyceryl-3 Cetyl Ether, Triolein, Glyceryl Dioleate, Sodium Hyaluronate, Hydrolyzed Hyaluronic Acid, Ceramide NP, Ceramide NS, Ceramide EOP, Ceramide AP, Polyglyceryl-10 Myristate, Polyglyceryl-10 Laurate, Tocopheryl Acetate, Allantoin, Panthenol, Argania Spinosa Kernel Oil, Simmondsia Chinensis (Jojoba) Seed Oil, Sodium Ascorbyl Phosphate, Gossypium Herbaceum (Cotton) Seed Oil, Arctium Lappa Seed Oil, Pyridoxine HCl, Cyanocobalamin, Maltodextrin, Citric Acid, Sodium Citrate
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Directions
- DOSAGE & ADMINISTRATION
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MAXCLINIC DEEP AND DEEPER MESO CHANGE AMPOULE
niacinamide, adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69058-500 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 0.14 g in 7 mL Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.002 g in 7 mL Inactive Ingredients Ingredient Name Strength Glycerin (UNII: PDC6A3C0OX) Propanediol (UNII: 5965N8W85T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69058-500-02 4 in 1 CARTON 12/20/2016 1 NDC:69058-500-01 7 mL in 1 VIAL; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/20/2016 Labeler - N&B LAB.Co.Ltd (690332858) Registrant - N&B LAB.Co.Ltd (690332858) Establishment Name Address ID/FEI Business Operations N&B LAB.Co.Ltd 690332858 manufacture(69058-500)