Label: QUEENS ROSE RECOVERY- niacinamide, adenosine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 71252-050-01, 71252-050-02 - Packager: Cdpharmtec Co.,ltd
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated March 24, 2017
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- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients: Rosa Damascena Flower Water, Water, Glycerin, Butylene Glycol, Dipropylene Glycol, Propanediol, Cyclopentasiloxane, 1,2-Hexanediol, Trehalose, Polysorbate 20, Cyclohexasiloxane, Dimethicone/Vinyl Dimethicone Crosspolymer, Dimethicone, Squalane, Carbomer, Potassium Hydroxide, Polyacrylate-13, Ceramide NP, Human Adipocyte Conditioned Media Extract, Xanthan Gum, Polyisobutene, Fragrance, Fructooligosaccharides, Saccharide Hydrolysate, Phospholipids, Ethylhexylglycerin, Pullulan, Phytosphingosine, Caprylyl Glycol, Sorbitan Isostearate, Disodium EDTA, Phytosterols, Sodium Hyaluronate, Gardenia Florida Fruit Extract, Vaccinium Myrtillus Fruit/Leaf Extract, Dextrin, Saccharum Officinarum (Sugar Cane) Extract, Tropolone, Citrus Limon (Lemon) Fruit Extract, Citrus Aurantium Dulcis(Orange) Fruit Extract, Acer Saccharium (Sugar Maple) Extract, Prunus Mume Fruit Extract, Nelumbo Nucifera Flower Extract, Chondrus Crispus(Carrageenan) Extract, Olea Europaea (Olive) Fruit Oil, Lecithin, Propylene Glycol, Hydrolyzed Pea Protein, Butyrospermum Parkii(Shea Butter), Citric Acid
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
QUEENS ROSE RECOVERY
niacinamide, adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71252-050 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 1.2 g in 60 g Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.024 g in 60 g Inactive Ingredients Ingredient Name Strength ROSA DAMASCENA FLOWER OIL (UNII: 18920M3T13) Water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71252-050-02 1 in 1 CARTON 03/02/2017 1 NDC:71252-050-01 60 g 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 03/02/2017 Labeler - Cdpharmtec Co.,ltd (694209262) Registrant - Cdpharmtec Co.,ltd (694209262) Establishment Name Address ID/FEI Business Operations Cdpharmtec Co.,ltd 694209262 relabel(71252-050) Establishment Name Address ID/FEI Business Operations COSON Co., Ltd._Osan Plant 689847210 manufacture(71252-050)