Label: DARYOMI STEMCELL LIFT EYE PREMIUM- adenosine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 90034-010-01, 90034-010-02 - Packager: The Partners Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated October 15, 2020
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENTS
Annona Muricata Leaf Extract, Glycerin, Propylen Glycol, Glyceryl Stearate, Sodium Hyaluronate, Butylene Glycol, Castanea Crenata Shell Extract, Hydrolyzed Collagen, Centella Asiatica Extract, Triethanolamine, PEG-60 Hydrogenated Castor Oil, Dipalmitoyl Hydroxyproline, Chlorphenesin, Glycyrrhiza Glabra (Licorice) Root Extract, Camellia Sinensis Leaf Extract, Portulaca Oleracea Extract, Linum Usitatissimum (Linseed) Seed Extract, Hibiscus Esculentus Fruit Extract, Aloe Barbadensis Leaf Juice, Arctium Lappa Root Extract, Hibiscus Mutabilis Flower Extract, Corchorus Olitorius Leaf Extract, Fragrance, CI 77491, Magnesium Aluminum Silicate, Xanthan Gum, Lysine HCL, Proline, Sodium Ascorbyl Phosphate, Acetyl Methionine, Theanine, Panthenol, Acetyl Hexapeptide-8, Dipeptide Diaminobutyroyl Benzylamide Diacetate, Carbomer, Disodium EDTA, Allantoin, Lecithin, Olea Europaea (Olive) Fruit Oil, Phytosterols, Squalane, Butyrospermum Parkii (Shea Butter), Ceramide 3, Propanediol
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DARYOMI STEMCELL LIFT EYE PREMIUM
adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:90034-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.004 g in 10 mL Inactive Ingredients Ingredient Name Strength Glycerin (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:90034-010-02 2 in 1 CARTON 10/01/2020 1 NDC:90034-010-01 10 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 10/01/2020 Labeler - The Partners Co., Ltd. (695739902) Registrant - The Partners Co., Ltd. (695739902) Establishment Name Address ID/FEI Business Operations ENBIOSCIENCE CO., LTD. 695658751 manufacture(90034-010)