Label: SMART RECOVERY FIRMING SERUM- adenosine liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 81211-040-01, 81211-040-02 - Packager: BIO-S CO.,LTD
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated December 15, 2020
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- Use
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Direction
- QUESTIONS
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INACTIVE INGREDIENTS
Water, Glycerin, Caprylic/Capric Triglyceride, Methylpropanediol, Hydrogenated Polyisobutene, Dipropylene Glycol, Glyceryl Stearate SE, Cetearyl Alcohol, Sorbitan Sesquioleate, 1,2-Hexanediol, Caprylyl Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Butylene Glycol, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Illicium Verum (Anise) Fruit Extract, Allantoin, Tromethamine, Sodium Hyaluronate, Xanthan Gum, Disodium EDTA, Anemarrhena Asphodeloides Root Extract, Ficus Carica (Fig) Fruit Extract, Morus Alba Fruit Extract, Punica Granatum Fruit Extract, Ginkgo Biloba Nut Extract, Caviar Extract, Chenopodium Quinoa Seed Extract, Helianthus Annuus (Sunflower) Seed Extract, Salvia Hispanica Seed Extract, Lens Esculenta (Lentil) Seed Extract, Linum Usitatissimum (Linseed) Seed Extract, Collagen Extract, Copper Tripeptide-1, Palmitoyl Pentapeptide-4, Tripeptide-1, Palmitoyl Tripeptide-1, Acetyl Hexapeptide-8, Hexapeptide-9, Nonapeptide-1
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SMART RECOVERY FIRMING SERUM
adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81211-040 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.02 g in 50 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) Methylpropanediol (UNII: N8F53B3R4R) HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ) Dipropylene Glycol (UNII: E107L85C40) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81211-040-02 1 in 1 CARTON 12/01/2020 1 NDC:81211-040-01 50 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 12/01/2020 Labeler - BIO-S CO.,LTD (690007651) Registrant - BIO-S CO.,LTD (690007651) Establishment Name Address ID/FEI Business Operations Interkos Co.,Ltd. 689850314 manufacture(81211-040)