Label: SMART RECOVERY HYDRATING TONER- adenosine liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 81211-010-01, 81211-010-02 - Packager: BIO-S CO.,LTD
- 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 December 10, 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, 1,2-Hexanediol, Butylene Glycol, Allantoin, Hydrolyzed Silk, Hydrogenated Polyisobutene, Sodium Hyaluronate, Chrysanthemum Morifolium Flower Extract, Sodium Hyaluronate Crosspolymer, Centella Asiatica Extract, Hydrolyzed Glycosaminoglycans, Polygonum Cuspidatum Root Extract, Scutellaria Baicalensis Root Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Camellia Sinensis Leaf Extract, Benzyl Glycol, Rosmarinus Officinalis (Rosemary) Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Hydrolyzed Hyaluronic Acid, Anemarrhena Asphodeloides Root Extract, Hyaluronic Acid, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Propanediol, Polyglyceryl-10 Laurate, Carbomer, Arginine, Xanthan Gum, Ethylhexylglycerin, Raspberry Ketone
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SMART RECOVERY HYDRATING TONER
adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81211-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.06 g in 150 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) 1,2-Hexanediol (UNII: TR046Y3K1G) Butylene Glycol (UNII: 3XUS85K0RA) Allantoin (UNII: 344S277G0Z) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81211-010-02 1 in 1 CARTON 12/01/2020 1 NDC:81211-010-01 150 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(81211-010)