Label: MEDIKOII BIO CALMING RELIEF TONER- niacinamide, adenosine liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 72695-0012-1, 72695-0012-2 - Packager: THERANOTICS 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 May 29, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
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INACTIVE INGREDIENTS
Centella Asiatica Leaf Water, Butylene Glycol, Propanediol, Glycerin, 1,2-Hexanediol, Water, Pentylene Glycol, Resveratrol, Chlorogenic Acids, Ferulic Acid, Nicotinoyl Tripeptide-1, sh-Decapeptide-9, sh-Pentapeptide-5, Caffeoyl Tripeptide-1, sh-Oligopeptide-1, sh-Polypeptide-1, Centella Asiatica Callus Extract, Diospyros Kaki Leaf Extract, Morus Alba Bark Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Opuntia Coccinellifera Fruit Extract, Sodium Hyaluronate, Betaine, Citrus Aurantium Bergamia (Bergamot) Peel Oil, DisodiumEDTA, Lavandula Angustifolia (Lavender) Oil, Glyceryl Acrylate/Acrylic Acid Copolymer, Coceth-7, PEG-40 Hydrogenated Castor Oil,
PPG-1-PEG-9 Lauryl Glycol Ether, Panthenol, Propylene Glycol, Ethylhexylglycerin - PURPOSE
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WARNINGS
1.If you experience any symptoms such as redness, swelling, or itchiness during usage or from exposure to direct sunlight after usage, suspend use and consult a physician.
2. Do not use on wounds or other areas of skin irritation.
3. Storage and handling
a. Keep out of reach of children.
b. Keep away from direct sunlight. - KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- QUESTIONS
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MEDIKOII BIO CALMING RELIEF TONER
niacinamide, adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72695-0012 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 2 g in 100 mL ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.04 g in 100 mL Inactive Ingredients Ingredient Name Strength CENTELLA ASIATICA LEAF (UNII: 6810070TYD) Butylene Glycol (UNII: 3XUS85K0RA) Propanediol (UNII: 5965N8W85T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72695-0012-2 1 in 1 CARTON 05/01/2020 1 NDC:72695-0012-1 130 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 05/01/2020 Labeler - THERANOTICS CO.,LTD. (694963085) Registrant - THERANOTICS CO.,LTD. (694963085) Establishment Name Address ID/FEI Business Operations BIO-FD&C. Co., Ltd. 688203268 manufacture(72695-0012)
