Label: MIZON HYALURONIC ACID 100- adenosine liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 57718-290-01, 57718-290-02 - Packager: MIZON 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 July 24, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients:
Water,Methylpropanediol,1,2-Hexanediol,PEG-60 Hydrogenated Castor Oil,Sodium Hyaluronate,Glycerin,Triethylhexanoin,Diphenyl Dimethicone,Butylene Glycol,Ethylhexylglycerin,Carbomer,Tromethamine, Betula Alba Juice, ,Hydrogenated Lecithin, Polyglyceryl-10 Oleate,Portulaca Oleracea Extract,Alcohol,Disodium EDTA,Sclerotium Gum,Gentiana Lutea Root Extract,Achillea Millefolium Extract,Artemisia Absinthium Extract,Arnica Montana Flower Extract,Astragalus Membranaceus Root Extract,Copper Tripeptide -1,Scutellaria Baicalensis Root Extract,Propylene Glycol, Beta-Glucan,Vaccinium Macrocarpon (Cranberry) Fruit Extract,Rubus Idaeus (Raspberry) Fruit Extract,Prunus Serotina (Wild Cherry) Fruit Extract,Cornus Officinalis Fruit Extract,Punica Granatum Fruit Extract,Potassium Sorbate,Phenoxyethanol
- PURPOSE
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WARNINGS
Warnings:
1) In case of swelling, redness, itching or any severe allergic reactions while using the product,discontinue use and consult with a specialist. 2) Do not apply on injuries or wounded areas. 3) Precautions for storage and handling A) Keep out of reach of children. B) Store away from direct sunlight.
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MIZON HYALURONIC ACID 100
adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:57718-290 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.012 g in 30 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Methylpropanediol (UNII: N8F53B3R4R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:57718-290-02 1 in 1 CARTON 07/01/2018 1 NDC:57718-290-01 30 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 07/01/2018 Labeler - MIZON CO.,LTD. (694894201) Registrant - MIZON CO.,LTD. (694894201) Establishment Name Address ID/FEI Business Operations Coson Co., Ltd._Osan Plant 689847210 manufacture(57718-290)
