Label: MUSTUS NONI AMPOULE- adenosine liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 73020-030-01, 73020-030-02 - Packager: Costory 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 9, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Inactive ingredients:
Morinda Citrifolia Extract, Propanediol, Glycerin, Methyl Gluceth-20, 1,2-Hexanediol, C12-14 Pareth-7, Trehalose, Water, Carbomer, Butylene Glycol, Tromethamine, Xanthan Gum, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Rutin, Dimethyl Sulfone, Ethylhexylglycerin, Salvia Officinalis (Sage) Oil, Macadamia Ternifolia Seed Oil, Vegetable Oil, Hydroxycinnamic Acid, dium EDTA, Coptis Chinensis Root Extract, Tocopherol
- PURPOSE
-
WARNINGS
Warnings:
For external use only. Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear. If any adverse reaction occurs, stop using the product and consult with the dermatologist if symptoms persist. Do not use on deep puncture wounds, animal bites or serious burns. Do not reuse the sheet once used. Keep out of reach of children. - KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
MUSTUS NONI AMPOULE
adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73020-030 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 Propanediol (UNII: 5965N8W85T) Glycerin (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73020-030-02 1 in 1 CARTON 03/01/2019 1 NDC:73020-030-01 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 03/01/2019 Labeler - Costory Co., Ltd (694893916) Registrant - Costory Co., Ltd (694893916) Establishment Name Address ID/FEI Business Operations COSON Co., Ltd._Osan Plant 689847210 manufacture(73020-030)
