Label: MIZON PEPTIDE 500- adenosine liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 57718-350-01, 57718-350-02 - Packager: MIZON CO.,LTD.
- Category: HUMAN OTC DRUG LABEL
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 26, 2018
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Inactive ingredients:
Water,Methylpropanediol,Butylene Glycol,Glycerin, Pentylene Glycol,PEG-60 Hydrogenated Castor Oil, 1,2-Hexanediol,Sodium Hyaluronate,Propanediol, Ethylhexylglycerin,Copper Tripeptide-1, Beta-Glucan,Disodium EDTA,Centella Asiatica Extract, Houttuynia Cordata Extract,Salvia Hispanica Seed Extract, Caprylyl Glycol,Acetyl Hexapeptide-8,Phenoxyethanol
- PURPOSE
-
WARNINGS
Warnings:
If you have any of the following problems with cosmetics, you should stop using it. If you continue to use it, your symptoms will worsen. Consult your dermatologist. 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 broken skin 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
-
INGREDIENTS AND APPEARANCE
MIZON PEPTIDE 500
adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:57718-350 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:57718-350-02 1 in 1 CARTON 07/01/2018 1 NDC:57718-350-01 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(57718-350)