CELLPIUM REAL MASK PACK- niacinamide patch

CELLPIUM REAL MASK PACK by

Drug Labeling and Warnings

CELLPIUM REAL MASK PACK by is a Otc medication manufactured, distributed, or labeled by MEDIPOST Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient: Niacinamide 2.00%

INACTIVE INGREDIENT

Inactive Ingredients: Water, Human Cord Blood Cell Conditioned Media, Glycereth-26, 1,2-Hexanediol, Diglycerin, Lactobacillus/Turmeric Ferment Filtrate, Bambusa Arundinacea Stem Extract, Portulaca Oleracea Extract, Bacillus/Soybean Ferment Extract, Centella Asiatica Extract, Biosaccharide Gum-1, Pentylene Glycol, Arginine, Carbomer, Sodium Hyaluronate, Adenosine, Disodium EDTA, Dipotassium Glycyrrhizate, Sodium Polyacrylate, Ascorbic Acid, Chondrus Crispus (Carrageenan), Glycerin, Palmitoyl Tripeptide-5

PURPOSE

Purpose: Skin Protectant

WARNINGS

Warnings: 1. If following symptoms occur, stop use and consult a doctor: red spots, swelling, itcihng, irritation, or symtoms on applied skin under direct sunlight. 2. Do not use on scarred skin, or if you have dermatitis or eczema 3. Keep the cap close on its product 4. Keep away from direct sunlight or heat. 5. Keep out of reach of children

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

INDICATIONS & USAGE

Indications & usage: Apply smoothly on the entire face in the morning and night.

DOSAGE & ADMINISTRATION

Dosage & administration: 2-3 times a week. Each mask is for one time use only.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CELLPIUM REAL MASK PACK 
niacinamide patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70506-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	Niacinamide	0.46 g  in 3

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Glycereth-26 (UNII: NNE56F2N14)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70506-020-01	3 in 1 CARTON; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		02/01/2016

Labeler - MEDIPOST Co.,Ltd. (688268817)

Registrant - MEDIPOST Co.,Ltd. (688268817)

Establishment
Name	Address	ID/FEI	Business Operations
MEDIPOST Co.,Ltd.		688268817	manufacture(70506-020)