DE MEDICOTEM ILLUMINATING WHITE CELL AMPOULE- niacinamide liquid

De medicotem illuminating white cell ampoule by

Drug Labeling and Warnings

De medicotem illuminating white cell ampoule by is a Otc medication manufactured, distributed, or labeled by BELLANEZ, Nature Intro Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients: Niacinamide 2.2%

INACTIVE INGREDIENT

Inactive ingredients:
Water, Dipropylene Glycol, Glycereth-26, Human Stem Cell Conditioned Media, Glycerin, Butylene Glycol, 1,2-HEXANEDIOL, C12-13 Pareth-9, Synthetic Fluorphlogopite, Titanium Dioxide(CI77891), TinOxide, Camellia sinensis Callus Culture extracts, Bambusa Vulgaris Callus Culture Extract, Hydroxyethylacrylate/ Sodium Acryloyldimethyltaurate Copolymer, Butyrospermum Parkii(Shea Butter), Xanthan Gum, Betaine, Ferulic Acid, Pentylene Glycol, Beta-Glucan, Sclerotium gum, Fullerenes, Astaxanthin, Polyglyceryl-10 DIIsostearate, Caprylic/Capric Triglyceride, Sodium Hyaluronate, Hydrogenated Lecithin, Pvp

PURPOSE

Purpose: Skin Brightening

WARNINGS

Warnings:
For external use only
Avoid contact with eyes.
Discontinue use if signs of irritation or rashes appear.
Do not use on the wounded areas.
Keep out of reach of children.
Keep away from direct sunlight

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

Uses

Uses:
■ Shines skin softly.
■ Corrects skin tone.
■ Protects the skin barrier and skin cell
■ Helps skin recovery
■ Calms down the worn-out skin
■ Maintain clear and bright skin

Directions

Directions:
■ Every morning and night, after using a toner, apply it in a bottle(5ml) evenly over the skin three to four times and make it absorb. Recommended for use within two weeks of release.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DE MEDICOTEM ILLUMINATING WHITE CELL AMPOULE 
niacinamide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72799-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	0.11 g  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Dipropylene Glycol (UNII: E107L85C40)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72799-010-02	10 in 1 CARTON	12/01/2018
1	NDC: 72799-010-01	5 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		12/01/2018

Labeler - BELLANEZ (694798857)

Registrant - BELLANEZ (694798857)

Establishment
Name	Address	ID/FEI	Business Operations
Nature Intro Co., Ltd.		688282814	manufacture(72799-010)