QUEENS ROSE ELYSEE CONCEN TRATE DUAL AMPOULE- glycerin liquid
Cdpharmtec Co.,ltd

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.

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ACTIVE INGREDIENT

Active ingredients: Glycerin 2.46%

INACTIVE INGREDIENT

Inactive ingredients: Water, Propanediol, Betaine, Glycerin, Alcohol Denat.,Pentylene Glycol, Squalane, Butylene Glycol,1,2-Hexanediol, Ceramide NP, Human Stem Cell Conditioned Media, PEG-60 Hydrogenated Castor Oil, Phenoxyethanol, Pyrus Malus (Apple) Fruit Water, Phospholipids, Phytosphingosine, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Tromethamine, Caprylyl Glycol, Sodium Hyaluronate, Fragrance(Parfum), Disodium EDTA, Xanthan Gum, Phytosterols, Rosa Damascena Flower Water, Tropolone, Acid Red 18 (CI 16255), Nelumbo Nucifera Flower Extract, Prunus Mume Fruit Extract,Polyglutamic Acid

PURPOSE

Purpose: Skin Moisturizing

WARNINGS

Warnings: For external use only When using this product do not get into eyes, Stop use and ask a doctor if rash occurs. Do not use on - deep puncture wounds - animal bites - serious burns.

KEEP OUT OF REACH OF CHILDREN

INDICATIONS & USAGE

Indications & Usage: Helps prevent and relieve chapped or cracked skin.

DOSAGE & ADMINISTRATION

Dosage & Administration: - Take a proper amount of product, and spread it evenly over the entire face. - Apply in daily skin care routine.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

QUEENS ROSE ELYSEE CONCEN TRATE DUAL AMPOULE
glycerin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:71252-090
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Glycerin (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	Glycerin	0.19 g in 8 g

Ingredient Name	Strength
Inactive Ingredients
Water (UNII: 059QF0KO0R)
Propanediol (UNII: 5965N8W85T)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:71252-090-02	6 in 1 CARTON	03/02/2017
1	NDC:71252-090-01	8 g in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		03/02/2017

Labeler - Cdpharmtec Co.,ltd (694209262)

Registrant - Cdpharmtec Co.,ltd (694209262)

Name	Address	ID/FEI	Business Operations
Establishment
Cdpharmtec Co.,ltd		694209262	relabel(71252-090)

Name	Address	ID/FEI	Business Operations
Establishment
Cosmax, Inc		689049693	manufacture(71252-090)