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QUEENS ROSE ELYSEE CONCEN TRATE DUAL AMPOULE

Dosage form: liquid
Ingredients: Glycerin 0.19g in 8g
Labeler: Cdpharmtec Co.,ltd
NDC Code: 71252-090

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.

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

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

QUEENS ROSE ELYSEE CONCEN TRATE DUAL AMPOULE 
glycerin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71252-090
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Glycerin (GLYCERIN) Glycerin0.19 g  in 8 g
Inactive Ingredients
Ingredient NameStrength
Water 
Propanediol 
Packaging
#Item CodePackage Description
1NDC:71252-090-026 CONTAINER in 1 CARTON
1NDC:71252-090-018 g in 1 CONTAINER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other03/02/2017
Labeler - Cdpharmtec Co.,ltd (694209262)
Registrant - Cdpharmtec Co.,ltd (694209262)
Establishment
NameAddressID/FEIOperations
Cdpharmtec Co.,ltd694209262relabel(71252-090)
Establishment
NameAddressID/FEIOperations
Cosmax, Inc689049693manufacture(71252-090)

 
Cdpharmtec Co.,ltd

Medically reviewed on Mar 24, 2017

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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