Label: QUEENS ROSE ELYSEE CONCEN TRATE DUAL AMPOULE- glycerin liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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 March 24, 2017

If you are a consumer or patient please visit this version.

View All Sections
  • 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

    Image of carton

  • INGREDIENTS AND APPEARANCE
    QUEENS ROSE ELYSEE CONCEN TRATE DUAL AMPOULE 
    glycerin liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71252-090
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Glycerin (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) Glycerin0.19 g  in 8 g
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Propanediol (UNII: 5965N8W85T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71252-090-026 in 1 CARTON03/02/2017
    1NDC:71252-090-018 g in 1 CONTAINER; Type 0: Not a Combination Product
    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/FEIBusiness Operations
    Cdpharmtec Co.,ltd694209262relabel(71252-090)
    Establishment
    NameAddressID/FEIBusiness Operations
    Cosmax, Inc689049693manufacture(71252-090)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!