Label: ELCURE Q SERUM - adenosine 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 July 13, 2013

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

  • ACTIVE INGREDIENT

    adenosin


    Close
  • INACTIVE INGREDIENT

    arbutin, niacinamide, scutellaria baicalensis root extract, paeonia suffruticosa root extract, water, thickening agent, fragrance


    Close
  • PURPOSE

    cosmetics wit double action of skin wrinkle reduction and skin whitening


    Close
  • KEEP OUT OF REACH OF CHILDREN

    keep out or reach of the children


    Close
  • INDICATIONS & USAGE

    - apply sufficient quantity to intended part

    - absorb it into skin softly with doing massage every morning and night after cleansingk

    Close
  • WARNINGS

    store at room temperature
    avoid exposing the product direct to sunlight, high temperature and humidity



    Close
  • DOSAGE & ADMINISTRATION

    for external use only


    Close
  • INGREDIENTS AND APPEARANCE
    ELCURE Q SERUM 
    adenosine liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:75949-6001
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 25 mg  in 50 mL
    Inactive Ingredients
    Ingredient Name Strength
    ARBUTIN (UNII: C5INA23HXF)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    PAEONIA SUFFRUTICOSA ROOT (UNII: 7M7E9A2C8J)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:75949-6001-1 50 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 07/18/2013
    Labeler - Elcure Co., Ltd. (557800490)
    Registrant - Elcure Co., Ltd. (557800490)
    Establishment
    Name Address ID/FEI Business Operations
    Elcure Co., Ltd. 557800490 manufacture(75949-6001)
    Close