Label: ELDEEN AGE TWENTY ONE MIFITPATCH AND SERUM- sodium hyaluronate kit

  • NDC Code(s): 71184-1000-1, 71184-2000-1, 71184-3000-1
  • Packager: Small Lab Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL

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 June 2, 2019

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • ACTIVE INGREDIENT

    SODIUM HYALURONATE

  • INACTIVE INGREDIENT

    SERUM: WATER, ALGIN, GLYCERIN, BETAINE, ETC.

    PATCH: WATER, CELLULOSE GUM, GLYCERIN, TREHALOSE, ETC.

  • PURPOSE

    Skin Care

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of the children

  • INDICATIONS & USAGE

    1. After cleansing, keep your skin clearly.

    2. Apply serum on your face and massage with your finger lightly.

    3. Carefully remove both films. (white and transparence)

    4. Stick the patch to target areas of concern (under eyes, smile, and frown lines) and gently press down on the patch for 2-3 minutes.

    5. Leave in place for 2 hours or more.

  • WARNINGS

    1. Do not use in the following cases(Eczema and scalp wounds)
    2.Side Effects
    1)Due to the use of this druf if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your phamacisr or doctor
    3.General Precautions
    1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately
    2)This product is for exeternal use only. Do not use for internal use
    4.Storage and handling precautions
    1)If possible, avoid direct sunlight and store in cool and area of low humidity
    2)In order to maintain the quality of the product and avoid misuse
    3)Avoid placing the product near fire and store out in reach of children

  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    ELDEEN AGE TWENTY ONE MIFITPATCH AND SERUM 
    sodium hyaluronate kit
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71184-3000
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71184-3000-11 in 1 PACKAGE; Type 0: Not a Combination Product10/01/2018
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 11 POUCH 1 g
    Part 24 POUCH 80 mg
    Part 1 of 2
    ELDEEN AGE TWENTY ONE SERUM 
    sodium hyaluronate liquid
    Product Information
    Item Code (Source)NDC:71184-1000
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONATE SODIUM0.4298 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71184-1000-11 g in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other11/08/201806/03/2019
    Part 2 of 2
    ELDEEN AGE TWENTY ONE MIFITPATCH 
    sodium hyaluronate patch
    Product Information
    Item Code (Source)NDC:71184-2000
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONATE SODIUM6.14 g  in 100 mg
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71184-2000-120 mg in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/01/201806/03/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/01/2018
    Labeler - Small Lab Co., Ltd. (688438425)
    Registrant - Small Lab Co., Ltd. (688438425)
    Establishment
    NameAddressID/FEIBusiness Operations
    Small Lab Co., Ltd.688438425manufacture(71184-1000, 71184-2000, 71184-3000) , label(71184-1000, 71184-2000, 71184-3000) , pack(71184-1000, 71184-2000, 71184-3000)