Label: WELLAGE FAMILY MASK LARGE- sodium hyaluronate patch

  • 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 September 12, 2016

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  • ACTIVE INGREDIENT

    Sodium Hyaluronate

  • INACTIVE INGREDIENT

    Water, Dipropylene Glycol, Glycereth-26, Erythritol, Diethoxyethyl Succinate, Chamaecyparis Obtusa Water, Panthenol, Polyglyceryl-10 Laurate, Carbomer, Arginine, 1,2-Hexanediol, Allantoin, Chamaecyparis Obtusa Oil, Pantolactone, Disodium EDTA

  • PURPOSE

    Skin protectant

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    1. Remove mask from pouch and place on face for 15-20 minutes.
    2. Pat in remaining essence to absorb into skin.
      *Masks should be stored lying flat to ensure essence is evenly distributed throughout the sheets.
  • WARNINGS

    1. Do not use in the following cases(Eczema and scalp wounds)

    2.Side Effects

    1)Due to the use of this product, if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your pharmacist 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

    l

  • INGREDIENTS AND APPEARANCE
    WELLAGE FAMILY MASK LARGE 
    sodium hyaluronate patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69346-0008
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONATE SODIUM0.056 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ERYTHRITOL (UNII: RA96B954X6)  
    ALLANTOIN (UNII: 344S277G0Z)  
    CHAMAECYPARIS OBTUSA WOOD OIL (UNII: P2OMP71Y62)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69346-0008-110 in 1 PACKAGE09/08/2016
    125 mL in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/01/2016
    Labeler - HUGEL PHARMA CO.,LTD (688400184)
    Registrant - HUGEL PHARMA CO.,LTD (688400184)
    Establishment
    NameAddressID/FEIBusiness Operations
    HUGEL PHARMA CO.,LTD688400184manufacture(69346-0008)