Label: ALL IN ONE DUAL MASK- glycerin patch

  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated March 29, 2016

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  • ACTIVE INGREDIENT

    Faceline Power Patch Active Ingredient: Glycerin 25.0%

  • INACTIVE INGREDIENT

    Multi Intensive Mask Inactive Ingredients: Water, Butylene Glycol, Glycereth-26, Betaine, Propylene Glycol, Niacinamide, Bis-PEG-18 Methyl Ether Dimethyl Silane, Phenoxyethanol, Chlorphenesin, PEG-40 Hydrogenated Castor Oil, PPG-26-Buteth-26, Carbomer, Triethanolamine, Bacillus/Soybean Ferment Extract, Panax Ginseng Root Extract, Palmitoyl Oligopeptide, Palmitoyl Tetrapeptide-7, Adenosine, Disodium EDTA, Dipotassium Glycyrrhizate, Allantoin, Chondrus Crispus (Carrageenan), Torreya Nucifera Extract, Cornus Kousa Extract, Rosa Multiflora Fruit Extract, Chloranthus Glaber Extract, Musa Basjoo Extract, Ethyl Ascorbyl Ether, Panax Ginseng Callus Culture Extract, Tocopheryl Acetate, Fragrance, Magnolia Officinalis Bark Extract, rh-Oligopeptide-1, Glycerin, Chrysanthellum Indicum Extract, Rheum Palmatum Root/Stalk Extract, Asarum Sieboldi Root Extract, Larix Sibirica Wood Extract, Quercus Mongolia Leaf Extract, Persicaria Hydropiper Extract, Illicium Verum (Anise) Fruit Extract, Corydalis Turtschaninovii Root Extract, Coptis Japonica Root Extract, Machilus Thunbergii Bark Extract, Sodium Hyaluronate, Argania Spinosa Kernel Oil, Palmitoyl Tripeptide-5

    Faceline Power Patch Inactive Ingredients: Water, Sodium Polyacrylate, 1,2-Hexanediol, Carbomer, Aluminum Glycinate, Tartaric Acid, Titanium Dioxide, Hydrolyzed Collagen, Sodium Hyaluronate, Phosphatidylcholine, Adenosine, Ascorbic Acid, Silk Amino Acids

  • PURPOSE

    Purpose: Skin Protectant

  • WARNINGS

    Warnings: 1. If the following symptoms arise upon use of the cosmetic product, immediately discontinue use and consult a dermatologist, for continued use may aggravate the symptoms. A. Redness, swelling, itchiness, stimulation, or other symptoms B. Occurrence of the above symptoms upon exposure to direct sunlight. 2. Do not use on areas with wounds, eczema, or dermatitis. 3. Caution for storing. A. Put the lid back after using it. B. Keep it out of infants or children’s reach C. Don’t Keep it in the place where the temperature is extremely hot or cold and exposed to the direct sunlight D. Avoid using around the eye area.

  • KEEP OUT OF REACH OF CHILDREN

    Keep it out of infants or children’s reach

  • INDICATIONS & USAGE

    Indications & Usage: 1. After washing, prepare for mask treatment and tone skin by moisturizing your skin 2. Wear the mask sheet (upper), follow the cutting leave the eyes a space - How to put ear-hold patch- Place the sheet cutting line down. (It can be torn if you pull too much) 3. Take out the mask sheet from the package and remove protecting film. Hold the edges of sheet flat-side up. Pull the sheet gently to both sides along your face line and hook around your ears. 4. Leave the mask 10 to 20 minutes and take it off. 5. Massage and dab the face gently let the essence absorb into skin cell well.

  • DOSAGE & ADMINISTRATION

    Dosage & Administration: Use immediately after opening. 2-3 times a week.

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    ALL IN ONE DUAL MASK 
    glycerin patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70566-040
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Glycerin (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) Glycerin3 g  in 10 
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70566-040-0110 in 1 CARTON; Type 1: Convenience Kit of Co-Package
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34702/01/2016
    Labeler - MODECOS CO., LTD. (689605567)
    Registrant - MODECOS CO., LTD. (689605567)
    Establishment
    NameAddressID/FEIBusiness Operations
    MODECOS CO., LTD.689605567manufacture(70566-040)