Label: PIGE LL REAL SKIN EYE - sus scrofa skin patch 

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

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 01/13

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  • ACTIVE INGREDIENT

    pork skin
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  • INACTIVE INGREDIENT

    Water, Glycerin, Carrageenan, Ceratonia Siliqua Gum, Xanthan Gum, Butylene Glycol, Mineral Oil, Calcium Chloride, Etyl Alcohol, Lysine, Histidine, Arginine, Aspartic Acid, Threonine, Serine, Glutamic Acid, Proline, Glycine, Alanine, Valine, Methionine, Isoleucine, Leucine, Tyrosine, Phenylalanine, Cysteine, Hydrolyzed Collagen (0.1%), Coix Lacryma-Jobi Ma-yuen Seed Extract, Oryza Sativa (Rice) Bran Extract, Red Ginseng Extract, Argania Spinosa Kernel Oil, Adenosine, PEG-60 Hydrogenated Castor Oil, Disodium EDTA, Triethanolamine, Scutellaria Baicalensis Root Extract, Camellia Sinensis Leaf Extract, Houttuynia Cordata Extract, Artemisia Vulgaris Extract, Citrus Junos Fruit Extract, 1,2-Hexanediol, Caprylyl Glycol, Ethyl Hexanediol, Citrus Grandis (Grapefruit) Seed Extract, Bambusa Textilis Stem Extract, Pinus Palustris Leaf Extract, Propylparaben, Ethylparaben, Butylparaben, Isobutylparaben, Phenoxyethanol, Methylparaben, Chlorphenesin, Fragrance
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  • PURPOSE

    for the treatment of skin
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  • KEEP OUT OF REACH OF CHILDREN

    keep out or reach of the children
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  • INDICATIONS & USAGE

    attach biogel sheets around your eyes

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  • WARNINGS

    ■ Avoid using on blemishes, pimples, irritated or sunburned skin.
    ■ Avoid using on skin which is sensitive to bandages, tapes or peel-off masks.
    ■ Stop using if skin becomes reddish, swollen or itchy, during and after usage.
    ■ Avoid contact with eyes directly.


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  • DOSAGE & ADMINISTRATION

    for external use only
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  • INGREDIENTS AND APPEARANCE
    PIGE LL REAL SKIN EYE 
    sus scrofa skin patch
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:55282-3001
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SUS SCROFA SKIN (SUS SCROFA SKIN) SUS SCROFA SKIN 8 g  in 100 g
    Inactive Ingredients
    Ingredient Name Strength
    METHYLISOTHIAZOLINONE  
    WATER  
    GLYCERIN  
    CARRAGEENAN  
    CERATONIA SILIQUA WHOLE  
    XANTHAN GUM  
    BUTYLENE GLYCOL  
    MINERAL OIL  
    CALCIUM CHLORIDE  
    ALCOHOL  
    LYSINE  
    HISTIDINE  
    ARGININE  
    ASPARTIC ACID  
    THREONINE  
    SERINE  
    GLUTAMIC ACID  
    PROLINE  
    GLYCINE  
    ALANINE  
    VALINE  
    METHIONINE  
    ISOLEUCINE  
    LEUCINE  
    TYROSINE  
    PHENYLALANINE  
    CYSTEINE  
    COIX LACRYMA-JOBI SEED OIL  
    ORYZA SATIVA WHOLE  
    PANAX GINSENG ROOT OIL  
    ARGAN OIL  
    ADENOSINE  
    POLYOXYL 60 HYDROGENATED CASTOR OIL  
    EDETATE DISODIUM  
    TROLAMINE  
    SCUTELLARIA BAICALENSIS ROOT  
    TEA LEAF OIL  
    HOUTTUYNIA CORDATA FLOWERING TOP  
    ARTEMISIA VULGARIS ROOT  
    CITRUS JUNOS FRUIT  
    1,2-HEXANEDIOL  
    CAPRYLYL GLYCOL  
    ETHOHEXADIOL  
    CITRUS MAXIMA SEED  
    BAMBUSA TEXTILIS STEM  
    PINUS PALUSTRIS LEAF  
    PROPYLPARABEN  
    ETHYLPARABEN  
    BUTYLPARABEN  
    ISOBUTYLPARABEN  
    PHENOXYETHANOL  
    METHYLPARABEN  
    CHLORPHENESIN  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:55282-3001-1 9.6 g in 1 PACKAGE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 01/14/2013
    Labeler - Osung Co., Ltd (687407424)
    Registrant - Osung Co., Ltd (687407424)
    Establishment
    Name Address ID/FEI Business Operations
    JT Co., Ltd 557785196 manufacture(55282-3001)
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