PIGE LL REAL SKIN NECK PACK- sus scrofa skin liquid

PiGe ll Real Skin Neck Pack by

Drug Labeling and Warnings

PiGe ll Real Skin Neck Pack by is a Otc medication manufactured, distributed, or labeled by Osung Co., Ltd, JT Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

pork skin

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

PURPOSE

for the treatment of skin

KEEP OUT OF REACH OF CHILDREN

keep out or reach of the children

INDICATIONS & USAGE

attach biogel sheets to fit your neck

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.

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PIGE LL REAL SKIN NECK PACK 
sus scrofa skin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55282-2001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SUS SCROFA SKIN (UNII: 3EM4VW6TQN) (SUS SCROFA SKIN - UNII:3EM4VW6TQN)	SUS SCROFA SKIN	8 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CARRAGEENAN (UNII: 5C69YCD2YJ)
CERATONIA SILIQUA WHOLE (UNII: 12640NNX2M)
XANTHAN GUM (UNII: TTV12P4NEE)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
MINERAL OIL (UNII: T5L8T28FGP)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
ALCOHOL (UNII: 3K9958V90M)
LYSINE (UNII: K3Z4F929H6)
HISTIDINE (UNII: 4QD397987E)
ARGININE (UNII: 94ZLA3W45F)
ASPARTIC ACID (UNII: 30KYC7MIAI)
THREONINE (UNII: 2ZD004190S)
SERINE (UNII: 452VLY9402)
GLUTAMIC ACID (UNII: 3KX376GY7L)
PROLINE (UNII: 9DLQ4CIU6V)
GLYCINE (UNII: TE7660XO1C)
ALANINE (UNII: OF5P57N2ZX)
VALINE (UNII: HG18B9YRS7)
METHIONINE (UNII: AE28F7PNPL)
ISOLEUCINE (UNII: 04Y7590D77)
LEUCINE (UNII: GMW67QNF9C)
TYROSINE (UNII: 42HK56048U)
PHENYLALANINE (UNII: 47E5O17Y3R)
CYSTEINE (UNII: K848JZ4886)
COIX LACRYMA-JOBI SEED OIL (UNII: 271N0Q057Z)
ORYZA SATIVA WHOLE (UNII: 84IVV0906Z)
PANAX GINSENG ROOT OIL (UNII: P9T4K47OM0)
ARGAN OIL (UNII: 4V59G5UW9X)
ADENOSINE (UNII: K72T3FS567)
POLYOXYL 60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)
EDETATE DISODIUM (UNII: 7FLD91C86K)
TROLAMINE (UNII: 9O3K93S3TK)
SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
TEA LEAF OIL (UNII: VC855RRT77)
HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)
ARTEMISIA VULGARIS ROOT (UNII: 32MP823R8S)
CITRUS JUNOS FRUIT (UNII: 53KHW58C1V)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ETHOHEXADIOL (UNII: M9JGK7U88V)
CITRUS MAXIMA SEED (UNII: 083X55C543)
BAMBUSA TEXTILIS STEM (UNII: 7L05M929Y1)
PINUS PALUSTRIS LEAF (UNII: OT6R5143A1)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
ETHYLPARABEN (UNII: 14255EXE39)
BUTYLPARABEN (UNII: 3QPI1U3FV8)
ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
METHYLPARABEN (UNII: A2I8C7HI9T)
CHLORPHENESIN (UNII: I670DAL4SZ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55282-2001-1	32 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(55282-2001)