FIRST C SUPERFULL- arbutin, adenosine cream 
LIZK Co., Ltd.

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.

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69725-002 Deactivation

Arbutin 2%

Adenosine 0.04%

Skin Protectant

Helps to improve skin brightness

Apply proper amount and gently massage on face with fingertips until absorbed

For external use only
Do not use on damaged or broken skin
Stop using and ask a doctor if rash occurs
When using this product, keep out of eyes. Rinse with water to remove

Keep out of reach of the children. If product is swallowed, get medical help or contact a poison control center right away.

Water, Glycerin, Butylene Glycol, Cetyl Ethylhexanoate, Hydrogenated Poly(C6-14 Olefin), Betaine, Mineral Oil, Butylene Glycol Dicaprylate/Dicaprate, Diisostearyl Malate, Microcrystalline Wax, Glyceryl Stearate, Polysorbate 60, Capsicum Annuum Fruit Extract, Superoxide Dismutase, sh-Oligopeptide-1, sh-Oligopeptide-2, sh-Polypeptide-1, sh-Polypeptide-10, Xanthophylls, Glutathione, Cudrania Tricuspidata Bark Extract, Viscum Album (Mistletoe) Extract, Phaseolus Radiatus Seed Extract, Ganoderma Lucidum (Mushroom) Extract, Tremella Fuciformis (Mushroom) Extract, Boerhavia Diffusa Root Extract, Levan, Allantoin, Panthenol, Caffeine, Sodium Hyaluronate, Tocopherol, Tocopheryl Acetate, Dimethicone, Cyclopentasiloxane, Stearic Acid, Cyclohexasiloxane, Beeswax, PEG-100 Stearate, Cetearyl Alcohol, Sorbitan Stearate, Phenoxyethanol, Sodium Acrylate/Sodium Acryloyldimethyl, Taurate Copolymer, Ethyl Hexanediol, Pentylene Glycol, 1,2-Hexanediol, Chlorphenesin, Caprylyl Glycol, Trideceth-6, Lecithin, Sodium Phosphate, Fragrance

image description

FIRST C SUPERFULL 
arbutin, adenosine cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69725-002
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ARBUTIN (UNII: C5INA23HXF) (ARBUTIN - UNII:C5INA23HXF) ARBUTIN1 mg  in 50 mL
ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE0.2 mg  in 50 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
CETYL ETHYLHEXANOATE (UNII: 134647WMX4)  
HYDROGENATED POLY(C6-14 OLEFIN; 2 CST) (UNII: P0TX083987)  
BETAINE (UNII: 3SCV180C9W)  
MINERAL OIL (UNII: T5L8T28FGP)  
BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: 75D21FL1PI)  
DIISOSTEARYL MALATE (UNII: QBS8A3XZGQ)  
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
PAPRIKA (UNII: X72Z47861V)  
SUPEROXIDE DISMUTASE (SACCHAROMYCES CEREVISIAE) (UNII: W2T4YRA9AD)  
NEPIDERMIN (UNII: TZK30RF92W)  
MECASERMIN (UNII: 7GR9I2683O)  
BASIC FIBROBLAST GROWTH FACTOR (HUMAN) (UNII: S3529G9M9V)  
LUTEIN (UNII: X72A60C9MT)  
GLUTATHIONE (UNII: GAN16C9B8O)  
MACLURA TRICUSPIDATA BARK (UNII: XU4SO65V1I)  
VISCUM ALBUM WHOLE (UNII: E6839Q6DO1)  
MUNG BEAN (UNII: 1LIB31N73G)  
REISHI (UNII: TKD8LH0X2Z)  
TREMELLA FUCIFORMIS WHOLE (UNII: 4938BNS0GU)  
BOERHAVIA DIFFUSA ROOT (UNII: KR0SR09KYL)  
ALLANTOIN (UNII: 344S277G0Z)  
PANTHENOL (UNII: WV9CM0O67Z)  
CAFFEINE (UNII: 3G6A5W338E)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
TOCOPHEROL (UNII: R0ZB2556P8)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
YELLOW WAX (UNII: 2ZA36H0S2V)  
PEG-100 STEARATE (UNII: YD01N1999R)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)  
ETHOHEXADIOL (UNII: M9JGK7U88V)  
PENTYLENE GLYCOL (UNII: 50C1307PZG)  
1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
TRIDECETH-6 (UNII: 3T5PCR2H0C)  
EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)  
SODIUM PHOSPHATE (UNII: SE337SVY37)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69725-002-021 in 1 CARTON03/05/201812/17/2018
1NDC:69725-002-0150 mL in 1 CONTAINER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other03/05/201812/17/2018
Labeler - LIZK Co., Ltd. (688442249)
Registrant - LIZK Co., Ltd. (688442249)
Establishment
NameAddressID/FEIBusiness Operations
VITA Nature Co., Ltd694816771manufacture(69725-002)

Revised: 12/2018
Document Id: 7d41068f-12f8-6a0d-e053-2a91aa0a417f
Set id: 6e421fe3-18e0-47f7-9fa2-dcbef6d86a0f
Version: 3
Effective Time: 20181217
 
LIZK Co., Ltd.