MEDISILKE  NIGHT- hydroquinone cream 
New GPC, Inc.

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.

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Medisilke
NIGHT CREAM

Active Ingredient

Hydroquinone 2%

Purpose

Skin bleaching agent.

Uses

For the gradual fading of brownish spots.

Inactive Ingredients

Water, SD Alcohol 40, Glyceryl Stearyl Citrate, Butylene Glycol, Ethylhexyl Palmitate, Methylpropanediol, Behenyl Alcohol, Glycerin,Sodium Hyaluronate, Disodium EDTA, Xanthan Gum, HydroxyethylCellulose, Cetearyl Alcohol, Cetearate-20, BHT, Glyceryl Dilaurate, Dimethicone, Hydroxyethyl Acrylate,Sodium AcryloylDimethyl Taurate Copolymer, Squalane, Polysorbate 60, Bambusa Vulgaris Leaf/Stem Extract, Pisum Sativum(Pea) Extract, Glucosamine HCl, Pyrus Malus (Apple) Fruit Extract, Glycine Soja (Soybean) Seed Extract, Retinol, Allyl Methacrylate Crosspolymer, Polysorbate 20, Camellia Sinensis Leaf Extract, EthylHexylglycerin, Methylisothiazolinone, Phenoxyethanol Capryl Glycol, Potassium Sorbate, Hexylene glycol, Glycyrrhiza Glabra (licorice) Root Extract. Citric Acid Tocopheryl Acetate, Caprylic/Capric Triglyceride, Macadamia Ternifola Seed Oil Retinyl Palmitate, Zea Mays (Corn Oil, Ubiquinone, Palmitic Acid, Thioctic Acid, Beta-Carotene, Heluanthus Annus (Sunflower) Seed Oil.

Directions

Adults: apply a small amount as a thin layer on the affected area twice daily to affected area or use as directed by a physician. If no improvement is seen after 3 months of treatment, use of this product should discontinued. Lightening effect of this product may not be noticeable when used on very dark skin.

Children under 12 years of age: do not use unless directed by a doctor.

Warnings

For external use only.

Avoid contact with eyes.

Some users of this product may experience a mild skin irritation.

If skin irritation becomes severe, stop use and consult a physician.

Do not use on children under 12 years age unless directed by a physician.

If swallowed get medical help or contact a posion control center.

Questions or Comments?

Moss Pharmaceuticals, P.O. Box 1426, Port Washington, NY 11060.
www.Medisilke.com

Manufactured by: NEW GPC INC., A1 Farm, EBD, Guyana under license for Moss Pharmaceuticals LLC, USA.

PRINCIPAL DISPLAY PANEL - 20g Tube Carton

Medisilke
NIGHT CREAM
Skin lightening cream / fades brown spots and skin discoloration

20g

PRINCIPAL DISPLAY PANEL - 20g Tube Carton
MEDISILKE   NIGHT
hydroquinone cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65588-2230
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE) HYDROQUINONE2 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
ETHYLHEXYL PALMITATE (UNII: 2865993309)  
METHYLPROPANEDIOL (UNII: N8F53B3R4R)  
DOCOSANOL (UNII: 9G1OE216XY)  
GLYCERIN (UNII: PDC6A3C0OX)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
XANTHAN GUM (UNII: TTV12P4NEE)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
SQUALANE (UNII: GW89575KF9)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
BAMBUSA VULGARIS LEAF (UNII: EMY54R518C)  
BAMBUSA VULGARIS STEM (UNII: SMR633LHTC)  
APPLE (UNII: B423VGH5S9)  
SOYBEAN (UNII: L7HT8F1ZOD)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
RETINOL (UNII: G2SH0XKK91)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
MACADAMIA OIL (UNII: 515610SU8C)  
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
CORN OIL (UNII: 8470G57WFM)  
UBIDECARENONE (UNII: EJ27X76M46)  
PALMITIC ACID (UNII: 2V16EO95H1)  
ALPHA LIPOIC ACID (UNII: 73Y7P0K73Y)  
BETA CAROTENE (UNII: 01YAE03M7J)  
HELIANTHUS ANNUUS (UNII: BKJ0J3D1BP)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65588-2230-31 in 1 CARTON
120 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart358A12/01/2009
Labeler - New GPC, Inc. (895025443)
Establishment
NameAddressID/FEIBusiness Operations
New GPC, Inc.895025443MANUFACTURE

Revised: 10/2010
Document Id: b04435ae-1f67-4bc6-ad07-eceb51ea3d37
Set id: 2e53471e-ad03-4d6b-9384-4af374bb5f74
Version: 1
Effective Time: 20101013
 
New GPC, Inc.