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LumaSilk Emulsion Level 02

Medically reviewed on Jun 12, 2017

Dosage form: emulsion
Ingredients: HYDROQUINONE 0.02g in 1g
Labeler: The Skin Atelier, Inc.
NDC Code: 71393-005

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.

Active Ingredient: 2% Hydroquinone

Directions: Wash face then apply to entire face morning and evening, avoiding the eye area.

Directions: Wash face then apply to entire face moring and evening, avoiding the eye area.

For external use only. When using this product avoid contact with eyes. If contact occurs, flush thoroughly with water. Keep out of reach of children. If swallowed get medical help or call Poison Control Center immediately.

Inactive Ingredients: Water, Alcohol SDA 40B, Squalane, Coenochloris Signiensis Extract (and) Maltodextrin (and) Lecithin, sodium Hyaluronate, Glycerin, dimethicone, Niacinimide, Ammonium Acryloyldimethyltaurate/Beheneth-25 Methacrylate Crosspolymer, Caprylhydroxamic Acid, Glyceryl Caprylate, Bidens Pilosa Extract, Elaeis Guineensis (Palm) Oil, Gossypium Herbaceum (Cotton) Seed Oil, Linum Usitatissimum (Linseed) Seed Oil, Sodium Stearoyl Lactylate, Cetyl Alcohol, Olus Oil/Vegetable Oil, Tocopheryl Acetate, Glycine Soja/Glycine Soja, (Soybean) Sterols, Sodium Carboxymethyl Betaglucan, Sodium Lactate, Carnosine, Phenyethylalcohol, sodium metabisulfite, disodium EDTA

Lightens skin. Restores skin luminosity. Instantly smoothes and softens skin.

Lightens skin. Restores skin luminosity. Instantly smoothes and softens skin.

Keep out of reach of children. If swallowed get medical help or call Poison Control Center immediately.

LUMASILK EMULSION LEVEL 02 
lumasilk emulsion level 02 emulsion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71393-005
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROQUINONE (HYDROQUINONE) HYDROQUINONE0.02 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
ELAEIS GUINEENSIS FRUIT BUTTER 
CORN OIL 
SODIUM CARBOXYMETHYL .BETA.-GLUCAN (DS 0.65-0.85) 
SODIUM LACTATE 
CARNOSINE 
GOSSYPIUM HERBACEUM WHOLE 
CETYL ALCOHOL 
DISODIUM HEDTA 
NIACINAMIDE 
LINUM USITATISSIMUM WHOLE 
GLYCERIN 
SODIUM STEAROYL LACTYLATE 
.ALPHA.-TOCOPHEROL ACETATE 
SOYBEAN OIL 
PHENYLETHYL ALCOHOL 
SODIUM METABISULFITE 
DIMETHICONE 200 
SQUALANE 
HYALURONATE SODIUM 
AMMONIUM ACRYLOYLDIMETHYLTAURATE/BEHENETH-25 METHACRYLATE CROSSPOLYMER (52000 MPA.S) 
GLYCERYL CAPRATE 
WATER 
ALCOHOL 
MALTODEXTRIN 
LECITHIN, SOYBEAN 
AMMONIUM ACRYLOYLDIMETHYLTAURATE 
CAPRYLHYDROXAMIC ACID 
BIDENS PILOSA LEAF 
COENOCHLORIS SIGNIENSIS 
Packaging
#Item CodePackage Description
1NDC:71393-005-3030 g in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other07/01/2017
Labeler - The Skin Atelier, Inc. (135049810)
Establishment
NameAddressID/FEIOperations
The Skin Atelier, Inc.135049810manufacture(71393-005)

 
The Skin Atelier, Inc.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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