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Lumasilk Emulsion

Generic name: hydroquinone
Dosage form: emulsion
Drug class: Topical depigmenting agents

Medically reviewed by Drugs.com. Last updated on May 24, 2021.

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.

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

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

Warning: 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 swalloed get medical help or call Poison Control Center immediately.

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.

Lumasilk Emulsion LEVEL 03
Lumasilk Emulsion level 03 emulsion
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:71393-006
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HYDROQUINONE (HYDROQUINONE) HYDROQUINONE 0.04 g in 1 g
Inactive Ingredients
Ingredient Name Strength
SODIUM METABISULFITE
DIMETHICONE 200
AMMONIUM ACRYLOYLDIMETHYLTAURATE/BEHENETH-25 METHACRYLATE CROSSPOLYMER (52000 MPA.S)
MALTODEXTRIN
CAPRYLHYDROXAMIC ACID
CORN OIL
BIDENS PILOSA LEAF
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
SQUALANE
HYALURONATE SODIUM
GLYCERYL CAPRATE
WATER
ALCOHOL
LECITHIN, SOYBEAN
AMMONIUM ACRYLOYLDIMETHYLTAURATE
ELAEIS GUINEENSIS FRUIT BUTTER
COENOCHLORIS SIGNIENSIS
Packaging
# Item Code Package Description
1 NDC:71393-006-30 30 g in 1 BOTTLE, PUMP
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 07/01/2017
Labeler - The Skin Atelier, Inc. (135049810)
Establishment
Name Address ID/FEI Operations
The Skin Atelier, Inc. 135049810 manufacture(71393-006)
The Skin Atelier, Inc.