OTC - ACTIVE INGREDIENT SECTION
Active Ingredient: 2% Hydroquinone
LumaSilk Emulsion Level 02
- Manufacturer
- The Skin Atelier, Inc.
- Effective date
- 2017-06-12
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-02 01:11:21
Label at a glance#
ProductLumaSilk Emulsion Level 02
Active ingredientHYDROQUINONE
Label structure9 sections
Label contents#
Full prescribing information#
INSTRUCTIONS FOR USE SECTION
Directions: Wash face then apply to entire face morning and evening, avoiding the eye area.
DOSAGE & ADMINISTRATION SECTION
Directions: Wash face then apply to entire face moring and evening, avoiding the eye area.
WARNINGS SECTION
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 INGREDIENT SECTION
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
INDICATIONS & USAGE SECTION
Lightens skin. Restores skin luminosity. Instantly smoothes and softens skin.
OTC - PURPOSE SECTION
Lightens skin. Restores skin luminosity. Instantly smoothes and softens skin.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If swallowed get medical help or call Poison Control Center immediately.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Products#
Every source-derived product name is available through these pages.
- LumaSilk Emulsion Level 02
- 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
- HYDROQUINONE
- 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
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 71393-005 | 71393-005-30 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 51c7d6d4-3652-0a53-e054-00144ff88e88 | 51c7d6d4-3651-0a53-e054-00144ff88e88 | 2017-06-12 | Warnings | 51c7d6d4-3652-0a53-e054-00144ff88e88 51c7d6d4-3651-0a53-e054-00144ff88e88 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.