LumaSilk Emulsion Level 03

Manufacturer
The Skin Atelier, Inc.
Effective date
2017-06-12
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:11:22

Label at a glance#

ProductLumaSilk Emulsion Level 03
Active ingredientHYDROQUINONE
Label structure7 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 morning and evening, avoiding the eye area.

WARNINGS SECTION

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.

WARNINGS AND PRECAUTIONS SECTION

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LumaSilk03.jpgLumaSilk03.jpg

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71393-00671393-006-30

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 30 matching rows.

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
51ca5b57-f48c-716d-e054-00144ff8d46c51ca5b57-f48b-716d-e054-00144ff8d46c2017-06-12WarningsExact identifier
spl id: 51ca5b57-f48c-716d-e054-00144ff8d46c
spl set id: 51ca5b57-f48b-716d-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.