ICELAND BRIGHTENING WATERY CREA M

Manufacturer
NATURE REPUBLIC CO., LTD. | Kolmar Korea Co., Ltd.
Effective date
2017-07-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:15:06

Label at a glance#

ProductICELAND BRIGHTENING WATERY CREA M
Active ingredientDIMETHICONE
Label structure8 sections

Indications and uses

Uses: The brightening watery cream brightens and moisturizes skin with ingredients such as glacial water from the perennial snow of pristine Iceland and sand lily (Pancratium Maritimum Extract) that blossoms from sand with its strong life energy.

Dosage and administration

Directions: At the last step of skin care, apply an appropriate amount on the entire face and gently pat to promote absorption into skin.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: DIMETHICONE 5.99%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients: Water, Cyclopentasiloxane, Glycerin, Methylpropanediol, Hydrogenated Poly(C6-14 Olefin), Water, 1,2-Hexanediol,Isodecyl Neopentanoate, Niacinamide, Dimethicone/Vinyl Dimethicone Crosspolymer, Ammonium Acryloyldimethyltaurate/Vp Copolymer, Betaine, Biosaccharide Gum-1, Bifida Ferment Lysate, Polyquaternium-51, Beta-Glucan, Dimethiconol, Squalane, Dipropylene Glycol, Fragrance, Algae Extract, Butylene Glycol, Eclipta Prostrata Leaf Extract, Hydrogenated Polyisobutene, Centella Asiatica Extract, Ficus Carica (Fig) Fruit Extract, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Alcohol, Amaranthus Caudatus Seed Extract, Ulmus Davidiana Root Extract, Olea Europaea (Olive) Leaf Extract, Pancratium Maritimum Extract, Polysorbate 60, Hydrogenated Lecithin, Argania Spinosa Kernel Oil, Isononyl Isononanoate, Polyglyceryl-10 Stearate, Butyrospermum Parkii (Shea) Butter, Cetearyl Alcohol, Fructooligosaccharides, Polyglyceryl-2 Dipolyhydroxystearate, Stearic Acid, Sodium Hyaluronate, Lecithin,Hydrolyzed Hyaluronic Acid, Inulin Lauryl Carbamate, Ascorbyl Glucoside, Zinc Pca, Disodium Stearoyl Glutamate, Glutathione, Ceramide Np, Acetic Acid, Maltodextrin, Saccharide Hydrolysate, Lactic Acid, Potassium Sorbate

PURPOSE

OTC - PURPOSE SECTION

Purpose: Skin Protectant

WARNINGS

WARNINGS SECTION

Warnings: For external use only Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear. Keep Out of Reach of Children

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

Uses

INDICATIONS & USAGE SECTION

Uses: The brightening watery cream brightens and moisturizes skin with ingredients such as glacial water from the perennial snow of pristine Iceland and sand lily (Pancratium Maritimum Extract) that blossoms from sand with its strong life energy.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions: At the last step of skin care, apply an appropriate amount on the entire face and gently pat to promote absorption into skin.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of catonImage of caton

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51346-48651346-486-01, 51346-486-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIMETHICONE92RU3N3Y1OACTIB
Water059QF0KO0RIACT
GlycerinPDC6A3C0OXIACT

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
b99e1ec4-53c8-44e9-8236-2000ab5e72bb9e35d8c8-a4eb-4778-bb87-8f0208a8ffe82020-01-14WarningsExact identifier
spl set id: 9e35d8c8-a4eb-4778-bb87-8f0208a8ffe8

Reported adverse events (FAERS/openFDA)#

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