Cellpium preamiumEX hybrid eye contour

Manufacturer
MEDIPOST Co.,Ltd. | Kolmar Korea Co., Ltd.
Effective date
2016-03-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:27:56

Label at a glance#

ProductCellpium preamiumEX hybrid eye contour
Active ingredientDIMETHICONE
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: DIMETHICONE 2.58%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: WATER, CYCLOPENTASILOXANE, GLYCERIN, 1,2-HEXANEDIOL, HYDROGENATED POLY(C6-14 OLEFIN), NIACINAMIDE, CETYL ALCOHOL, GLYCERYL STEARATE, DIOSCOREA JAPONICA ROOT EXTRACT, PEG-100 STEARATE, BUTYROSPERMUM PARKII (SHEA) BUTTER, BETAINE, CORN STARCH MODIFIED, METHYLPROPANEDIOL, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, PIPER METHYSTICUM LEAF/ROOT/STEM EXTRACT, C12-14 PARETH-7, ARCTIUM LAPPA ROOT EXTRACT, HUMAN CORD BLOOD CELL CONDITIO NED MEDIA, PENTAERYTHRITYL DISTEARATE, PHELLINUS LINTEUS EXTRACT, TRIDECETH-6, SOLUBLE COLLAGEN, HYDROGENATED LECITHIN, C12-13 PARETH-23, DIVINYLDIMETHICONE/DIMETHICONE COPOLYMER, PHELLODENDRON AMURENSE BARK EXTRACT, TOCOPHERYL ACETATE, PORTULACA OLERACEA EXTRACT, PUERARIA THUNBERGIANA ROOT EXTRACT, CNIDIUM OFFICINALE ROOT EXTRACT, GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT, PAEONIA LACTIFLORA ROOT EXTRACT, PEG-75 STEARATE, C12-13 PARETH-3, POLYQUATERNIUM-51, LAVANDULA ANGUSTIFOLIA (LAVENDER) FLOWER/LEAF/STEM EXTRACT, ROSMARINUS OFFICINALIS (ROSEMARY) EXTRACT, NELUMBO NUCIFERA CALLUS CULTURE EXTRACT, GLYCOSYL TREHALOSE, HYDROGENATED POLYISOBUTENE, SQUALANE, ALOE BARBADENSIS LEAF JUICE, CETETH-20, STEARETH-20, ALCOHOL, CAPRYLIC/CAPRIC TRIGLYCERIDE, FRAGRANCE, HYDROGENATED STARCH HYDROLYSATE, ARGANIA SPINOSA KERNEL OIL, RAFFINOSE, ADENOSINE, BIOSACCHARIDE GUM-1, SODIUM HYALURONATE, ISONONYL ISONONANOATE, POLYGLYCERYL-10 STEARATE, BISABOLOL, CETEARYL ALCOHOL, LECITHIN, POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE, STEARIC ACID, BUTYLENE GLYCOL, POLYSORBATE 60, PEG/PPG-18/18 DIMETHICONE, SODIUM POLYACRYLATE, CERAMIDE NP, PENTYLENE GLYCOL, PANTHENOL, CHOLESTEROL, XANTHAN GUM, CARAMEL, DICAPRYLYL CARBONATE, INULIN LAURYL CARBAMATE, PROPYLENE GLYCOL, SUCROSE DISTEARATE, FOLIC ACID, ACACIA SENEGAL GUM, DISODIUM STEAROYL GLUTAMATE, TROMETHAMINE, ACETYL GLUCOSAMINE, HYALURONIC ACID, HYDROLYZED COLLAGEN, ETHYLHEXYLGLYCERIN, ASCORBIC ACID, GENISTEIN METHYL ETHER, PALMITOYL PENTAPEPTIDE-4, PHENOXYETHANOL

PURPOSE

OTC - PURPOSE SECTION

Purpose: Skin Protectant

WARNINGS

WARNINGS SECTION

Warnings: 1. If following symptoms occur, stop use and consult a doctor: red spots, swelling, itcihng, irritation, or symtoms on applied skin under direct sunlight. 2. Do not use on scarred skin, or if you have dermatitis or eczema 3. Keep the cap close on its product 4. Keep away from direct sunlight or heat. 5. 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

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

Indications & usage: Apply smoothly on the entire face in the morning and night.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage & administration: Take an adequate amount of this product.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-138809467660107GTIN-13: 8809467660107
EAN-13: 8809467660107
GTIN storage (14 digits): 08809467660107
cellpium premiumex hybrid eye contour carton.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70506-150-012023-06-28C16284748780-19d75b9d1-0ea0-f424-e053-dadaa90a57ce2e4fa0cb-4b22-4510-864d-c42a6702cfb8
70506-150-012020-01-31C16284748780-19d75b9d1-0ea0-f424-e053-dadaa90a57ce2e4fa0cb-4b22-4510-864d-c42a6702cfb8

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
70506-15070506-150-01

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
32d79340-e585-422c-812f-65a26739a2a92e4fa0cb-4b22-4510-864d-c42a6702cfb82023-06-28WarningsExact identifier
spl set id: 2e4fa0cb-4b22-4510-864d-c42a6702cfb8

Reported adverse events (FAERS/openFDA)#

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