Cellpium premiumEX hybrid yoon

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 01:27:58

Label at a glance#

ProductCellpium premiumEX hybrid yoon
Active ingredientDIMETHICONE
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: DIMETHICONE 2.08%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: WATER, CAPRYLIC/CAPRIC TRIGLYCERIDE, PENTAERYTHRITYL TETRAETHYLHEXANOATE, GLYCERIN, MACADAMIA TERNIFOLIA SEED OIL, CETEARYL ALCOHOL, BUTYROSPERMUM PARKII (SHEA) BUTTER, NIACINAMIDE, BIFIDA FERMENT LYSATE, GLYCERYL STEARATE, PEG-100 STEARATE, DIOSCOREA JAPONICA ROOT EXTRACT, BEESWAX, METHYLPROPANEDIOL, MYRISTYL ALCOHOL, POLYSORBATE 60, PIPER METHYSTICUM LEAF/ROOT/STEM EXTRACT, 1,2-HEXANEDIOL, HUMAN CORD BLOOD CELL CONDITIO NED MEDIA, TRANEXAMIC ACID, ZEA MAYS (CORN) STARCH, HYDROGENATED LECITHIN, SOLUBLE COLLAGEN, PHENOXYETHANOL, TOCOPHERYL ACETATE, PHELLODENDRON AMURENSE BARK EXTRACT, ARCTIUM LAPPA ROOT EXTRACT, PHELLINUS LINTEUS EXTRACT, BUTYLENE GLYCOL, XANTHAN GUM, ARGANIA SPINOSA KERNEL OIL, ETHYLHEXYLGLYCERIN, POLYQUATERNIUM-51, PORTULACA OLERACEA EXTRACT, PUERARIA THUNBERGIANA ROOT EXTRACT, CNIDIUM OFFICINALE ROOT EXTRACT, GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT, PAEONIA LACTIFLORA ROOT EXTRACT, OLEA EUROPAEA (OLIVE) LEAF EXTRACT, NYMPHAEA ALBA FLOWER EXTRACT, GLYCOSYL TREHALOSE, HYDROGENATED POLYISOBUTENE, SQUALANE, ALCOHOL, FRAGRANCE, HYDROGENATED STARCH HYDROLYSATE, RAFFINOSE, ADENOSINE, BIOSACCHARIDE GUM-1, ALOE BARBADENSIS LEAF JUICE, ISONONYL ISONONANOATE, POLYGLYCERYL-10 STEARATE, NELUMBO NUCIFERA CALLUS CULTURE EXTRACT, BISABOLOL, LECITHIN, POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE, STEARIC ACID, PANTHENOL, ASCORBYL GLUCOSIDE, ZINC PCA, GLYCERYL STEARATE SE, SORBITAN STEARATE, CERAMIDE NP, SODIUM HYALURONATE, CARBOMER, DISODIUM EDTA, JOJOBA ESTERS, CHOLESTEROL, PENTYLENE GLYCOL, DIPROPYLENE GLYCOL, CARAMEL, HYDROLYZED AVOCADO PROTEIN, MALTODEXTRIN, POLYSORBATE 20, FOLIC ACID, DICAPRYLYL CARBONATE, INULIN LAURYL CARBAMATE, PROPYLENE GLYCOL, SODIUM PALMITOYL PROLINE, SUCROSE DISTEARATE, ACETIC ACID, LACTIC ACID, ACACIA SENEGAL GUM, DISODIUM STEAROYL GLUTAMATE, TROMETHAMINE, GENISTEIN METHYL ETHER, PALMITOYL TRIPEPTIDE-5, PALMITOYL PENTAPEPTIDE-4, POTASSIUM SORBATE

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-138809467660121GTIN-13: 8809467660121
EAN-13: 8809467660121
GTIN storage (14 digits): 08809467660121
cellpium premiumex hybrid yoon carton.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70506-160-012023-06-28C16284748780-19d75b9d0-3235-f424-e053-dadaa90a57ceda76d740-c0c7-4d2d-ba3f-2dad18efb6cc
70506-160-012020-01-31C16284748780-19d75b9d0-3235-f424-e053-dadaa90a57ceda76d740-c0c7-4d2d-ba3f-2dad18efb6cc

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
70506-16070506-160-01

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
6508391d-6450-4117-a86a-efe52ecd6ef4da76d740-c0c7-4d2d-ba3f-2dad18efb6cc2023-06-28WarningsExact identifier
spl set id: da76d740-c0c7-4d2d-ba3f-2dad18efb6cc

Reported adverse events (FAERS/openFDA)#

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