Cellpium premiumEX hybrid toner

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 premiumEX hybrid toner
Active ingredientNIACINAMIDE
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: NIACINAMIDE 2.0%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: WATER, BUTYLENE GLYCOL, ALCOHOL, GLYCERIN, PIPER METHYSTICUM LEAF/ROOT/STEM EXTRACT, DIOSCOREA JAPONICA ROOT EXTRACT, 1,2-HEXANEDIOL, HUMAN CORD BLOOD CELL CONDITIO NED MEDIA, BETAINE, SOLUBLE COLLAGEN, HYDROGENATED LECITHIN, PHENOXYETHANOL, CAPRYLIC/CAPRIC TRIGLYCERIDE, ARCTIUM LAPPA ROOT EXTRACT, PHELLINUS LINTEUS EXTRACT, TOCOPHERYL ACETATE, COCETH-7, PPG-1-PEG-9 LAURYL GLYCOL ETHER, ETHYLHEXYLGLYCERIN, PORTULACA OLERACEA EXTRACT, PUERARIA THUNBERGIANA ROOT EXTRACT, CNIDIUM OFFICINALE ROOT EXTRACT, GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT, PAEONIA LACTIFLORA ROOT EXTRACT, PSEUDOALTEROMONAS FERMENT EXTRACT, NELUMBO NUCIFERA CALLUS CULTURE EXTRACT, NYMPHAEA ALBA FLOWER EXTRACT, POLYSORBATE 60, XANTHAN GUM, POLYQUATERNIUM-51, GLYCOSYL TREHALOSE, ADENOSINE, CARBOMER, ALOE BARBADENSIS LEAF JUICE, TROMETHAMINE, DISODIUM EDTA, FRAGRANCE, HYDROGENATED STARCH HYDROLYSATE, RAFFINOSE, BIOSACCHARIDE GUM-1, AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER, PEG-40 HYDROGENATED CASTOR OIL, STEARETH-21, CERAMIDE NP, HYDROLYZED HYALURONIC ACID, LECITHIN, CETYL ALCOHOL, STEARETH-2, ISOHEXADECANE, STEARIC ACID, DIPROPYLENE GLYCOL, CHOLESTEROL, SODIUM HYALURONATE, PENTYLENE GLYCOL, SODIUM PALMITOYL PROLINE, PEG-30 DIPOLYHYDROXYSTEARATE, PPG-26-BUTETH-26, CAPRYLYL GLYCOL, FOLIC ACID, GLYCERYL POLYMETHACRYLATE, ACETYL GLUCOSAMINE, HYALURONIC ACID, HYDROLYZED COLLAGEN, GENISTEIN METHYL ETHER, ASCORBIC ACID, PANTHENOL, PALMITOYL TRIPEPTIDE-5, TRIPEPTIDE-29, COPPER TRIPEPTIDE-1, TRIPEPTIDE-1, ACETYL HEXAPEPTIDE-8, PALMITOYL PENTAPEPTIDE-4, HEXAPEPTIDE-12, HEXAPEPTIDE-9, NICOTINOYL TRIPEPTIDE-35, NONAPEPTIDE-7, PALMITOYL TRIPEPTIDE-1, PALMITOYL TETRAPEPTIDE-7, PALMITOYL TRIPEPTIDE-29

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-138809467660091GTIN-13: 8809467660091
EAN-13: 8809467660091
GTIN storage (14 digits): 08809467660091
cellpium premiumex hybrid toner carton.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70506-140-012023-06-28C16284748780-19d75b9d0-e2b7-f424-e053-dadaa90a57ce4ade4a22-6c97-4424-99f6-a0b167c43520
70506-140-012020-01-31C16284748780-19d75b9d0-e2b7-f424-e053-dadaa90a57ce4ade4a22-6c97-4424-99f6-a0b167c43520

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
70506-14070506-140-01

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
NIACINAMIDE25X51I8RD4ACTIB
WATER059QF0KO0RIACT
BUTYLENE GLYCOL3XUS85K0RAIACT

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
5103e3e7-7ee5-40ee-b227-fe151fef974c4ade4a22-6c97-4424-99f6-a0b167c435202023-06-28WarningsExact identifier
spl set id: 4ade4a22-6c97-4424-99f6-a0b167c43520

Reported adverse events (FAERS/openFDA)#

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