FDA.reportPublic FDA data

Luxury Cell Performance Emulsion

Manufacturer
Pharmicell Co., Ltd.
Effective date
2014-09-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:40:15

Label at a glance#

ProductLuxury Cell Performance Emulsion
Active ingredientALLANTOIN
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredient : ALLANTOIN 0.5%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients : WATER, HYDROGENATED POLYDECENE, BUTYLENE GLYCOL, GLYCERIN, TRIETHYLHEXANOIN, HUMAN BONE MARROW STEM CELL CONDITIONED MEDIA, CITRUS PARADISI (GRAPEFRUIT) FRUIT EXTRACT, BEHENYL ALCOHOL, GLYCERYL STEARATE, PEG-100 STEARATE, BEHENIC ACID, ISOSTEARIC ACID, STEARIC ACID, HYDROGENATED LECITHIN, POLYGONUM MULTIFLORUM ROOT EXTRACT, ARTEMISIA PRINCEPS LEAF EXTRACT, PORTULACA OLERACEA EXTRACT, PANAX GINSENG ROOT EXTRACT, ASPARAGUS COCHINCHINENSIS ROOT EXTRACT, 1,2-HEXANEDIOL, CARBOMER, PHENOXYETHANOL, PEG-5 GLYCERYL STEARATE, GLYCERYL STEARATE SE, POTASSIUM HYDROXIDE, ALTHAEA ROSEA ROOT EXTRACT, ALOE BARBADENSIS LEAF EXTRACT, GANODERMA LUCIDUM (MUSHROOM) EXTRACT, GRIFOLA FRONDOSA EXTRACT, INONOTUS OBLIQUUS (MUSHROOM) EXTRACT, SPARASSIS CRISPA EXTRACT, PHELLINUS LINTEUS EXTRACT , CERAMIDE 3, ADENOSINE, LAVANDULA ANGUSTIFOLIA (LAVENDER) OIL, MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL, EUCALYPTUS GLOBULUS LEAF OIL, GERANIUM MACULATUM OIL, ROSMARINUS OFFICINALIS (ROSEMARY) LEAF OIL, MENTHA PIPERITA (PEPPERMINT) OIL

PURPOSE

OTC - PURPOSE SECTION

Purpose : Skin Protectant

WARNINGS

WARNINGS SECTION

Warnings : Harmful if swallowed. Avoid contact with the eyes. Keep out of reach of children. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.

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

Indication and usage : After using the serum, apply the emulsion to the entire face evenly along the skin texture like massaging the entire face.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage and administration : Take a proper amount of the product, and spread it evenly over the entire face.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-138809287440217GTIN-13: 8809287440217
EAN-13: 8809287440217
GTIN storage (14 digits): 08809287440217		luxury cell performance emulsion carton.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60949-130-012019-11-27C16284748780-19855e2a2-46fb-60a7-e053-dbdaa90a05bd7eab83fb-72a5-4e74-8015-40df3b6465a5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60949-130-01Luxury Cell Performance Emulsion130 mL in 1 CARTONCREAM1301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60949-130LUXURY CELL PERFORMANCE EMULSION (ALLANTOIN) CREAM [PHARMICELL CO., LTD.]1Legacy NDC, 1 package rows20140922_7eab83fb-72a5-4e74-8015-40df3b6465a5.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALLANTOINACTIVE INGREDIENT344S277G0Z1
ALLANTOINACTIVE MOIETY344S277G0Z1
BUTYLENE GLYCOLINACTIVE INGREDIENT3XUS85K0RA1
WATERINACTIVE INGREDIENT059QF0KO0R1

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
60949-13060949-130-01

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
ALLANTOIN344S277G0ZACTIB
WATER059QF0KO0RIACT
BUTYLENE GLYCOL3XUS85K0RAIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
BUTYLENE GLYCOLBUTYLENE GLYCOL3XUS85K0RASYSTEM / TRANSDERMAL8.12 mgExact identifier — unii candidate
2 equally ranked IID candidates
BUTYLENE GLYCOLBUTYLENE GLYCOL3XUS85K0RASYSTEM / TOPICAL1400 mgExact identifier — unii candidate
2 equally ranked IID candidates

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
74318e49-75c9-4d0a-a2d3-bce48ca030fb7eab83fb-72a5-4e74-8015-40df3b6465a52014-09-22WarningsExact identifier
spl id: 74318e49-75c9-4d0a-a2d3-bce48ca030fb
spl set id: 7eab83fb-72a5-4e74-8015-40df3b6465a5

Reported adverse events (FAERS/openFDA)#

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