FDA.reportPublic FDA data

JEJUON Pure Clean Hand Gel

Manufacturer
Korea Beauty Industry Development Institute Co.,Ltd.
Effective date
2020-05-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:10:22

Label at a glance#

ProductJEJUON Pure Clean Hand Gel
Active ingredientBENZALKONIUM CHLORIDE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

JEJUON Pure Clean Hand GelJEJUON Pure Clean Hand Gel

WARNINGS SECTION

INDICATIONS & USAGE SECTION

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - WHEN USING SECTION

OTC - DO NOT USE SECTION

OTHER SAFETY INFORMATION

INACTIVE INGREDIENT SECTION

DOSAGE & ADMINISTRATION SECTION

OTC - STOP USE SECTION

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1049228benzalkonium chloride 0.1 % Topical GelPSN1
1049228benzalkonium chloride 0.001 MG/MG Topical GelSCD1
1049228benzalkonium chloride 0.1 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76744-250-012023-01-30C16284748780-1f386c64a-0742-0266-e053-dadaa90a7c1aJEJUON Pure Clean Hand Gel: Tube :76744-250-01

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76744-250-01JEJUON Pure Clean Hand Gel50 mL in 1 TUBEGEL501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76744-250JEJUON PURE CLEAN HAND GEL (BENZALKONIUM CHLORIDE) GEL [KOREA BEAUTY INDUSTRY DEVELOPMENT INSTITUTE CO.,LTD.]1Legacy NDC, 1 package rows20200509_a5111eab-55e8-a0bf-e053-2a95a90a34fa.zip

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76744-25076744-250-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ALOE VERA LEAFZY81Z83H0XIACT
TANGERINEKH3E3096OOIACT
GLYCERINPDC6A3C0OXIACT
HONEYY9H1V576FHIACT
EUCALYPTUS OIL2R04ONI662IACT
LAVANDIN OIL9RES347CKGIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
POLYSORBATE 207T1F30V5YHIACT
SODIUM CARBONATE45P3261C7TIACT
NELUMBO NUCIFERA LEAF60C608DPVTIACT
TURMERIC856YO1Z64FIACT
PANTHENOLWV9CM0O67ZIACT
ORANGE OILAKN3KSD11BIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
LAVANDULA ANGUSTIFOLIA FLOWERING TOP9YT4B71U8PIACT
ROSEMARYIJ67X351P9IACT
LIME OILUZH29XGA8GIACT
JUNIPERUS DEPPEANA WOOD OIL4739QA5686IACT
PENTYLENE GLYCOL50C1307PZGIACT
WATER059QF0KO0RIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
HYALURONATE SODIUMYSE9PPT4THIACT

Source Document#

Source XML · Source PDF

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
a5111eab-55e9-a0bf-e053-2a95a90a34faa5111eab-55e8-a0bf-e053-2a95a90a34fa2020-05-07Exact identifier
spl id: a5111eab-55e9-a0bf-e053-2a95a90a34fa
spl set id: a5111eab-55e8-a0bf-e053-2a95a90a34fa

Reported adverse events (FAERS/openFDA)#

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