FDA.reportPublic FDA data

JEJUON DailyCare Handwash

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 DailyCare Handwash
Active ingredientBENZALKONIUM CHLORIDE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

handwash tubehandwash tube

OTC - ACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT SECTION

OTC - DO NOT USE SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - PURPOSE SECTION

OTC - STOP USE SECTION

OTC - WHEN USING SECTION

OTHER SAFETY INFORMATION

WARNINGS AND PRECAUTIONS SECTION

DOSAGE & ADMINISTRATION SECTION

WARNINGS SECTION

INDICATIONS & USAGE SECTION

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1233282benzalkonium chloride 0.1 % Medicated Liquid SoapPSN1
1233282benzalkonium chloride 1 MG/ML Medicated Liquid SoapSCD1
1233282benzalkonium chloride 0.1 % Medicated Liquid SoapSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76744-150-012023-01-30C16284748780-1f386c64a-20bc-0266-e053-dadaa90a7c1aJEJUON DailyCare Handwash : Tube: 76744-150-01

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76744-150-01JEJUON DailyCare Handwash50 mL in 1 TUBELIQUID501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76744-150JEJUON DAILYCARE HANDWASH (BENZALKONIUM CHLORIDE) LIQUID [KOREA BEAUTY INDUSTRY DEVELOPMENT INSTITUTE CO.,LTD.]1Legacy NDC, 1 package rows20200509_a5101886-5664-165c-e053-2a95a90a496f.zip

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76744-15076744-150-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
GLYCERINPDC6A3C0OXIACT
SODIUM LAURYL SULFATE368GB5141JIACT
LAVANDULA ANGUSTIFOLIA FLOWERING TOP9YT4B71U8PIACT
LIME OILUZH29XGA8GIACT
TURMERIC856YO1Z64FIACT
HYALURONATE SODIUMYSE9PPT4THIACT
JUNIPERUS DEPPEANA WOOD OIL4739QA5686IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
PHENOXYETHANOLHIE492ZZ3TIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
TANGERINEKH3E3096OOIACT
NELUMBO NUCIFERA LEAF60C608DPVTIACT
ROSEMARYIJ67X351P9IACT
ORANGE OILAKN3KSD11BIACT
XANTHAN GUMTTV12P4NEEIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
SODIUM CHLORIDE451W47IQ8XIACT
WATER059QF0KO0RIACT
DISODIUM COCOAMPHODIACETATE18L9G3U51MIACT
POTASSIUM COCOYL GLYCINATEWZ70FUF22UIACT
EUCALYPTUS OIL2R04ONI662IACT
LAVANDIN OIL9RES347CKGIACT
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
a5101886-5665-165c-e053-2a95a90a496fa5101886-5664-165c-e053-2a95a90a496f2020-05-07Exact identifier
spl id: a5101886-5665-165c-e053-2a95a90a496f
spl set id: a5101886-5664-165c-e053-2a95a90a496f

Reported adverse events (FAERS/openFDA)#

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