FDA.reportPublic FDA data

ANTI-BACTERIAL HAND Cream

Manufacturer
Natural Korea Co., Ltd.
Effective date
2021-01-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:36:35

Label at a glance#

ProductANTI-BACTERIAL HAND Cream
Active ingredientBENZALKONIUM CHLORIDE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ANTI-BACTERIAL HAND CREAMANTI-BACTERIAL HAND CREAM

OTC - ACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT SECTION

OTC - ASK DOCTOR SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

WARNINGS SECTION

OTC - WHEN USING SECTION

INDICATIONS & USAGE SECTION

OTHER SAFETY INFORMATION

OTC - PURPOSE SECTION

DOSAGE & ADMINISTRATION SECTION

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2371908benzalkonium chloride 0.05 % Topical CreamPSN1
2371908benzalkonium chloride 0.5 MG/ML Topical CreamSCD1
2371908benzalkonium chloride 0.05 % Topical CreamSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
1681bc73-b05f-12c3-1075-382ae39f449cProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74646-0017-12023-01-30C16284748780-1f386c649-a070-0266-e053-dadaa90a7c1aANTI-BACTERIAL HAND CREAM 50 mL 74646-0017-1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74646-0017-1ANTI-BACTERIAL HAND Cream1 in 1 BOXCREAM11
74646-0017-1ANTI-BACTERIAL HAND Cream50 mL in 1 TUBECREAM501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74646-0017ANTI-BACTERIAL HAND CREAM (BENZALKONIUM CHLORIDE) CREAM [NATURAL KOREA CO., LTD.]1Legacy NDC, 2 package rows20210107_b83780d9-887f-117f-e053-2995a90a3284.zip

Products#

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

DailyMed product names page 1 of 1 · 34 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74646-001774646-0017-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 32 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIPROPYLENE GLYCOLE107L85C40IACT
UREA8W8T17847WIACT
MINERAL OILT5L8T28FGPIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
YELLOW WAX2ZA36H0S2VIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
DIMETHICONE92RU3N3Y1OIACT
SORBITAN SESQUIOLEATE0W8RRI5W5AIACT
PEG-100 STEARATEYD01N1999RIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES0C9AC7D6XUIACT
PHENOXYETHANOLHIE492ZZ3TIACT
SALICYLIC ACIDO414PZ4LPZIACT
ARGININE94ZLA3W45FIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
ALLANTOIN344S277G0ZIACT
POLYSORBATE 806OZP39ZG8HIACT
EDETATE DISODIUM7FLD91C86KIACT
ROSA CANINA FRUIT OILCR7307M3QZIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
GRAPEFRUITO82C39RR8CIACT
ALOE VERA LEAFZY81Z83H0XIACT
CETYL ALCOHOL936JST6JCNIACT
STEARIC ACID4ELV7Z65APIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
POLYSORBATE 60CAL22UVI4MIACT
ISOHEXADECANE918X1OUF1EIACT
SOPHORA FLAVESCENS ROOTIYR6K8KQ5KIACT
ROSEMARYIJ67X351P9IACT

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
b83780d9-8880-117f-e053-2995a90a3284b83780d9-887f-117f-e053-2995a90a32842021-01-06Exact identifier
spl id: b83780d9-8880-117f-e053-2995a90a3284
spl set id: b83780d9-887f-117f-e053-2995a90a3284

Reported adverse events (FAERS/openFDA)#

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