FDA.reportPublic FDA data

ANTIBACTERIAL HAND SANITIZER

Manufacturer
Xi'an Explution Tech Co.,Ltd.
Effective date
2020-04-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:09:33

Label at a glance#

ProductANTIBACTERIAL HAND SANITIZER
Active ingredientBENZALKONIUM CHLORIDE
Label structure5 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

benzalkonium chloride(1.2G/L)

USAGE

INDICATIONS & USAGE SECTION

Pump foam and rub hands together briskly until dry.No need to rinse off.

WARNINGS

WARNINGS SECTION

Keep in dry and cool, Do not swallow.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water,glycerinum, COCOGLYCERIDES.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50 ml label50 ml label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75709-004-012021-07-23C16284748780-1c7ccaba7-25a1-fd44-e053-dadaa90aa01bANTIBACTERIAL HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75709-004-01ANTIBACTERIAL HAND SANITIZER50 mL in 1 BOTTLELIQUID501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75709-004ANTIBACTERIAL HAND SANITIZER LIQUID [XI'AN EXPLUTION TECH CO.,LTD.]1Legacy NDC, 1 package rows20200505_a48080c2-bd54-c454-e053-2a95a90a908d.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75709-00475709-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
COCO-GLYCERIDESISE9I7DNUGIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT

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
a4800132-8233-415d-e053-2995a90ac106a48080c2-bd54-c454-e053-2a95a90a908d2020-04-30WarningsExact identifier
spl id: a4800132-8233-415d-e053-2995a90ac106
spl set id: a48080c2-bd54-c454-e053-2a95a90a908d

Reported adverse events (FAERS/openFDA)#

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