luobenqing HAND SANITIZER

Manufacturer
LUSTRE Pharmaceutical Lab.Co.,Ltd.
Effective date
2020-04-09
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:05:37

Label at a glance#

Productluobenqing HAND SANITIZER
Active ingredientALCOHOL, BENZALKONIUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Flammable out of fire.

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1 3%w/v
Denatured Alcohol 23A 70%v/v

INACTIVE INGREDIENT SECTION

water

OTC - PURPOSE SECTION

Disinfection
Sterilization
No Rinseing

INDICATIONS & USAGE SECTION

Use appropriate amount on palm and rubbing few minutes.

WARNINGS SECTION

Keep reach out of children.
Flammable out of fire.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2286262ethanol 70 % / benzalkonium chloride 0.13 % Topical SolutionPSN3
2286262benzalkonium chloride 1.3 MG/ML / ethanol 0.7 ML/ML Topical SolutionSCD3
2286262benzalkonium chloride 0.13 % / ethanol 70 % Topical SolutionSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
53042-003-012022-01-28C16284748780-1d6a99b39-54bb-a426-e053-dadaa90af4c2a2129f2c-1cd0-2430-e053-2a95a90a9819

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53042-003-01luobenqing HAND SANITIZER150 mL in 1 BOTTLELIQUID1503

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53042-003LUOBENQING HAND SANITIZER (HAND SANITIZER) LIQUID [LUSTRE PHARMACEUTICAL LAB.CO.,LTD.]3Legacy NDC, 1 package rows20200410_a2129f2c-1cd0-2430-e053-2a95a90a9819.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
53042-00353042-003-01

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
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
a2da64a5-de32-af8e-e053-2995a90ae453a2129f2c-1cd0-2430-e053-2a95a90a98192020-04-09WarningsExact identifier
spl id: a2da64a5-de32-af8e-e053-2995a90ae453
spl set id: a2129f2c-1cd0-2430-e053-2a95a90a9819

Reported adverse events (FAERS/openFDA)#

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