luobenqing Surgical hand sanitizer

Manufacturer
LUSTRE Pharmaceutical Lab.Co.,Ltd.
Effective date
2020-04-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:05:27

Label at a glance#

Productluobenqing Surgical hand sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

please washandbrushyour hands as usual, and dry with a sterile towel (soapresidual prohibited).

Then take 5ml or more of this product and knead for 5 minutes.

DOSAGE & ADMINISTRATION SECTION

surgical hand washing and sterilization in hospltals.

INACTIVE INGREDIENT SECTION

water

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride

OTC - PURPOSE SECTION

Disinfection
Sterilization
No Rinseing

WARNINGS SECTION

This is a sanitizer for external use, and should not be taken orally.

Please keep it out of reach of children.
Miding wilth soap, washing powder or other anlonic detergents should be prohiblited.
Term ofvalidity: 24 months.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
53042-001-012022-01-28C16284748780-1d6a99b39-a2cc-a426-e053-dadaa90af4c2a2126da0-d98b-f931-e053-2995a90a5070

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53042-001-01luobenqing Surgical hand sanitizer150 mL in 1 BOTTLELIQUID1502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53042-001LUOBENQING SURGICAL HAND SANITIZER (SURGICAL HAND SANITIZER) LIQUID [LUSTRE PHARMACEUTICAL LAB.CO.,LTD.]2Legacy NDC, 1 package rows20200409_a2126da0-d98b-f931-e053-2995a90a5070.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53042-00153042-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT

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
a2c93097-a64a-b2af-e053-2a95a90a2eada2126da0-d98b-f931-e053-2995a90a50702020-04-08WarningsExact identifier
spl id: a2c93097-a64a-b2af-e053-2a95a90a2ead
spl set id: a2126da0-d98b-f931-e053-2995a90a5070

Reported adverse events (FAERS/openFDA)#

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