luobenqing HAND SANITIZER

Product NDC
53042-003
11-digit product format
530420003
Labeler code
53042
Product ID
53042-003_a2da64a5-de32-af8e-e053-2995a90ae453
Type
HUMAN OTC DRUG
Nonproprietary name
HAND SANITIZER
Dosage form
LIQUID
Route
EXTRACORPOREAL
Labeler
LUSTRE Pharmaceutical Lab.Co.,Ltd.
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-03-30
Marketing end
0000-00-00
Substance
ALCOHOL; BENZALKONIUM CHLORIDE
Active strength
105 mL/150mL; mg/150mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

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

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
2286262ethanol 70 % / benzalkonium chloride 0.13 % Topical SolutionPSNa2129f2c-1cd0-2430-e053-2a95a90a98193
2286262benzalkonium chloride 1.3 MG/ML / ethanol 0.7 ML/ML Topical SolutionSCDa2129f2c-1cd0-2430-e053-2a95a90a98193
2286262benzalkonium chloride 0.13 % / ethanol 70 % Topical SolutionSYa2129f2c-1cd0-2430-e053-2a95a90a98193

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
53042-003-0153042000301150 mL in 1 BOTTLE (53042-003-01) 150 ml2020-03-300000-00-00NoNoCurrent