Microsure Hand Sanitizer

Product NDC
72513-000
Requested package NDC
72513-000-02
11-digit product format
725130000
Labeler code
72513
Product ID
72513-000_efcf7ca9-a38c-323a-e053-2995a90a83fc
Type
HUMAN OTC DRUG
Nonproprietary name
BENZALKONIUM CHLORIDE
Dosage form
SOLUTION
Route
TOPICAL
Labeler
Strategia Project Management, Inc.
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-07-20
Marketing end
0000-00-00
Substance
BENZALKONIUM CHLORIDE
Active strength
1 mg/mL
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage72513-00072513-000-02IInactivated by FDA2026-10-12

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 3 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage72513-00072513-000-02EExcluded after deficient or non-compliant submission was not correctedexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2022-04-09 23:13 UTC · source 2022-04-08excluded packagepackage72513-00072513-000-02IInactivated by FDAexcluded / ndc_excluded.zip86f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01excluded packagepackage72513-00072513-000-02IInactivated by FDAexcluded / ndc_excluded.zipbd6a592717d7…303034d00443…

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72513-000-01Microsure Hand Sanitizer29.57 mL in 1 BOTTLESOLUTION29.575
72513-000-02Microsure Hand Sanitizer59.14 mL in 1 BOTTLESOLUTION59.145
72513-000-03Microsure Hand Sanitizer1000 mL in 1 BOTTLESOLUTION10005
72513-000-04Microsure Hand Sanitizer3785.41 mL in 1 JUGSOLUTION3785.415
72513-000-05Microsure Hand Sanitizer208198 mL in 1 DRUMSOLUTION2081985
72513-000-06Microsure Hand Sanitizer1040988.2 mL in 1 CONTAINERSOLUTION1040988.25
72513-000-07Microsure Hand Sanitizer1249185.9 mL in 1 CONTAINERSOLUTION1249185.95

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72513-000MICROSURE HAND SANITIZER (BENZALKONIUM CHLORIDE) SOLUTION [STRATEGIA PROJECT MANAGEMENT, INC.]5Legacy NDC, 7 package rows20231221_ab31074e-975a-1c93-e053-2a95a90a3824.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1049254benzalkonium chloride 0.13 % Topical SolutionPSNab31074e-975a-1c93-e053-2a95a90a38245
1049254benzalkonium chloride 1.3 MG/ML Topical SolutionSCDab31074e-975a-1c93-e053-2a95a90a38245
1049254benzalkonium chloride 0.13 % Topical SolutionSYab31074e-975a-1c93-e053-2a95a90a38245

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72513-000-027251300000259.14 mL in 1 BOTTLE (72513-000-02) 59.14 ml2020-07-200000-00-00NoNoCurrent