Microsure Hand and Skin Sanitizer

Product NDC
72513-300
Requested package NDC
72513-300-07
11-digit product format
725130300
Labeler code
72513
Product ID
72513-300_efdf4b5b-4caa-2b09-e053-2a95a90aa375
Type
HUMAN OTC DRUG
Nonproprietary name
BENZALKONIUM CHLORIDE
Dosage form
LIQUID
Route
TOPICAL
Labeler
Strategia Project Management, Inc.
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-12-21
Marketing end
0000-00-00
Substance
BENZALKONIUM CHLORIDE
Active strength
0 g/100mL
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 packagepackage72513-30072513-300-07IInactivated by FDA2026-10-05

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 · 1 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 packagepackage72513-30072513-300-07EExcluded after deficient or non-compliant submission was not correctedexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…

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
72513-300-01Microsure Hand and Skin Sanitizer29.57 mL in 1 BOTTLELIQUID29.574
72513-300-02Microsure Hand and Skin Sanitizer59.14 mL in 1 BOTTLELIQUID59.144
72513-300-03Microsure Hand and Skin Sanitizer1000 mL in 1 BOTTLELIQUID10004
72513-300-04Microsure Hand and Skin Sanitizer3785.41 mL in 1 JUGLIQUID3785.414
72513-300-05Microsure Hand and Skin Sanitizer208198 mL in 1 DRUMLIQUID2081984
72513-300-06Microsure Hand and Skin Sanitizer1040988.2 mL in 1 CONTAINERLIQUID1040988.24
72513-300-07Microsure Hand and Skin Sanitizer1249185.9 mL in 1 CONTAINERLIQUID1249185.94
72513-300-08Microsure Hand and Skin Sanitizer946 mL in 1 BOTTLELIQUID9464

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72513-300MICROSURE HAND AND SKIN SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [STRATEGIA PROJECT MANAGEMENT, INC.]4Legacy NDC, 8 package rows20231221_b6ffa0cd-a474-3929-e053-2995a90a0b65.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1049254benzalkonium chloride 0.13 % Topical SolutionPSNb6ffa0cd-a474-3929-e053-2995a90a0b654
1049254benzalkonium chloride 1.3 MG/ML Topical SolutionSCDb6ffa0cd-a474-3929-e053-2995a90a0b654
1049254benzalkonium chloride 0.13 % Topical SolutionSYb6ffa0cd-a474-3929-e053-2995a90a0b654

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72513-300-07725130300071249185.9 mL in 1 CONTAINER (72513-300-07) 1249185.9 ml2020-12-210000-00-00NoNoCurrent