8HD Hand and Skin Sanitizer

Product NDC
72513-200
Requested package NDC
72513-200-02
11-digit product format
725130200
Labeler code
72513
Product ID
72513-200_b68a4cf8-0215-7dad-e053-2a95a90a04f5
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
2020-12-16
Marketing end
0000-00-00
Substance
BENZALKONIUM CHLORIDE
Active strength
0 g/100mL
NDC exclude flag
No
Listing certified through
2021-12-31
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 packagepackage72513-20072513-200-02IInactivated 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 · 4 matching rows.

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

Captured / source date, Code, Status table
Captured / source dateCodeStatusSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05EExcluded after deficient or non-compliant submission was not correctedd630ba8d3edf…732f749b63fb…
2022-08-30 03:57 UTC · source 2022-08-29IInactivated by FDAfb8cb913e6d1…eb8c232b6be0…
2022-04-09 23:13 UTC · source 2022-04-08IInactivated by FDA86f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01IInactivated by FDAbd6a592717d7…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
72513-200-018HD Hand and Skin Sanitizer29.57 mL in 1 BOTTLELIQUID29.572
72513-200-028HD Hand and Skin Sanitizer59.14 mL in 1 BOTTLELIQUID59.142
72513-200-038HD Hand and Skin Sanitizer1000 mL in 1 BOTTLELIQUID10002
72513-200-048HD Hand and Skin Sanitizer3785.41 mL in 1 JUGLIQUID3785.412
72513-200-058HD Hand and Skin Sanitizer208198 mL in 1 DRUMLIQUID2081982
72513-200-068HD Hand and Skin Sanitizer1040988.2 mL in 1 CONTAINERLIQUID1040988.22
72513-200-078HD Hand and Skin Sanitizer1249185.9 mL in 1 CONTAINERLIQUID1249185.92

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72513-2008HD HAND AND SKIN SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [STRATEGIA PROJECT MANAGEMENT, INC.]2Legacy NDC, 7 package rows20231221_b68a4cf8-0214-7dad-e053-2a95a90a04f5.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1049254benzalkonium chloride 0.13 % Topical SolutionPSNb68a4cf8-0214-7dad-e053-2a95a90a04f52
1049254benzalkonium chloride 1.3 MG/ML Topical SolutionSCDb68a4cf8-0214-7dad-e053-2a95a90a04f52
1049254benzalkonium chloride 0.13 % Topical SolutionSYb68a4cf8-0214-7dad-e053-2a95a90a04f52

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72513-200-027251302000259.14 mL in 1 BOTTLE (72513-200-02) 59.14 ml2020-12-160000-00-00NoNoCurrent