FDA.reportPublic FDA data

Foaming Instant Hand Sanitizer

Product NDC
72234-457
11-digit product format
722340457
Labeler code
72234
Product ID
72234-457_220dba72-7664-4aa8-ad24-fe210cb27b28
Type
HUMAN OTC DRUG
Nonproprietary name
BENZEALKONIUM CHLORIDE
Dosage form
LIQUID
Route
TOPICAL
Labeler
Pro Source Distributors, Inc.
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2018-05-29
Marketing end
0000-00-00
Substance
BENZALKONIUM CHLORIDE
Active strength
1 mg/mL
NDC exclude flag
No
Listing certified through
2020-12-31
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 · 5 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct72234-457DDiscontinued by firm2026-10-05
excluded packagepackage72234-45772234-457-10DDiscontinued by firm2026-10-05
excluded packagepackage72234-45772234-457-12DDiscontinued by firm2026-10-05
excluded packagepackage72234-45772234-457-14DDiscontinued by firm2026-10-05
excluded packagepackage72234-45772234-457-18DDiscontinued by firm2026-10-05

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 · 5 matching rows.

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

Dataset, Scope, Package NDC table
DatasetScopePackage NDC
excluded productproduct
excluded packagepackage72234-457-10
excluded packagepackage72234-457-12
excluded packagepackage72234-457-18
excluded packagepackage72234-457-14

Reported adverse events (FAERS/openFDA)#

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

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72234-457FOAMING INSTANT HAND SANITIZER (BENZEALKONIUM CHLORIDE) LIQUID [PRO SOURCE DISTRIBUTORS, INC.]1Legacy NDC20190205_f00806de-c7a5-4ed4-a3a8-1066803ba7db.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72234-457-10722340457101000 mL in 1 CARTRIDGE (72234-457-10) 1000 ml2019-02-040000-00-00NoNoCurrent
72234-457-12722340457121000 mL in 1 BAG (72234-457-12) 1000 ml2019-02-040000-00-00NoNoCurrent
72234-457-14722340457143785 mL in 1 BOTTLE, PLASTIC (72234-457-14) 3785 ml2019-02-040000-00-00NoNoCurrent
72234-457-187223404571850 mL in 1 BOTTLE, PLASTIC (72234-457-18) 50 ml2019-02-040000-00-00NoNoCurrent