PURELL Professional HEALTHY SP 0.5pct BAK Antimicrobial Foam

Product NDC
21749-685
Requested package NDC
21749-685-90
11-digit product format
217490685
Labeler code
21749
Product ID
21749-685_f942f4be-1bb5-4801-af28-54515333d9f0
Type
HUMAN OTC DRUG
Nonproprietary name
Benzalkonium Chloride
Dosage form
LIQUID
Route
TOPICAL
Labeler
GOJO Industries, Inc.
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2017-10-15
Marketing end
0000-00-00
Substance
BENZALKONIUM CHLORIDE
Active strength
0 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 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage21749-68521749-685-90DDiscontinued by firm2026-10-05

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
21749-685PURELL PROFESSIONAL HEALTHY SP 0.5PCT BAK ANTIMICROBIAL FOAM (BENZALKONIUM CHLORIDE) LIQUID [GOJO INDUSTRIES, INC.]3Legacy NDC20241215_491bef5b-1073-4939-aff0-e0420e3b0098.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
21749-685-90217490685901250 mL in 1 PACKAGE (21749-685-90) 1250 ml2018-04-020000-00-00NoNoCurrent