PURELL Healthcare HEALTHY SP 0.5pct PCMX Antimicrobial Foam

Product NDC
21749-522
Requested package NDC
21749-522-89
11-digit product format
217490522
Labeler code
21749
Product ID
21749-522_31cf7122-71f5-4ab4-983c-8bf4298a10a6
Type
HUMAN OTC DRUG
Nonproprietary name
Chloroxylenol
Dosage form
LIQUID
Route
TOPICAL
Labeler
GOJO Industries, Inc.
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2017-07-14
Marketing end
0000-00-00
Substance
CHLOROXYLENOL
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 packagepackage21749-52221749-522-89DDiscontinued by firm2026-10-02

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
21749-522PURELL HEALTHCARE HEALTHY SP 0.5PCT PCMX ANTIMICROBIAL FOAM (CHLOROXYLENOL) LIQUID [GOJO INDUSTRIES, INC.]2Legacy NDC20241211_bd4682ce-6cc3-4e4c-9e64-b8ffb4ec7835.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
21749-522-89217490522891200 mL in 1 PACKAGE (21749-522-89) 1200 ml2017-07-140000-00-00NoNoCurrent