Kay Actigel

Product NDC
63146-301
Requested package NDC
63146-301-02
11-digit product format
631460301
Labeler code
63146
Product ID
63146-301_54e5052e-23fe-4336-8174-c186cf080af9
Type
HUMAN OTC DRUG
Nonproprietary name
Ethanol
Dosage form
SOLUTION
Route
TOPICAL
Labeler
Kay Chemical Company
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2010-05-26
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
60 mL/100mL
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 packagepackage63146-30163146-301-02DDiscontinued by firm2026-10-15

Reported adverse events (FAERS/openFDA)#

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

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63146-301KAY ACTIGEL (ETHANOL) SOLUTION [KAY CHEMICAL COMPANY]5Legacy NDC20240820_57132d55-4f4a-47dd-993c-2a35a4db72c0.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63146-301-0263146030102800 mL in 1 BAG (63146-301-02) 800 ml2010-05-260000-00-00NoNoCurrent