FDA.reportPublic FDA data

Kay Chemical Hand Sanitizer Foam

Product NDC
63146-309
Requested package NDC
63146-309-13
11-digit product format
631460309
Labeler code
63146
Product ID
63146-309_725a8b11-6046-4fd5-88b6-731a2599734a
Type
HUMAN OTC DRUG
Nonproprietary name
Ethyl Alcohol
Dosage form
SOLUTION
Route
TOPICAL
Labeler
Kay Chemical
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-04-23
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
55 g/100g
NDC exclude flag
No
Listing certified through
2023-12-31
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 packagepackage63146-30963146-309-13DDiscontinued by firm2026-10-21

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63146-309-132024-01-30C16284748780-11030e365-5248-111a-e063-dadaa90a10e2Drug Facts

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63146-309KAY CHEMICAL HAND SANITIZER FOAM (ETHYL ALCOHOL) SOLUTION [KAY CHEMICAL]4Legacy NDC20240704_981405a0-ba34-4aa0-b0a8-d74cd2427dd1.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63146-309-1363146030913425 g in 1 CAN (63146-309-13) 425 g2020-04-230000-00-00NoNoCurrent