FDA.reportPublic FDA data

Retail Hand Sanitizer

Product NDC
63146-311
11-digit product format
631460311
Labeler code
63146
Product ID
63146-311_09d1eae5-25cc-4e71-af58-b0709f37f524
Type
HUMAN OTC DRUG
Nonproprietary name
Alcohol
Dosage form
LIQUID
Route
TOPICAL
Labeler
Kay Chemical Company
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-09-10
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
60 mL/100mL
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 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct63146-311DDiscontinued by firm2026-08-17
excluded packagepackage63146-31163146-311-09DDiscontinued by firm2026-08-17

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63146-311RETAIL HAND SANITIZER (ALCOHOL) LIQUID [KAY CHEMICAL COMPANY]3Legacy NDC20240823_f9b8fd91-0915-452e-8122-82098599ccdb.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63146-311-09631460311091200 mL in 1 BOTTLE, PLASTIC (63146-311-09) 1200 ml2020-09-100000-00-00NoNoCurrent