FDA.reportPublic FDA data

Hand Sanitizer

Product NDC
50814-051
11-digit product format
508140051
Labeler code
50814
Product ID
50814-051_a5f0cc00-a838-0aeb-e053-2995a90ae63b
Type
HUMAN OTC DRUG
Nonproprietary name
ALCOHOL
Dosage form
GEL
Route
TOPICAL
Labeler
GFA Production (Xiamen) Co., Ltd.
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-03-01
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
1 mL/mL
NDC exclude flag
No
Listing certified through
2021-12-31
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 productproduct50814-051DDiscontinued by firm2026-09-14
excluded packagepackage50814-05150814-051-02DDiscontinued by firm2026-09-14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50814-051HAND SANITIZER (ALCOHOL) GEL [GFA PRODUCTION (XIAMEN) CO., LTD.]3Legacy NDC20241011_fb672553-3731-43e3-a8ba-f39fc5503614.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50814-051-0250814005102200 mL in 1 BOTTLE (50814-051-02) 200 ml2020-03-010000-00-00NoNoCurrent