FDA.reportPublic FDA data

Hand Sanitizer

Product NDC
76924-000
Requested package NDC
76924-000-00
11-digit product format
769240000
Labeler code
76924
Product ID
76924-000_a5137f5b-a84d-9be5-e053-2a95a90af01a
Type
HUMAN OTC DRUG
Nonproprietary name
ALCOHOL
Dosage form
GEL
Route
TOPICAL
Labeler
General Organics Inc.
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-04-01
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 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage76924-00076924-000-00IInactivated by FDA2026-10-05

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 3 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage76924-00076924-000-00IInactivated by FDAexcluded / ndc_excluded.zipf5e01cc5f278…a2eaf40c39c3…
2024-05-15 03:39 UTC · source 2024-05-14excluded packagepackage76924-00076924-000-00IInactivated by FDAexcluded / ndc_excluded.zip834df4deac94…adcc014656a3…
2024-03-11 06:39 UTC · source 2024-03-08excluded packagepackage76924-00076924-000-00IInactivated by FDAexcluded / ndc_excluded.zip1332a3947898…d4bfe170f9cd…

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
EffectiveRelated label
2025-08-26Hand Sanitizer
2025-07-29Hand Sanitizer
2024-05-24Hand Sanitizer
2024-01-30Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76924-000-00Hand Sanitizer236 mL in 1 BOTTLEGEL2363

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76924-000HAND SANITIZER (ALCOHOL) GEL [GENERAL ORGANICS INC.]3Legacy NDC, 1 package rows20240525_f34e6823-1ef0-49ff-9379-8c818d6d57d6.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
581662ethanol 70 % Topical GelPSNf34e6823-1ef0-49ff-9379-8c818d6d57d63
581662ethanol 0.7 ML/ML Topical GelSCDf34e6823-1ef0-49ff-9379-8c818d6d57d63
581662ethanol 70 % Topical GelSYf34e6823-1ef0-49ff-9379-8c818d6d57d63
581662ethyl alcohol 70 % Topical GelSYf34e6823-1ef0-49ff-9379-8c818d6d57d63

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
76924-000-0076924000000236 mL in 1 BOTTLE (76924-000-00) 236 ml2020-04-010000-00-00NoNoCurrent