Home NDC 78792-012-02 ALCOHOL HAND SANITIZER
Product NDC 78792-012
Requested package NDC 78792-012-02
11-digit product format 787920012
Labeler code 78792
Product ID 78792-012_b68ca27d-b801-4aac-e053-2a95a90aa3f9
Type HUMAN OTC DRUG
Nonproprietary name ALCOHOL HAND SANITIZER
Dosage form GEL
Route TOPICAL
Labeler GUANGDONG THEAOSON TECHNOLOGY CO.,LTD
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-03-30
Marketing end 0000-00-00
Substance ALCOHOL
Active strength 75 mL/100mL
NDC exclude flag No
Listing certified through 2021-12-31
Current FDA listing Historical FDA.report record 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 · 18 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…2022-08-30 03:57 UTC · source 2022-08-29 fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 bd6a592717d7…303034d00443…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 78792-012-01 ALCOHOL HAND SANITIZER 50 mL in 1 BOTTLE GEL 50 1 78792-012-02 ALCOHOL HAND SANITIZER 100 mL in 1 BOTTLE GEL 100 1 78792-012-03 ALCOHOL HAND SANITIZER 182 mL in 1 BOTTLE GEL 182 1 78792-012-04 ALCOHOL HAND SANITIZER 478 mL in 1 BOTTLE GEL 478 1 78792-012-05 ALCOHOL HAND SANITIZER 494 mL in 1 BOTTLE GEL 494 1 78792-012-06 ALCOHOL HAND SANITIZER 1000 mL in 1 BOTTLE GEL 1000 1 78792-012-07 ALCOHOL HAND SANITIZER 5000 mL in 1 BOTTLE GEL 5000 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 78792-012 ALCOHOL HAND SANITIZER GEL [GUANGDONG THEAOSON TECHNOLOGY CO.,LTD] 1 Legacy NDC, 7 package rows 20201217_b68cbf9f-37c4-d6aa-e053-2a95a90a4197.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 78792-012-02 78792001202 100 mL in 1 BOTTLE (78792-012-02) 100 ml 2020-03-30 0000-00-00 No No Current