Home NDC 74913-778-01 Hand Sanitize
Product NDC 74913-778
Requested package NDC 74913-778-01
11-digit product format 749130778
Labeler code 74913
Product ID 74913-778_a51ce132-6782-5198-e053-2a95a90af9cd
Type HUMAN OTC DRUG
Nonproprietary name Alcohol
Dosage form GEL
Route TOPICAL
Labeler SHANTOU S.E.Z BAOJIE INDUSTRY CO., LTD
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-04-10
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 74913-778-01 Hand Sanitize 2000 mL in 1 BOTTLE, PLASTIC GEL 2000 2 74913-778-16 Hand sanitize 30 mL in 1 BOTTLE, PLASTIC GEL 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 74913-778 HAND SANITIZE (ALCOHOL) GEL [SHANTOU S.E.Z BAOJIE INDUSTRY CO., LTD] 2 Legacy NDC, 1 package rows 20200509_a52089a0-f18c-c797-e053-2a95a90a7840.zip 74913-778 HAND SANITIZE (ALCOHOL) GEL [SHANTOU S.E.Z BAOJIE INDUSTRY CO., LTD] 2 Legacy NDC, 1 package rows 20200509_a51c9aed-0f2b-b6ef-e053-2995a90adc91.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 74913-778-01 74913077801 2000 mL in 1 BOTTLE, PLASTIC (74913-778-01) 2000 ml 2020-04-10 0000-00-00 No No Current