Home NDC 75234-237-06 Hand Sanitizer
Product NDC 75234-237
Requested package NDC 75234-237-06
11-digit product format 752340237
Labeler code 75234
Product ID 75234-237_a324f6f7-a847-270d-e053-2a95a90a6233
Type HUMAN OTC DRUG
Nonproprietary name Alcohol
Dosage form GEL
Route TOPICAL
Labeler Shantou Aoxiangqi Daily Chemical Co., Ltd.
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-04-09
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 · 19 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…2021-12-27 23:28 UTC · source 2021-12-27 8dfbde2a14a4…c9ff85d89658…
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 75234-237-01 Hand Sanitizer 60 mL in 1 BOTTLE GEL 60 1 75234-237-02 Hand Sanitizer 100 mL in 1 BOTTLE GEL 100 1 75234-237-03 Hand Sanitizer 250 mL in 1 BOTTLE GEL 250 1 75234-237-04 Hand Sanitizer 300 mL in 1 BOTTLE GEL 300 1 75234-237-05 Hand Sanitizer 500 mL in 1 BOTTLE GEL 500 1 75234-237-06 Hand Sanitizer 800 mL in 1 BOTTLE GEL 800 1 75234-237-07 Hand Sanitizer 1000 mL in 1 BOTTLE GEL 1000 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 75234-237 HAND SANITIZER (ALCOHOL) GEL [SHANTOU AOXIANGQI DAILY CHEMICAL CO., LTD.] 1 Legacy NDC, 7 package rows 20200415_a32500e9-ef7c-2a77-e053-2995a90a9d32.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 75234-237-06 75234023706 800 mL in 1 BOTTLE (75234-237-06) 800 ml 2020-04-09 0000-00-00 No No Current