Home NDC 80666-555-50 Phoenix Hand Sanitizer Gel
Product NDC 80666-555
Requested package NDC 80666-555-50
11-digit product format 806660555
Labeler code 80666
Product ID 80666-555_1224bc76-eaf8-4676-934e-0f1db8fe725a
Type HUMAN OTC DRUG
Nonproprietary name Ethyl alcohol
Dosage form GEL
Route TOPICAL
Labeler THANH CONG PHARMACEUTICAL AND TRADING CO.,LTD
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-10-01
Marketing end 0000-00-00
Substance ALCOHOL
Active strength 70 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 80666-555-50 Phoenix Hand Sanitizer Gel 1000 mL in 1 BOTTLE GEL 1000 1 80666-555-55 Phoenix Hand Sanitizer Gel 500 mL in 1 BOTTLE GEL 500 1 80666-555-56 Phoenix Hand Sanitizer Gel 3800 mL in 1 CAN GEL 3800 1 80666-555-58 Phoenix Hand Sanitizer Gel 5000 mL in 1 CAN GEL 5000 1 80666-555-80 Phoenix Hand Sanitizer Gel 250 mL in 1 BOTTLE GEL 250 1 80666-555-85 Phoenix Hand Sanitizer Gel 100 mL in 1 BOTTLE GEL 100 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 80666-555 PHOENIX HAND SANITIZER GEL (ETHYL ALCOHOL) GEL [THANH CONG PHARMACEUTICAL AND TRADING CO.,LTD] 1 Legacy NDC, 6 package rows 20201007_f1153eee-b624-407d-bd2c-2ba864356a63.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 80666-555-50 80666055550 1000 mL in 1 BOTTLE (80666-555-50) 1000 ml 2020-10-01 0000-00-00 No No Current