Home NDC 79644-220-01 Hand Sanitizer
Product NDC 79644-220
Requested package NDC 79644-220-01
11-digit product format 796440220
Labeler code 79644
Product ID 79644-220_c333c252-28f0-0407-e053-2995a90ac18e
Type HUMAN OTC DRUG
Nonproprietary name Hand Sanitizer
Dosage form AEROSOL, FOAM
Route TOPICAL
Labeler Trokar, S.A. de C.V.
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-03-30
Marketing end 0000-00-00
Substance BENZALKONIUM CHLORIDE
Active strength 0 g/100mL
NDC exclude flag No
Listing certified through 2022-12-31
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, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 I Inactivated by FDA 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 I Inactivated by FDA ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 I Inactivated by FDA 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 I Inactivated by FDA 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2022-08-30 03:57 UTC · source 2022-08-29 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 E Excluded after deficient or non-compliant submission was not corrected 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 E Excluded after deficient or non-compliant submission was not corrected bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 E Excluded after deficient or non-compliant submission was not corrected 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 79644-220-01 Hand Sanitizer 50 mL in 1 BOTTLE AEROSOL, FOAM 50 1 79644-220-02 Hand Sanitizer 160 mL in 1 BOTTLE AEROSOL, FOAM 160 1 79644-220-03 Hand Sanitizer 250 mL in 1 BOTTLE AEROSOL, FOAM 250 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 79644-220 HAND SANITIZER AEROSOL, FOAM [TROKAR, S.A. DE C.V.] 1 Legacy NDC, 1 package rows 20210526_c333dda1-0f5e-8b31-e053-2995a90a2c8f.zip 79644-220 HAND SANITIZER AEROSOL, FOAM [TROKAR, S.A. DE C.V.] 1 Legacy NDC, 1 package rows 20210526_c333fa46-f87f-d26a-e053-2a95a90ae1d3.zip 79644-220 HAND SANITIZER AEROSOL, FOAM [TROKAR, S.A. DE C.V.] 1 Legacy NDC, 1 package rows 20210526_c333c252-28fe-0407-e053-2995a90ac18e.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 79644-220-01 79644022001 50 mL in 1 BOTTLE (79644-220-01) 50 ml 2020-03-30 0000-00-00 No No Current