Home NDC 77263-002-01 Foaming Hand Sanitizer
Product NDC 77263-002
Requested package NDC 77263-002-01
11-digit product format 772630002
Labeler code 77263
Product ID 77263-002_d447dbbd-bb88-687a-e053-2995a90af024
Type HUMAN OTC DRUG
Nonproprietary name Benzalkonium chloride
Dosage form LIQUID
Route TOPICAL
Labeler Suzhou HVHA Medical Technology Development Co.,Ltd.
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-05-03
Marketing end 0000-00-00
Substance BENZALKONIUM CHLORIDE
Active strength 1 mg/mL
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 · 15 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…
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 77263-002-01 Foaming Hand Sanitizer 50 mL in 1 BOTTLE LIQUID 50 2 77263-002-02 Foaming Hand Sanitizer 100 mL in 1 BOTTLE LIQUID 100 2 77263-002-03 Foaming Hand Sanitizer 150 mL in 1 BOTTLE LIQUID 150 2 77263-002-04 Foaming Hand Sanitizer 200 mL in 1 BOTTLE LIQUID 200 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 77263-002 FOAMING HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [SUZHOU HVHA MEDICAL TECHNOLOGY DEVELOPMENT CO.,LTD.] 2 Legacy NDC, 4 package rows 20211230_e23cee3c-7bcc-47ac-9602-9a2ddca78c28.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 77263-002-01 77263000201 50 mL in 1 BOTTLE (77263-002-01) 50 ml 2020-05-03 0000-00-00 No No Current