Home NDC 81309-005-04 Hand Sanitizer
Product NDC 81309-005
Requested package NDC 81309-005-04
11-digit product format 813090005
Labeler code 81309
Product ID 81309-005_bbbe7c97-60af-8f84-e053-2995a90a05c8
Type HUMAN OTC DRUG
Nonproprietary name Ethyl Alcohol
Dosage form GEL
Route TOPICAL
Labeler LYW BIOTECH CO LIMITED GUANGZHOU
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2021-02-01
Marketing end 0000-00-00
Substance ALCOHOL
Active strength 70 mL/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 · 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 81309-005-01 Hand Sanitizer 30 mL in 1 BOTTLE, PLASTIC GEL 30 1 81309-005-02 Hand Sanitizer 60 mL in 1 BOTTLE, PLASTIC GEL 60 1 81309-005-03 Hand Sanitizer 100 mL in 1 BOTTLE, PLASTIC GEL 100 1 81309-005-04 Hand Sanitizer 120 mL in 1 BOTTLE, PLASTIC GEL 120 1 81309-005-05 Hand Sanitizer 250 mL in 1 BOTTLE, PLASTIC GEL 250 1 81309-005-06 Hand Sanitizer 500 mL in 1 BOTTLE, PLASTIC GEL 500 1 81309-005-07 Hand Sanitizer 1000 mL in 1 BOTTLE, PLASTIC GEL 1000 1 81309-005-08 Hand Sanitizer 1500 mL in 1 BOTTLE, PLASTIC GEL 1500 1 81309-005-09 Hand Sanitizer 2000 mL in 1 BOTTLE, PLASTIC GEL 2000 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81309-005 HAND SANITIZER (ETHYL ALCOHOL) GEL [LYW BIOTECH CO LIMITED GUANGZHOU] 1 Legacy NDC, 9 package rows 20210222_bbbe7c97-60ae-8f84-e053-2995a90a05c8.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 81309-005-04 81309000504 120 mL in 1 BOTTLE, PLASTIC (81309-005-04) 120 ml 2021-02-01 0000-00-00 No No Current