Home NDC 74895-101-05 Hand Sanitizer
Product NDC 74895-101
Requested package NDC 74895-101-05
11-digit product format 748950101
Labeler code 74895
Product ID 74895-101_b8a3dfe6-643a-a98c-e053-2a95a90a21ed
Type HUMAN OTC DRUG
Nonproprietary name ALCOHOL
Dosage form GEL
Route TOPICAL
Labeler GUANGDONG HAOSHUN ODIS TECHNOLOGY COMPANY LIMITED
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-04-07
Marketing end 0000-00-00
Substance ALCOHOL
Active strength 80 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 · 16 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…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 74895-101-01 Hand Sanitizer 80 mL in 1 TUBE GEL 80 6 74895-101-02 Hand Sanitizer 480 mL in 1 BOTTLE, PUMP GEL 480 6 74895-101-03 Hand Sanitizer 290 mL in 1 BOTTLE, PUMP GEL 290 6 74895-101-04 Hand Sanitizer 236 mL in 1 BOTTLE, PUMP GEL 236 6 74895-101-05 Hand Sanitizer 60 mL in 1 BOTTLE, PUMP GEL 60 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 74895-101 HAND SANITIZER (ALCOHOL) GEL [GUANGDONG HAOSHUN ODIS TECHNOLOGY COMPANY LIMITED] 6 Legacy NDC, 5 package rows 20210112_a2baa7aa-5878-6173-e053-2995a90a2e74.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 74895-101-05 74895010105 60 mL in 1 BOTTLE, PUMP (74895-101-05) 60 ml 2020-05-24 0000-00-00 No No Current