Home NDC 74895-102-04 Hand Sanitizer
Product NDC 74895-102
Requested package NDC 74895-102-04
11-digit product format 748950102
Labeler code 74895
Product ID 74895-102_b8a3181d-9901-454f-e053-2995a90a96c0
Type HUMAN OTC DRUG
Nonproprietary name ALCOHOL
Dosage form LIQUID
Route TOPICAL
Labeler GUANGDONG HAOSHUN ODIS TECHNOLOGY COMPANY LIMITED
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-04-08
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 74895-102-02 Hand Sanitizer 180 mL in 1 BOTTLE, PUMP LIQUID 180 4 74895-102-03 Hand Sanitizer 450 mL in 1 BOTTLE, SPRAY LIQUID 450 4 74895-102-04 Hand Sanitizer 500 mL in 1 BOTTLE, SPRAY LIQUID 500 4 74895-102-05 Hand Sanitizer 650 mL in 1 BOTTLE, SPRAY LIQUID 650 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 74895-102 HAND SANITIZER (ALCOHOL) LIQUID [GUANGDONG HAOSHUN ODIS TECHNOLOGY COMPANY LIMITED] 4 Legacy NDC, 4 package rows 20210112_a2cabf40-150e-5ddf-e053-2995a90a7406.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 74895-102-04 74895010204 500 mL in 1 BOTTLE, SPRAY (74895-102-04) 500 ml 2020-04-08 0000-00-00 No No Current