Home NDC 76735-001-03 Happ Hand Sanitizer
Product NDC 76735-001
Requested package NDC 76735-001-03
11-digit product format 767350001
Labeler code 76735
Product ID 76735-001_865d093f-87db-46b5-aecf-6b2d5b5244a7
Type HUMAN OTC DRUG
Nonproprietary name Alcohol
Dosage form GEL
Route TOPICAL
Labeler Fujian Happiness Biotech Technology Co., Ltd.
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-04-26
Marketing end 0000-00-00
Substance ALCOHOL
Active strength 65 mL/100mL
NDC exclude flag No
Listing certified through 2021-12-31
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 · 18 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…2022-04-09 23:13 UTC · source 2022-04-08 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 bd6a592717d7…303034d00443…
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 76735-001-01 Happ Hand Sanitizer 50 mL in 1 BOTTLE, PLASTIC GEL 50 1 76735-001-02 Happ Hand Sanitizer 100 mL in 1 BOTTLE, PLASTIC GEL 100 1 76735-001-03 Happ Hand Sanitizer 236 mL in 1 BOTTLE, PLASTIC GEL 236 1 76735-001-04 Happ Hand Sanitizer 500 mL in 1 BOTTLE, PLASTIC GEL 500 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 76735-001 HAPP HAND SANITIZER (ALCOHOL) GEL [FUJIAN HAPPINESS BIOTECH TECHNOLOGY CO., LTD.] 1 Legacy NDC, 4 package rows 20200715_99611b02-b058-4c07-8800-5b76bc854850.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 76735-001-03 76735000103 236 mL in 1 BOTTLE, PLASTIC (76735-001-03) 236 ml 2020-04-26 0000-00-00 No No Current