Home NDC 75132-012-03 Foam Hand Sanitizer
Product NDC 75132-012
Requested package NDC 75132-012-03
11-digit product format 751320012
Labeler code 75132
Product ID 75132-012_afa7a8c4-9a04-74fe-e053-2995a90aae64
Type HUMAN OTC DRUG
Nonproprietary name Foam Hand Sanitizer
Dosage form LIQUID
Route TOPICAL
Labeler Guangdong Kemei Pharmaceutical Technology Co., Ltd.
Application part349
Marketing category OTC MONOGRAPH FINAL
Marketing start 2020-04-12
Marketing end 0000-00-00
Substance SODIUM CHLORIDE
Active strength 2 g/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.
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 75132-012-01 Foam Hand Sanitizer 3785 mL in 1 BOTTLE LIQUID 3785 2 75132-012-02 Foam Hand Sanitizer 950 mL in 1 BOTTLE LIQUID 950 2 75132-012-03 Foam Hand Sanitizer 950 mL in 1 BAG LIQUID 950 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 75132-012 FOAM HAND SANITIZER LIQUID [GUANGDONG KEMEI PHARMACEUTICAL TECHNOLOGY CO., LTD.] 2 Legacy NDC, 3 package rows 20200920_afa35c57-8ee0-cb47-e053-2995a90a1152.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 75132-012-03 75132001203 950 mL in 1 BAG (75132-012-03) 950 ml 2020-04-12 0000-00-00 No No Current