Home NDC 75132-013-01 Foam Hand Sanitizer
Product NDC 75132-013
Requested package NDC 75132-013-01
11-digit product format 751320013
Labeler code 75132
Product ID 75132-013_afa78045-94dc-0360-e053-2995a90a6cca
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 75132-013-01 Foam Hand Sanitizer 236 mL in 1 BOTTLE LIQUID 236 1 75132-013-02 Foam Hand Sanitizer 300 mL in 1 BOTTLE LIQUID 300 1 75132-013-03 Foam Hand Sanitizer 450 mL in 1 BOTTLE LIQUID 450 1 75132-013-04 Foam Hand Sanitizer 500 mL in 1 BOTTLE LIQUID 500 1 75132-013-05 Foam Hand Sanitizer 1000 mL in 1 BOTTLE LIQUID 1000 1 75132-013-06 Foam Hand Sanitizer 3785 mL in 1 BOTTLE LIQUID 3785 1 75132-013-07 Foam Hand Sanitizer 5000 mL in 1 BOTTLE LIQUID 5000 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 75132-013 FOAM HAND SANITIZER LIQUID [GUANGDONG KEMEI PHARMACEUTICAL TECHNOLOGY CO., LTD.] 1 Legacy NDC, 7 package rows 20200920_afa783c4-405d-cd70-e053-2a95a90ac94c.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 75132-013-01 75132001301 236 mL in 1 BOTTLE (75132-013-01) 236 ml 2020-04-12 0000-00-00 No No Current