Home NDC 50353-105-10 Purmist
Product NDC 50353-105
Requested package NDC 50353-105-10
11-digit product format 503530105
Labeler code 50353
Product ID 50353-105_e0546876-966a-a2de-e053-2995a90ad17b
Type HUMAN OTC DRUG
Nonproprietary name Benzalkonium Cl
Dosage form LIQUID
Route TOPICAL
Labeler MKR International Inc
Application part333E
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2021-04-26
Marketing end 0000-00-00
Substance BENZALKONIUM CHLORIDE
Active strength 0 g/mL
NDC exclude flag No
Listing certified through 2023-12-31
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 · 15 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…
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 50353-105-50 Purmist 60 mL in 1 BOTTLE, SPRAY LIQUID 60 7 50353-105-10 Purmist 1 in 1 BLISTER PACK LIQUID 1 3 50353-105-10 Purmist 7.1 mL in 1 BOTTLE, PUMP LIQUID 7.1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50353-105 PURMIST (BENZALKONIUM CL) LIQUID [MKR INTERNATIONAL INC] 7 Legacy NDC, 1 package rows 20220601_dbd86ed2-3bcc-67cd-e053-2995a90a9697.zip 50353-105 PURMIST (BENZALKONIUM CL) LIQUID [MKR INTERNATIONAL INC] 3 Legacy NDC, 2 package rows 20210212_958923fc-3ff8-1b38-e053-2a95a90a93ed.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 50353-105-10 50353010510 1 BOTTLE, PUMP in 1 BLISTER PACK (50353-105-10) > 7.1 mL in 1 BOTTLE, PUMP 2019-06-14 0000-00-00 No No Current