Home NDC 47593-521-38 Ecolab
Product NDC 47593-521
Requested package NDC 47593-521-38
11-digit product format 475930521
Labeler code 47593
Product ID 47593-521_4b51435a-39da-4b16-9497-76966b15dec6
Type HUMAN OTC DRUG
Nonproprietary name Benzalkonium chloride
Dosage form SOLUTION
Route TOPICAL
Labeler Ecolab Inc.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2014-09-15
Substance BENZALKONIUM CHLORIDE
Active strength 5.5 mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes 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 · 12 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…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Ecolab
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE 5.5 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination F5UM2KM3W7 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1549867 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 47593-521-38 Ecolab 500 mL in 1 BOTTLE, PLASTIC SOLUTION 500 5 47593-521-41 Ecolab 750 mL in 1 BOTTLE, PLASTIC SOLUTION 750 5 47593-521-56 Ecolab 1200 mL in 1 BOTTLE, PLASTIC SOLUTION 1200 5 47593-521-57 Ecolab 535 mL in 1 BOTTLE, PLASTIC SOLUTION 535 5 47593-521-59 Ecolab 1250 mL in 1 BOTTLE, PLASTIC SOLUTION 1250 5 47593-521-70 Ecolab 1200 mL in 1 BOTTLE, PLASTIC SOLUTION 1200 5
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 47593-521 ECOLAB (BENZALKONIUM CHLORIDE) SOLUTION [ECOLAB INC.] 5 Current NDC, Legacy NDC, 6 package rows 20250406_f646187a-6f78-436c-a397-7541a2c691b8.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
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 47593-521-38 47593052138 500 mL in 1 BOTTLE, PLASTIC (47593-521-38) 500 ml 2014-09-15 0000-00-00 No No Current