Home NDC 0404-6735-01 BZK
Product NDC 0404-6735
Requested package NDC 0404-6735-01
11-digit product format 004046735
Labeler code 0404
Product ID 0404-6735_1522e337-1394-24fa-e063-6394a90ae000
Type HUMAN OTC DRUG
Nonproprietary name benzalkonium chloride
Dosage form LIQUID
Route TOPICAL
Labeler Henry Schein Inc.
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2013-01-07
Substance BENZALKONIUM CHLORIDE
Active strength .0013 g/g
NDC exclude flag No
Listing certified through 2027-12-31
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 · 6 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 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…2021-12-27 23:28 UTC · source 2021-12-27 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 9bebd1f3094a…5416666fcb17…
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 BZK
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE .0013 g/g
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 SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0404-6735-01 BZK 2.5 g in 1 PACKET LIQUID 2.5 5 0404-6735-01 BZK 100 in 1 BOX LIQUID 100 5
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0404-6735 BZK (BENZALKONIUM CHLORIDE) LIQUID [HENRY SCHEIN INC.] 5 Current NDC, Legacy NDC, 2 package rows 20240404_ff877b63-fa58-4770-a882-694eda33203b.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 99 of 114 · 2,275 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 0404-6735-01 00404673501 100 PACKET in 1 BOX (0404-6735-01) / 2.5 g in 1 PACKET 100 packet 2016-12-01 No No Current