Home NDC 69771-062-01 BZK CLEANSER
Product NDC 69771-062
Requested package NDC 69771-062-01
11-digit product format 697710062
Labeler code 69771
Product ID 69771-062_415eb5fb-5f89-d2dd-e063-6394a90abe5d
Type HUMAN OTC DRUG
Nonproprietary name BENZALKONIUM CHLORIDE
Dosage form SOLUTION
Route TOPICAL
Labeler Geri-Gentle Corporation
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-10-17
Substance BENZALKONIUM CHLORIDE
Active strength .1 g/100g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes 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 CLEANSER
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE .1 g/100g
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.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69771-062-01 BZK CLEANSER 237 g in 1 BOTTLE, PLASTIC SOLUTION 237 1
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 9 of 115 · 2,286 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 69771-062-01 69771006201 237 g in 1 BOTTLE, PLASTIC (69771-062-01) 237 g 2025-10-17 No No Current