Home NDC 69396-186-01 Benzalkonium Chloride
Product NDC 69396-186
Requested package NDC 69396-186-01
11-digit product format 693960186
Labeler code 69396
Product ID 69396-186_59811e83-b0cb-56d9-e063-6394a90a0653
Type HUMAN OTC DRUG
Nonproprietary name Benzalkonium Chloride Towelettes
Dosage form CLOTH
Route TOPICAL
Labeler Trifecta Pharmaceuticals USA LLC
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-05-18
Substance BENZALKONIUM CHLORIDE
Active strength .13 g/1
NDC exclude flag No
Listing certified through 2027-12-31
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 Benzalkonium Chloride
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE .13 g/1
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 1038558 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 70 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 69396-186-01 69396018601 100 PACKET in 1 BOX (69396-186-01) / 1 CLOTH in 1 PACKET 100 packet 2026-08-11 No No Current