Home NDC 55305-144 AEROAID
Product NDC 55305-144
11-digit product format 553050144
Labeler code 55305
Product ID 55305-144_57614649-10fb-cf52-e063-6394a90a9660
Type HUMAN OTC DRUG
Nonproprietary name Benzalkonium Chloride
Dosage form SPRAY
Route TOPICAL
Labeler Aero Healthcare US LLC
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-23
Substance BENZALKONIUM CHLORIDE
Active strength 1.3 mg/mL
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 AEROAID
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE 1.3 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 1039012 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 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 55305-144-01 55305014401 59.1 mL in 1 BOTTLE (55305-144-01) 59.1 ml 2026-07-23 No No Current