Home NDC 47593-692-70 EXP Foaming Hand Sanitizer
Product NDC 47593-692
Requested package NDC 47593-692-70
11-digit product format 475930692
Labeler code 47593
Product ID 47593-692_3edaece0-b4c4-46fe-bbbe-fca72128eafd
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 2025-12-30
Substance BENZALKONIUM CHLORIDE
Active strength .1 mg/100mL
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 EXP Foaming Hand Sanitizer
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE .1 mg/100mL
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 Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 47593-692-70 EXP Foaming Hand Sanitizer 1200 mL in 1 BOTTLE, PLASTIC SOLUTION 1200 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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 47593-692-70 47593069270 1200 mL in 1 BOTTLE, PLASTIC (47593-692-70) 1200 ml 2025-12-30 No No Current