Home NDC 47593-670 Kay Foaming Hand Sanitizer
Product NDC 47593-670
11-digit product format 475930670
Labeler code 47593
Product ID 47593-670_b2264c8c-11ca-4017-aa68-83a06714ea93
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 2025-12-17
Substance BENZALKONIUM CHLORIDE
Active strength 1 mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Kay Foaming Hand Sanitizer
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE 1 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 1038799 Internal RxNorm 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 47593-670-59 Kay Foaming Hand Sanitizer 1250 mL in 1 BOTTLE, PLASTIC SOLUTION 1250 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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 47593-670-59 47593067059 1250 mL in 1 BOTTLE, PLASTIC (47593-670-59) 1250 ml 2025-12-17 No No Current