Home NDC 11344-224-45 Foaming Hand
Product NDC 11344-224
Requested package NDC 11344-224-45
11-digit product format 113440224
Labeler code 11344
Product ID 11344-224_4cd559bd-73d9-fdfb-e063-6294a90a0afe
Type HUMAN OTC DRUG
Nonproprietary name Benzalkonium Chloride
Dosage form LOTION
Route TOPICAL
Labeler Nice-Pak Products, LLC
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-02-08
Substance BENZALKONIUM CHLORIDE
Active strength 1.3 mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Foaming Hand
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 1020365 Internal RxNorm 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 11344-224-04 Foaming Hand 750 mL in 1 BOTTLE, PLASTIC LOTION 750 18 11344-224-08 Foaming Hand 3785 mL in 1 BOTTLE, PLASTIC LOTION 3785 18 11344-224-20 Foaming Hand 44 mL in 1 BOTTLE, DISPENSING LOTION 44 18 11344-224-44 Foaming Hand 532 mL in 1 BOTTLE, PLASTIC LOTION 532 18 11344-224-45 Foaming Hand 1150 mL in 1 BOTTLE, PLASTIC LOTION 1150 18 11344-224-86 Foaming Hand 1000 mL in 1 BOTTLE, DISPENSING LOTION 1000 18 11344-224-96 Foaming Hand 222 mL in 1 BOTTLE, PUMP LOTION 222 18
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11344-224 FOAMING HAND (BENZALKONIUM CHLORIDE) LOTION [CONSUMER PRODUCT PARTNERS, LLC] 17 Current NDC, Legacy NDC, 7 package rows 20250416_2002c182-b4a6-4baa-8497-74570713b8bb.zip
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 Marketing end Sample Exclude flag Status 11344-224-45 11344022445 1150 mL in 1 BOTTLE, PLASTIC (11344-224-45) 1150 ml 2018-02-08 0000-00-00 No No Current