Home NDC 54340-121 Dial Professional Antibacterial Defense Spring Water
Product NDC 54340-121
11-digit product format 543400121
Labeler code 54340
Product ID 54340-121_458696c6-881f-d85c-e063-6294a90ac119
Type HUMAN OTC DRUG
Nonproprietary name BENZALKONIUM CHLORIDE
Dosage form SOLUTION
Route TOPICAL
Labeler Henkel Corporation
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-01-01
Substance BENZALKONIUM CHLORIDE
Active strength .13 g/100mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Dial Professional Antibacterial Defense Spring Water
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE .13 g/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 RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1046593 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 54340-121-01 Dial Professional Antibacterial Defense Spring Water 3785 mL in 1 BOTTLE, DISPENSING SOLUTION 3785 2 54340-121-02 Dial Professional Antibacterial Defense Spring Water 4 in 1 CARTON SOLUTION 4 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 54340-121 DIAL PROFESSIONAL ANTIBACTERIAL DEFENSE SPRING WATER (BENZALKONIUM CHLORIDE) SOLUTION DIAL PROFESSIONAL ANTIBACTERIAL AND SENSITIVE FRAGRANCE FREE (BENZALKONIUM CHLORIDE) SOLUTION DIAL PROFESSIONAL ANTIBACTERIAL DEFENSE GOLD (BENZALKONIUM CHLORIDE) SOLUTION [HENKEL CORPORATION] 1 Current NDC, 2 package rows 20241222_29644a9d-3954-a6e5-e063-6394a90a82c7.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 Sample Exclude flag Status 54340-121-01 54340012101 3785 mL in 1 BOTTLE, DISPENSING 3785 ml Historical 54340-121-02 54340012102 4 BOTTLE, DISPENSING in 1 CARTON (54340-121-02) / 3785 mL in 1 BOTTLE, DISPENSING (54340-121-01) 2024-01-01 No No Current