Benzethonium Chloride Plus Dyclonine Hydrochloride Liquid
NDC Package 72446-100-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Benzethonium Chloride Plus Dyclonine Hydrochloride (liquid bandage) liquids is for adults and children 2 years of age and olderclean affected areaapply a small amount on the area 1 to 3 times daily and let drya second coating may be applied for extra protectionchildren under 2 years of age: consult a doctor. This formulation utilizes a liquid delivery system. Marketed by Hudson Health Llc, this product is identified by NDC 72446-100 and is authorized under FDA application M003.

Identification & Billing

NDC Package Code
72446-100-01
Package Description
1 BOTTLE, WITH APPLICATOR in 1 CARTON / 29.6 mL in 1 BOTTLE, WITH APPLICATOR
Product Code
72446-100
11-Digit Billing Format
72446010001
RxNorm Crosswalk
  • RxCUI: 1048366 - benzethonium Cl 0.2 % / dyclonine HCl 0.75 % Topical Solution
  • RxCUI: 1048366 - benzethonium chloride 2 MG/ML / dyclonine hydrochloride 7.5 MG/ML Topical Solution

Clinical Specifications

Proprietary Name
Benzethonium Chloride Plus Dyclonine Hydrochloride
Non-Proprietary Name
Liquid Bandage
Substance Name
Benzethonium Chloride; Dyclonine Hydrochloride
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s)
Usage Information
For adults and children 2 years of age and olderclean affected areaapply a small amount on the area 1 to 3 times daily and let drya second coating may be applied for extra protectionchildren under 2 years of age: consult a doctor

Regulatory & Marketing

Labeler Name
Hudson Health Llc
Product Type
Human Otc Drug
FDA Application #
M003
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-01-2018
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 72446-100-01 identifies a specific commercial package of 1 bottle, with applicator in 1 carton / 29.6 ml in 1 bottle, with applicator of Benzethonium Chloride Plus Dyclonine Hydrochloride, a human over the counter drug labeled by Hudson Health Llc. This liquid is formulated for topical use and contains benzethonium chloride; dyclonine hydrochloride as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Hudson Health Llc on September 01, 2018. The current certification is valid through December 31, 2026.

How is this Hudson Health Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72446010001. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
72446-100-01
11-Digit CMS (5-4-2)
72446-0100-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.