Foamgle Foam Mouthwash Super Mint Liquid
NDC Package 50555-210-02

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

Package Information

Foamgle Foam Mouthwash Super Mint (allantoin) liquids is use(s)■ Aids in the prevention of dental cavities.■ Helps remove plaque that leads to gingivitis, an early form of gum disease.■ Helps protect the mouth against everyday irritants■ Freshens breath while protecting oral tissues■ Helps soothe and protect irritated gums and mouth. This formulation utilizes a liquid delivery system. Marketed by Kmpharmaceutical Co.,ltd, this product is identified by NDC 50555-210.

Identification & Billing

NDC Package Code
50555-210-02
Package Description
1 BOTTLE in 1 CARTON / 50 mL in 1 BOTTLE (50555-210-01)
Product Code
50555-210
11-Digit Billing Format
50555021002

Clinical Specifications

Proprietary Name
Foamgle Foam Mouthwash Super Mint
Non-Proprietary Name
Allantoin
Substance Name
Allantoin
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
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
ALLANTOIN .05 g/100mL
Usage Information
Use(s)■ Aids in the prevention of dental cavities.■ Helps remove plaque that leads to gingivitis, an early form of gum disease.■ Helps protect the mouth against everyday irritants■ Freshens breath while protecting oral tissues■ Helps soothe and protect irritated gums and mouth

Regulatory & Marketing

Labeler Name
Kmpharmaceutical Co.,ltd
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
05-01-2025
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 50555-210-02 identifies a specific commercial package of 1 bottle in 1 carton / 50 ml in 1 bottle (50555-210-01) of Foamgle Foam Mouthwash Super Mint, a human over the counter drug labeled by Kmpharmaceutical Co.,ltd. This liquid is formulated for oral use and contains allantoin 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 Kmpharmaceutical Co.,ltd on May 01, 2025. The current certification is valid through December 31, 2026.

How is this Kmpharmaceutical Co.,ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 50555021002. 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)
50555-210-02
11-Digit CMS (5-4-2)
50555-0210-02

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