Foamgle Foam Super Mint Mouthwash
NDC Package 50555-220-02

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

Package Information

Foamgle Foam Super Mint (allantoin) mouthwashes 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 mouthwash delivery system. Marketed by Kmpharmaceutical Co.,ltd, this product is identified by NDC 50555-220.

Identification & Billing

NDC Package Code
50555-220-02
Package Description
1 BOTTLE in 1 CARTON / 150 mL in 1 BOTTLE (50555-220-01)
Product Code
50555-220
11-Digit Billing Format
50555022002

Clinical Specifications

Proprietary Name
Foamgle Foam Super Mint
Non-Proprietary Name
Allantoin
Substance Name
Allantoin
Dosage Form
Mouthwash - An aqueous solution which is most often used for its deodorant, refreshing, or antiseptic effect.
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
02-01-2026
Listing Expiration
12-31-2027
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 50555-220-02 identifies a specific commercial package of 1 bottle in 1 carton / 150 ml in 1 bottle (50555-220-01) of Foamgle Foam Super Mint, a human over the counter drug labeled by Kmpharmaceutical Co.,ltd. This mouthwash 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 February 01, 2026. The current certification is valid through December 31, 2027.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 50555022002. 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)
50555-220-02
11-Digit CMS (5-4-2)
50555-0220-02

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