What is NDC 50555-210?

50555-210 is the product NDC for Foamgle Foam Mouthwash Super Mint, Allantoin .05 g/100mL liquid, listed with the FDA by KMPHARMACEUTICAL CO.,LTD. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Foamgle Foam Mouthwash Super Mint (Allantoin).

KMPHARMACEUTICAL CO.,LTD, NDC labeler code 50555. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Foamgle Foam Mouthwash Super Mint?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Foamgle Foam Mouthwash Super Mint NDC 50555-210

NDC codes

FDA NDC Directory

Product NDC (as listed)50555-210Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50555-0210Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
50555-210-02	5055502100250555021002	1 BOTTLE in 1 CARTON (50555-210-02) / 50 mL in 1 BOTTLE (50555-210-01)Marketed from May 1, 2025

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Foamgle Foam Mouthwash Super Mint
Generic name (nonproprietary): allantoin
Active ingredients: Allantoin — .05 g/100mL
Dosage form: Liquid
Route: Oral
Labeler: KMPHARMACEUTICAL CO.,LTDNDC labeler code 50555
Product type: Over-the-counter drug
Marketing category: Unapproved drug (other)
Marketing start: May 1, 2025
Listing expires: Dec 31, 2026
Identifiers: Product ID 50555-210_352342bf-e2de-3a2c-e063-6294a90a200eSPL ID 352342bf-e2de-3a2c-e063-6294a90a200eSPL set ID 352342bf-e2dd-3a2c-e063-6294a90a200eUNII 344S277G0Z

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N450555021002 followed by a unit qualifier and the quantity

Package 50555-0210-02. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective May 14, 2025.

Indications (excerpt from the label)

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

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 50555-210

What is NDC 50555-210?: 50555-210 is the product NDC for Foamgle Foam Mouthwash Super Mint, Allantoin .05 g/100mL liquid, listed with the FDA by KMPHARMACEUTICAL CO.,LTD. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Foamgle Foam Mouthwash Super Mint (Allantoin).
What is the active ingredient?: Allantoin.
Who is the labeler?: KMPHARMACEUTICAL CO.,LTD, NDC labeler code 50555. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Foamgle Foam Mouthwash Super Mint?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Foamgle Foam Mouthwash Super Mint (Allantoin) NDC 50555-210