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United States· US:50555-220_4c006ee3-bf6a-e65c-e063-6294a90a4b96

Foamgle Foam Super Mint

A medicinal product containing allantoin, registered in United States by KMPHARMACEUTICAL CO.,LTD.

US label

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedFoamgle Foam Super MintATC—REGISTER NO.US:50555-220_4c006ee3…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
ALLANTOIN
Manufacturer
KMPHARMACEUTICAL CO.,LTD
Country
United States (US)
ATC code
—
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
September 27, 2026

Packs & prices · 2

  • ndc11
    5055522002
    1 BOTTLE in 1 CARTON (50555-220-02) / 150 mL in 1 BOTTLE (50555-220-01)
  • ndc11
    50555-220-02

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same medicine, other countries

Allantoin in 1 other country

What each register calls a product with the same active substance — salts and hydrates count as the same.

All allantoin products

Authorised across Europe · EMA

The same active substance is authorised in 1 EEA country. Names it is sold under:

  • Poland · Alantan

Source: European Medicines Agency, Article 57 product data.

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.

For developers

The same record over the API, and the raw payload
GET /v1/drugs/eb21c9fb-c8c2-4801-84ac-d01f46a94c3b
GET /v1/drugs/eb21c9fb-c8c2-4801-84ac-d01f46a94c3b?format=fhir

Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.

{
  "route": "ORAL",
  "source": "ndc",
  "strength": ".05",
  "substance": "ALLANTOIN",
  "productndc": "50555-220",
  "dosage_form": "MOUTHWASH",
  "dea_schedule": null,
  "strength_unit": "g/100mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED DRUG OTHER"
}

See everything about allantoin.

This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.