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United States· US:0220-0851_16c53262-272d-8011-e063-6294a90a4f6b

Bismuthum metallicum

A medicinal product containing bismuth, registered in United States by Boiron.

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…normalisedBismuthum metallicumATC—REGISTER NO.US:0220-0851_16c53262…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
BISMUTH
Manufacturer
Boiron
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
    0220085141
    30 [hp_C] in 1 TUBE (0220-0851-41)
  • ndc11
    0220-0851-41

Regulatory notes

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

Same medicine, other countries

Bismuth in 3 other countries

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

All bismuth products

Authorised across Europe · EMA

The same active substance is authorised in 15 EEA countries. Names it is sold under:

  • Austria · Ulcamed
  • Bulgaria · Улкамед
  • Cyprus · Bischeme, Bismuth Subcitrate Win Medica
  • Czechia · Ulcamed
  • Estonia · Ulcamed
  • Spain · Gastrodenol
  • France · Oligosol
  • Greece · Bischeme, Bismuth Krka
  • Croatia · Ulcamed
  • Hungary · Bizmut-Szubcitrát Elpen, Bizmut-Szubcitrát Win Medica
  • Lithuania · Ulcamed
  • Poland · Ulcamed
  • Romania · Ulcamed
  • Slovenia · Bizmutov Oksid Krka
  • Slovakia · Ulcamed

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/14827f34-7c62-46f0-9993-af6ac930f72c
GET /v1/drugs/14827f34-7c62-46f0-9993-af6ac930f72c?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": "30",
  "substance": "BISMUTH",
  "productndc": "0220-0851",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "strength_unit": "[hp_C]/30[hp_C]",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC"
}

See everything about bismuth.

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.