United States· US:0220-4821_0a33fb78-6d1d-3344-e063-6394a90a1861
Sulphur
A sulfur product containing sulfur, registered in United States by Boiron. The same ATC class is registered in 5 of our 19 countries.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
Where it is registered
Sulfur is registered in 5 of 19 countries.
Countries holding a registration under ATC D10AB02 (sulfur), each read from that country’s own register.
- This record: United States, from FDA National Drug Code directory (United States)
- 3 of them publish a price we can compare per daily dose
Sulfur · ATC D10AB02
5 / 19 countries
- Finlandprice
- Japan
- Spainprice
- United Kingdom
- United Statesprice
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- SULFUR
- Manufacturer
- Boiron
- Country
- United States (US)
- ATC code
- D10AB02
- ATC class
- Sulfur
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- September 27, 2026
Packs & prices · 2
- ndc11022048214110 [hp_M] in 1 TUBE (0220-4821-41)
- ndc110220-4821-41
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Sulfur in 5 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- BelgiumLuffeelHeel Belgium
- United KingdomSCC scalp ointmentSpecial Order
- FinlandSULFUR
- IrelandSULFURA. Nelson & Company Limited
- Japanイオウ
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- France · Soufre Granions
- Hungary · Detergens Sulfuratum Fono Vii, Detergens Sulfuratum Fono Viii.
- Latvia · Sera Rff
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/c4fcca03-8070-4db7-ad10-be2d63b22f3e GET /v1/drugs/c4fcca03-8070-4db7-ad10-be2d63b22f3e?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": "10",
"substance": "SULFUR",
"productndc": "0220-4821",
"dosage_form": "PELLET",
"dea_schedule": null,
"strength_unit": "[hp_M]/10[hp_M]",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC"
}See everything about sulfur.
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.