Germany· DE-A57-968ec18ddabde6e0
Tinatox
A tolnaftate product containing tolnaftate, registered in Germany by Leyh Pharma Gmbh. The same ATC class is registered in 6 of our 19 countries.
Checked against EMA Article 57 (European Union) on
Informational only — not a medical device.
Where it is registered
Tolnaftate is registered in 6 of 19 countries.
Countries holding a registration under ATC D01AE18 (tolnaftate), each read from that country’s own register.
- This record: Germany, from EMA Article 57 (European Union)
- 2 of them publish a price we can compare per daily dose
Tolnaftate · ATC D01AE18
6 / 19 countries
- Canada
- Germany
- Japan
- Spainprice
- United Kingdom
- United Statesprice
The record
At a glance
EMA Article 57 (European Union)- Active substance
- Tolnaftate
- Manufacturer
- Leyh Pharma Gmbh
- Country
- Germany (DE)
- ATC code
- D01AE18
- ATC class
- Tolnaftate
- Defined daily dose
- 15 mg, T
- Reimbursed
- Not published by this register
- Source register
- EMA Article 57 (European Union)
- Last checked
- September 30, 2026
Packs & prices · 0
No packs listed by the register for this record.
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Tolnaftate in 4 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United StatesACTIV-CHARCOAL ANTIFUNGALHONG KONG UNORDERED TRADING CO., LIMITED
- CanadaDR. SCHOLL'S ATHLETE'S FOOT SPRAY POWDERSCHOLL'S WELLNESS COMPANY
- United KingdomDual Action Athlete's Foot 0.12% sprayThe Boots Company Plc
- SpainSOLUFUNGIN 10 mg/ml SOLUCION CUTANEAArafarma Group S.A.
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- United Kingdom (Northern Ireland) · Carnation Athlete's Foot Powder, Scholl Athlete’s Foot
- Hungary · Chinofungin, Digifungin
- Ireland · Scholl Athlete's Foot
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 EMA Article 57 (European Union). 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/989f6dc5-c4de-474f-bb7a-4cb13f3d3139 GET /v1/drugs/989f6dc5-c4de-474f-bb7a-4cb13f3d3139?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.
{
"pzn": null,
"route": "Cutaneous Use",
"source": "ema_art57_de",
"ma_number": null,
"substance": "Tolnaftate",
"atc_from_source": null,
"authorisation_country": "Germany"
}See everything about tolnaftate.
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.