United States· US:87870-006_58a9ea72-2dc8-3097-e063-6394a90a477c
Natural Vine Fungal Nail Green Patches
A tolnaftate product containing tolnaftate, registered in United States by GETHSEMANE BRANCH CORPORATION. The same ATC class is registered in 6 of our 19 countries.
Checked against FDA National Drug Code directory (United States) 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: United States, from FDA National Drug Code directory (United States)
- 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
FDA National Drug Code directory (United States)- Active substance
- TOLNAFTATE
- Manufacturer
- GETHSEMANE BRANCH CORPORATION
- Country
- United States (US)
- ATC code
- D01AE18
- ATC class
- Tolnaftate
- Defined daily dose
- 15 mg, T
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- September 27, 2026
Packs & prices · 1
- ndc1187870-006-01
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.
- CanadaDR. SCHOLL'S ATHLETE'S FOOT SPRAY POWDERSCHOLL'S WELLNESS COMPANY
- United KingdomDual Action Athlete's Foot 0.12% sprayThe Boots Company Plc
- GermanyTinatoxLeyh Pharma Gmbh
- SpainSOLUFUNGIN 10 mg/ml SOLUCION CUTANEAArafarma Group S.A.
Authorised across Europe · EMA
The same active substance is authorised in 4 EEA countries. Names it is sold under:
- Germany · Tinatox
- 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 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/af89075c-a19b-466d-a564-92d18f2b883f GET /v1/drugs/af89075c-a19b-466d-a564-92d18f2b883f?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": "TOPICAL",
"source": "ndc",
"strength": "1",
"substance": "TOLNAFTATE",
"productndc": "87870-006",
"dosage_form": "PATCH",
"dea_schedule": null,
"strength_unit": "mg/1001",
"application_number": "M005",
"marketing_category": "OTC MONOGRAPH DRUG"
}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.