Poland· PL-100522446

Verrumal

A brak product containing acidum salicylicum + fluorouracilum, registered in Poland by Allpharm Sp. z o.o. sp.k..

ATC BRAK

Checked against URPL (Poland) on

Informational only — not a medical device.

SOURCE REGISTER · PLURPL (Poland)normalisedVerrumalATCBRAKREGISTER NO.PL-100522446PACKS LISTED1CHECKEDSeptember 27, 2026

The record

At a glance

URPL (Poland)
Active substance
Acidum salicylicum + Fluorouracilum
Manufacturer
Allpharm Sp. z o.o. sp.k.
Country
Poland (PL)
ATC code
BRAK
ATC class
BRAK
Reimbursed
Not published by this register
Source register
URPL (Poland)
Last checked
September 27, 2026

Packs & prices · 1

  • gtin
    05909991582531

Regulatory notes

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

Same medicine, other countries

Acidum salicylicum + fluorouracilum in 10 other countries

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

All acidum salicylicum + fluorouracilum products

Authorised across Europe · EMA

The same active substance is authorised in 19 EEA countries. Names it is sold under:

  • Austria · Actikerall, Verrumal
  • Czechia · Actikerall, Verrumal
  • Germany · Actikerall, Verrucutan
  • Denmark · Actikerall
  • Estonia · Actikerall
  • Spain · Actikerall, Verrucutan
  • Finland · Actikerall
  • United Kingdom (Northern Ireland) · Actikerall
  • Greece · Actiker, Verruca Hermal
  • Croatia · Verrucutan
  • Hungary · Verrumal
  • Iceland · Actikerall
  • Italy · Actikerall
  • Luxembourg · Actikerall, Verrumal
  • Latvia · Actikerall
  • Norway · Actikerall
  • Portugal · Actikerall, Verrucare
  • Sweden · Actikerall
  • Slovakia · Actikerall, Verrumal

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 URPL (Poland). 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/aa15fa50-7fb3-4b63-9087-54e309d7525d
GET /v1/drugs/aa15fa50-7fb3-4b63-9087-54e309d7525d?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.

{
  "form": "Roztwór na skórę",
  "source": "urpl",
  "strength": "100 mg/g + 5 mg/g",
  "packaging": "05909991582531 ¦ Rp ¦ 163257\n1 butelka 13 ml",
  "substance": "Acidum salicylicum 100 mg/g + Fluorouracilum 5 mg/g",
  "common_name": "Acidum salicylicum + Fluorouracilum",
  "pl_product_id": "100522446",
  "pozwolenie_nr": "261/25",
  "auth_procedure": "IR",
  "authorisation_validity": "2030-08-08"
}

See everything about acidum salicylicum + fluorouracilum.

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.