Poland· PL-100098616

Mucofalk O

A drugs for constipation product containing plantaginis ovatae testa, registered in Poland by Dr. Falk Pharma GmbH.

ATC A06A

Checked against URPL (Poland) on

Informational only — not a medical device.

SOURCE REGISTER · PLURPL (Poland)normalisedMucofalk OATCA06AREGISTER NO.PL-100098616PACKS LISTED2CHECKEDAugust 9, 2026

The record

At a glance

URPL (Poland)
Active substance
Plantaginis ovatae testa
Manufacturer
Dr. Falk Pharma GmbH
Country
Poland (PL)
ATC code
A06A
ATC class
DRUGS FOR CONSTIPATION
Reimbursed
Not published by this register
Source register
URPL (Poland)
Last checked
August 9, 2026

Packs & prices · 2

  • gtin
    05909990844517
  • gtin
    05909990844524

Regulatory notes

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

Same medicine, other countries

Plantaginis ovatae testa in 7 other countries

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

All plantaginis ovatae testa products

Authorised across Europe · EMA

The same active substance is authorised in 17 EEA countries. Names it is sold under:

  • Belgium · Colofiber, Spagulax Brause
  • Bulgaria · Мукофалк Портокал
  • Cyprus · Mucofalk Orange
  • Germany · Agiocur, Flosine Balance
  • Denmark · Husk Psyllium-Frøskaller
  • Spain · Cenat, Plantaben
  • Finland · Agiocur, Vi-Siblin
  • France · Psylia, Spagulax
  • United Kingdom (Northern Ireland) · Ispagel Orange, Ispaghula Husk Tillomed Laboratories Limited
  • Lithuania · Mucofalk Apelsinų
  • Luxembourg · Agiocur, Psylia
  • Latvia · Mucofalk Orange
  • Netherlands · Metamucil Suikervrij Lemon, Metamucil Suikervrij Orange
  • Norway · Vi-Siblin
  • Portugal · Mucofalk
  • Sweden · Vi-Siblin, Vi-Siblin S
  • Slovenia · Mucofalk Z Okusom Pomaranče

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/dd03e4e6-6519-47b5-8564-3bdc0b5ec0d8
GET /v1/drugs/dd03e4e6-6519-47b5-8564-3bdc0b5ec0d8?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": "Granulat do sporządzania zawiesiny doustnej",
  "source": "urpl",
  "strength": "-",
  "packaging": "05909990844517 ¦ OTC ¦ 16844\n20 sasz. 5 g\n05909990844524 ¦ OTC ¦ Skasowane ¦ 16845\n1 op. 150 g",
  "substance": "Plantaginis ovatae semins tegumentum 3.25 g",
  "common_name": "Plantaginis ovatae testa",
  "pl_product_id": "100098616",
  "pozwolenie_nr": "08445",
  "auth_procedure": "NAR",
  "authorisation_validity": "2023-08-09"
}

See everything about plantaginis ovatae testa.

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.