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Poland· PL-100381460

Vicks Antigrip Dzień i Noc

A other cold preparations product containing paracetamolum + pseudoephedrini hydrochloridum; paracetamolum + diphenhydramini hydrochloridum, registered in Poland by WICK Pharma Zweigniederlassung der Procter & Gamble GmbH. The same ATC class is registered in 8 of our 19 countries.

ATC R05X

Checked against URPL (Poland) on

Informational only — not a medical device.

SOURCE REGISTER · PLURPL (Poland)normalisedVicks Antigrip Dzień i NocATCR05XREGISTER NO.PL-100381460PACKS LISTED1CHECKEDSeptember 27, 2026

Where it is registered

Paracetamolum + pseudoephedrini hydrochloridum; paracetamolum + diphenhydramini hydrochloridum is registered in 8 of 19 countries.

Countries holding a registration under ATC R05X (other cold preparations), each read from that country’s own register.

  • This record: Poland, from URPL (Poland)
  • 5 of them publish a price we can compare per daily dose

Paracetamolum + pseudoephedrini hydrochloridum; paracetamolum + diphenhydramini hydrochloridum · ATC R05X

8 / 19 countries

  • Belgiumprice
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Ireland
  • Netherlands
  • Polandprice
  • Switzerlandprice
Blue: a registration under this ATC code. The ringed marker is this record’s country. Markets marked price publish a price we can compare per daily dose.

The record

At a glance

URPL (Poland)
Active substance
Paracetamolum + Pseudoephedrini hydrochloridum; Paracetamolum + Diphenhydramini hydrochloridum
Manufacturer
WICK Pharma Zweigniederlassung der Procter & Gamble GmbH
Country
Poland (PL)
ATC code
R05X
ATC class
OTHER COLD PREPARATIONS
Reimbursed
Not published by this register
Source register
URPL (Poland)
Last checked
September 27, 2026

Packs & prices · 1

  • gtin
    05909991469009

Regulatory notes

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

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/eac3d60f-fa41-44c6-9cf4-16a4287111c6
GET /v1/drugs/eac3d60f-fa41-44c6-9cf4-16a4287111c6?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": "Tabletki powlekane",
  "source": "urpl",
  "strength": "500 mg + 60 mg; 500 mg + 25 mg",
  "packaging": "05909991469009 ¦ Rp ¦ 142384\n12 tabl. na dzień ¦ 4 tabl. na noc",
  "substance": "Paracetamolum 500 mg - tabletka na dzień (żółta) + Paracetamolum 500 mg - tabletka na noc (niebieska) + Pseudoephedrini hydrochloridum 60 mg - tabletka na dzień (żółta) + Diphenhydramini hydrochloridum 25 mg - tabletka na noc (niebieska)",
  "common_name": "Paracetamolum + Pseudoephedrini hydrochloridum; Paracetamolum + Diphenhydramini hydrochloridum",
  "pl_product_id": "100381460",
  "pozwolenie_nr": "28431",
  "auth_procedure": "DCP",
  "authorisation_validity": "Bezterminowe"
}

See everything about paracetamolum + pseudoephedrini hydrochloridum; paracetamolum + diphenhydramini hydrochloridum.

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.