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Ireland· IE-PA-PA23259/018/001

Minims Povidone Iodine 5% w/v Eye Drops, Solution

A povidone-iodine product containing iodinated povidone, registered in Ireland by Bausch + Lomb Ireland Limited. The same ATC class is registered in 11 of our 19 countries.

ATC S01AX18

Checked against HPRA (Ireland) on

Informational only — not a medical device.

SOURCE REGISTER · IEHPRA (Ireland)normalisedMinims Povidone Iodine 5% w/v Eye Dro…ATCS01AX18REGISTER NO.IE-PA-PA23259/018/001PACKS LISTED1CHECKEDSeptember 28, 2026

Where it is registered

Povidone-iodine is registered in 11 of 19 countries.

Countries holding a registration under ATC S01AX18 (povidone-iodine), each read from that country’s own register.

  • This record: Ireland, from HPRA (Ireland)
  • 7 of them publish a price we can compare per daily dose

Povidone-iodine · ATC S01AX18

11 / 19 countries

  • Belgiumprice
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • Ireland
  • Netherlands
  • Norwayprice
  • Polandprice
  • United Kingdom
  • United Statesprice
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

HPRA (Ireland)
Active substance
Iodinated povidone
Manufacturer
Bausch + Lomb Ireland Limited
Country
Ireland (IE)
ATC code
S01AX18
ATC class
Povidone-iodine
Reimbursed
Not published by this register
Source register
HPRA (Ireland)
Last checked
September 28, 2026

Packs & prices · 1

  • ie_pa_number
    PA23259/018/001

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 HPRA (Ireland). 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/ed800881-6c52-47ef-bc3a-1e9a9dd07d39
GET /v1/drugs/ed800881-6c52-47ef-bc3a-1e9a9dd07d39?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": "Eye drops, solution",
  "routes": [
    "Ocular use"
  ],
  "source": "hpra",
  "atc_all": [
    "S01AX",
    "S01AX18"
  ],
  "strength": null,
  "pa_number": "PA23259/018/001",
  "substances": [
    "Iodinated povidone"
  ],
  "legal_basis": "Hybrid application (Article 10(3) of Directive No 2001/83/EC)",
  "market_info": "Marketed",
  "authorised_at": "14/12/2012",
  "dispensing_status": "Product subject to prescription which may not be renewed (A)",
  "registration_status": "AU",
  "supply_legal_status": "Supply through pharmacies only",
  "interchangeable_code": null
}

See everything about povidone-iodine.

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.