Iceland· IS-IS/1/22/032/01
Ophthajod
A povidone-iodine product containing povidone, iodinated, registered in Iceland by XGX Pharma ApS. The same ATC class is registered in 11 of our 19 countries.
Checked against Icelandic Medicines Agency (Iceland) on
Informational only — not a medical device.
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: Iceland, from Icelandic Medicines Agency (Iceland)
- 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
The record
At a glance
Icelandic Medicines Agency (Iceland)- Active substance
- POVIDONE, IODINATED
- Manufacturer
- XGX Pharma ApS
- Country
- Iceland (IS)
- ATC code
- S01AX18
- ATC class
- Povidone-iodine
- Reimbursed
- Not published by this register
- Source register
- Icelandic Medicines Agency (Iceland)
- Last checked
- September 29, 2026
Packs & prices · 0
No packs listed by the register for this record.
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same class
Other records under S01AX18
Povidone-iodine, as other registers publish it.
- United StatesBetadineAlcon Laboratories, Inc.
- NorwayBetadine sterile ophtalmicAlcon Laboratories Inc
- BelgiumIso-Betadine 5 %Cooper Consumer Health
- CzechiaJODILUXOlikla s.r.o., Kostelec nad Černými Lesy
- NetherlandsMinims Povidon Jodium 5% Oogdruppels, oplossingBausch + Lomb Ireland Limited
- United KingdomMinims povidone iodine 5% eye drops 0.4ml unit doseBausch & Lomb UK Ltd
- United KingdomMinims povidone iodine 5% eye drops 0.5ml unit doseBausch & Lomb UK Ltd
- IrelandMinims Povidone Iodine 5% w/v Eye Drops, SolutionBausch + Lomb Ireland Limited
Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of Icelandic Medicines Agency (Iceland). 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/e0d73b22-31e2-4f79-818e-2e1f84f49e59 GET /v1/drugs/e0d73b22-31e2-4f79-818e-2e1f84f49e59?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": "Augndropar, lausn",
"source": "lyfjastofnun",
"atc_raw": "S01AX18",
"marketed": false,
"strength": "50 mg/ml",
"ma_number": "IS/1/22/032/01",
"substance": "POVIDONE, IODINATED",
"other_info": "Ávísun lyfsins er bundin við sérfræðinga í augnlækningum.",
"legal_status": "(R Z) Sérfræðingsmerkt (og lyfseðilsskylt)",
"ma_issued_serial": "44690"
}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.