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Ireland· IE-PA-PA25506/010/001

WAXSOL 0.5% w/v Ear Drops Solution

A indifferent preparations product containing docusate sodium, registered in Ireland by Cooper Consumer Health B.V.. The same ATC class is registered in 2 of our 19 countries.

ATC S02DC

Checked against HPRA (Ireland) on

Informational only — not a medical device.

SOURCE REGISTER · IEHPRA (Ireland)normalisedWAXSOL 0.5% w/v Ear Drops SolutionATCS02DCREGISTER NO.IE-PA-PA25506/010/001PACKS LISTED1CHECKEDSeptember 28, 2026

Where it is registered

Docusate sodium is registered in 2 of 19 countries.

Countries holding a registration under ATC S02DC (indifferent preparations), each read from that country’s own register.

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

Docusate sodium · ATC S02DC

2 / 19 countries

  • Belgiumprice
  • Ireland
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
Docusate sodium
Manufacturer
Cooper Consumer Health B.V.
Country
Ireland (IE)
ATC code
S02DC
ATC class
Indifferent preparations
Reimbursed
Not published by this register
Source register
HPRA (Ireland)
Last checked
September 28, 2026

Packs & prices · 1

  • ie_pa_number
    PA25506/010/001

Regulatory notes

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

Same medicine, other countries

Docusate sodium in 6 other countries

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

All docusate sodium products

Authorised across Europe · EMA

The same active substance is authorised in 6 EEA countries. Names it is sold under:

  • Belgium · Norgalax
  • France · Jamylene, Norgalax
  • United Kingdom (Northern Ireland) · Dioctyl, Docusate Sodium Adult Typharm
  • Luxembourg · Norgalax
  • Netherlands · Norgalax
  • Poland · Laxol, Ulgix Laxi

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 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/de6fc2f3-da50-4f35-980b-82598337221c
GET /v1/drugs/de6fc2f3-da50-4f35-980b-82598337221c?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": "Ear drops, solution",
  "routes": [
    "Not Currently Available"
  ],
  "source": "hpra",
  "atc_all": [
    "S02DC"
  ],
  "strength": null,
  "pa_number": "PA25506/010/001",
  "substances": [
    "Docusate sodium"
  ],
  "legal_basis": "Full application (Article 8(3) of Directive No 2001/83/EC)",
  "market_info": "Marketed",
  "authorised_at": "03/05/2011",
  "dispensing_status": "Product not subject to medical prescription",
  "registration_status": "AU",
  "supply_legal_status": "Supply through pharmacies only",
  "interchangeable_code": null
}

See everything about docusate sodium.

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.