Ireland· IE-PA-PA1113/025/002
Dioralyte Citrus Powder for Oral Solution
A oral rehydration salt formulations product containing glucose + sodium chloride + disodium hydrogen citrate + potassium chloride, registered in Ireland by Phoenix Labs. The same ATC class is registered in 5 of our 19 countries.
Checked against HPRA (Ireland) on
Informational only — not a medical device.
Where it is registered
Glucose + sodium chloride + disodium hydrogen citrate + potassium chloride is registered in 5 of 19 countries.
Countries holding a registration under ATC A07CA (oral rehydration salt formulations), each read from that country’s own register.
- This record: Ireland, from HPRA (Ireland)
- 4 of them publish a price we can compare per daily dose
Glucose + sodium chloride + disodium hydrogen citrate + potassium chloride · ATC A07CA
5 / 19 countries
- Finlandprice
- Ireland
- Norwayprice
- Polandprice
- Switzerlandprice
The record
At a glance
HPRA (Ireland)- Active substance
- Glucose + Sodium chloride + Disodium hydrogen citrate + Potassium chloride
- Manufacturer
- Phoenix Labs
- Country
- Ireland (IE)
- ATC code
- A07CA
- ATC class
- Oral rehydration salt formulations
- Reimbursed
- Not published by this register
- Source register
- HPRA (Ireland)
- Last checked
- September 28, 2026
Packs & prices · 1
- ie_pa_numberPA1113/025/002
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Glucose + sodium chloride + disodium hydrogen citrate + potassium chloride in 1 other country
What each register calls a product with the same active substance — salts and hydrates count as the same.
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Germany · Oralpädon, Oralpädon Erdbeere
- United Kingdom (Northern Ireland) · Dioralyte Blackcurrant, Dioralyte Citrus
- Portugal · Dioralyte
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/c420ce8f-5c00-4c7f-adba-075f7589aed7 GET /v1/drugs/c420ce8f-5c00-4c7f-adba-075f7589aed7?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": "Powder for oral solution",
"routes": [
"Oral use"
],
"source": "hpra",
"atc_all": [
"A07CA"
],
"strength": null,
"pa_number": "PA1113/025/002",
"substances": [
"Glucose",
"Sodium chloride",
"Disodium hydrogen citrate",
"Potassium chloride"
],
"legal_basis": "Full application (Article 8(3) of Directive No 2001/83/EC)",
"market_info": "Marketed",
"authorised_at": "03/06/1992",
"dispensing_status": "Product not subject to medical prescription",
"registration_status": "AU",
"supply_legal_status": "Supply through pharmacies only",
"interchangeable_code": null
}See everything about glucose + sodium chloride + disodium hydrogen citrate + potassium chloride.
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.