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France· FR:69544933

CYTEAL, solution moussante

A medicinal product containing chlorocrésol + diisétionate d'hexamidine + solution de digluconate de chlorhexidine, registered in France by PIERRE FABRE MEDICAMENT, on the national reimbursement list.

Reimbursed in France (Assurance maladie)

Checked against Base de données publique des médicaments — BDPM (France) on

Informational only — not a medical device.

SOURCE REGISTER · FRBase de données publique des médicament…normalisedCYTEAL, solution moussanteATC—REGISTER NO.FR:69544933PACKS LISTED2CHECKEDSeptember 12, 2026

The record

At a glance

Base de données publique des médicaments — BDPM (France)
Active substance
CHLOROCRÉSOL + DIISÉTIONATE D'HEXAMIDINE + SOLUTION DE DIGLUCONATE DE CHLORHEXIDINE
Manufacturer
PIERRE FABRE MEDICAMENT
Country
France (FR)
ATC code
—
Reimbursed
Yes
Source register
Base de données publique des médicaments — BDPM (France)
Last checked
September 12, 2026

Packs & prices · 2

1 priced
  • cip13
    3400932023592
    1 flacon(s) polyéthylène haute densité (PEHD) de 500 ml
  • cip13
    3400932046546
    1 flacon(s) polyéthylène haute densité (PEHD) de 250 ml
    EUR 2.65

Regulatory notes

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

Same medicine, other countries

Chlorocrésol + diisétionate d'hexamidine + solution de digluconate de chlorhexidine in 1 other country

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

All chlorocrésol + diisétionate d'hexamidine + solution de digluconate de chlorhexidine products

Authorised across Europe · EMA

The same active substance is authorised in 3 EEA countries. Names it is sold under:

  • Czechia · Cyteal
  • Luxembourg · Cyteal
  • Portugal · Cyteal

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 Base de données publique des médicaments — BDPM (France). 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/89690f88-e38a-44c4-8b7f-a4c1298be529
GET /v1/drugs/89690f88-e38a-44c4-8b7f-a4c1298be529?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.

{
  "cis": "69544933",
  "date_amm": "1996-08-05",
  "type_amm": "Procédure nationale",
  "numero_ue": null,
  "substance": "CHLOROCRÉSOL + DIISÉTIONATE D'HEXAMIDINE + SOLUTION DE DIGLUCONATE DE CHLORHEXIDINE",
  "statut_amm": "Autorisation active",
  "statut_bdm": null,
  "forme_pharmaceutique": "solution moussant(e)",
  "voies_administration": "cutanée",
  "etat_commercialisation": "Commercialisée",
  "surveillance_renforcee": "Non"
}

See everything about chlorocrésol + diisétionate d'hexamidine + solution de digluconate de chlorhexidine.

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.