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France· FR:61455112

HEXETIDINE EG LABO CONSEIL 0,1 %, solution pour bain de bouche

A medicinal product containing hexétidine, registered in France by EG LABO - LABORATOIRES EUROGENERICS.

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…normalisedHEXETIDINE EG LABO CONSEIL 0,1 %, sol…ATC—REGISTER NO.FR:61455112PACKS LISTED1CHECKEDSeptember 12, 2026

The record

At a glance

Base de données publique des médicaments — BDPM (France)
Active substance
HEXÉTIDINE
Manufacturer
EG LABO - LABORATOIRES EUROGENERICS
Country
France (FR)
ATC code
—
Reimbursed
No
Source register
Base de données publique des médicaments — BDPM (France)
Last checked
September 12, 2026

Packs & prices · 1

  • cip13
    3400922252988
    1 flacon(s) polytéréphtalate (PET) de 200 ml avec gobelet(s) doseur(s) polypropylène

Regulatory notes

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

Same medicine, other countries

Hexétidine in 7 other countries

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

All hexétidine products

Authorised across Europe · EMA

The same active substance is authorised in 17 EEA countries. Names it is sold under:

  • Austria · Hexoral
  • Belgium · Hextril
  • Cyprus · Hexalen
  • Czechia · Stopangin
  • Germany · Hexoral, Vagi-Hex
  • Estonia · Hexoral
  • United Kingdom (Northern Ireland) · Oraldene, Oraldene Icemint
  • Greece · Hexalen
  • Croatia · Belosept, Hexoral
  • Ireland · Oraldene, Oraldene Icemint
  • Luxembourg · Hextril
  • Latvia · Hexoral
  • Malta · Oraldene
  • Netherlands · Hextril
  • Portugal · Collu-Hextril, Hextril
  • Romania · Hexoral
  • Slovakia · Stopangin

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/e5a081fe-6b66-4145-89ae-edcfbe181c70
GET /v1/drugs/e5a081fe-6b66-4145-89ae-edcfbe181c70?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": "61455112",
  "date_amm": "2012-04-19",
  "type_amm": "Procédure nationale",
  "numero_ue": null,
  "substance": "HEXÉTIDINE",
  "statut_amm": "Autorisation active",
  "statut_bdm": null,
  "forme_pharmaceutique": "solution pour bain de bouche",
  "voies_administration": "voie buccale autre",
  "etat_commercialisation": "Commercialisée",
  "surveillance_renforcee": "Non"
}

See everything about hexétidine.

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.