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France· FR:63713344

HUMEX RHUME, comprimé et gélule

A medicinal product containing paracétamol + chlorhydrate de pseudoéphédrine + maléate de chlorphénamine, registered in France by LABORATOIRES URGO HEALTHCARE.

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…normalisedHUMEX RHUME, comprimé et géluleATC—REGISTER NO.FR:63713344PACKS LISTED1CHECKEDSeptember 12, 2026

The record

At a glance

Base de données publique des médicaments — BDPM (France)
Active substance
PARACÉTAMOL + CHLORHYDRATE DE PSEUDOÉPHÉDRINE + MALÉATE DE CHLORPHÉNAMINE
Manufacturer
LABORATOIRES URGO HEALTHCARE
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
    3400934474637
    12 comprimés et 4 gélules sous plaquette (PVC/Aluminium)

Regulatory notes

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

Same medicine, other countries

Paracétamol + chlorhydrate de pseudoéphédrine + maléate de chlorphénamine in 3 other countries

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

All paracétamol + chlorhydrate de pseudoéphédrine + maléate de chlorphénamine products

Authorised across Europe · EMA

The same active substance is authorised in 8 EEA countries. Names it is sold under:

  • Bulgaria · Tайлол Хот, Tайлол Хот Д
  • Cyprus · Comtrex Cold, Snip
  • Spain · Gelocatil Gripe Con Pseudoefedrina, Vincigrip
  • Greece · Comtrex Cold
  • Croatia · Rhinostop
  • Malta · Snip
  • Poland · Tabcin Trend
  • Romania · Coldrex Sinus Extra, Humagrip

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/b79178a1-0916-4797-880a-fa33505aa3b6
GET /v1/drugs/b79178a1-0916-4797-880a-fa33505aa3b6?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": "63713344",
  "date_amm": "1997-09-22",
  "type_amm": "Procédure nationale",
  "numero_ue": null,
  "substance": "PARACÉTAMOL + CHLORHYDRATE DE PSEUDOÉPHÉDRINE + MALÉATE DE CHLORPHÉNAMINE",
  "statut_amm": "Autorisation active",
  "statut_bdm": "Warning disponibilité",
  "forme_pharmaceutique": "comprimé et  gélule",
  "voies_administration": "orale",
  "etat_commercialisation": "Non commercialisée",
  "surveillance_renforcee": "Non"
}

See everything about paracétamol + chlorhydrate de pseudoéphédrine + maléate de chlorphénamine.

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.