France· FR:60206332
ACTIFED RHUME JOUR ET NUIT, comprimé
A medicinal product, registered in France by KENVUE FRANCE.
Checked against Base de données publique des médicaments — BDPM (France) on
Informational only — not a medical device.
The record
At a glance
Base de données publique des médicaments — BDPM (France)- Manufacturer
- KENVUE FRANCE
- 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
- cip133400935753274plaquette(s) PVC-Aluminium PVDC de 12 comprimé(s) - plaquette(s) PVC-Aluminium de 4 comprimé(s)
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
ACTIFED in 6 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United StatesAcetaminophen and Diphenhydramine citrateInvaTech Pharma Solutions LLC
- United KingdomCalCold Six Plus oral solutionMcNeil Products Ltd
- IrelandDozol Oral Solution Paracetamol 120 mg/5 ml Diphenhydramine Hydrochloride 12.5 mg/5 mlPhoenix Healthcare Ltd
- CanadaACETAMINOPHEN WITH ANTIHISTAMINE NIGHTTIMELABORATOIRES TRIANON INC.
- SpainANTIDOL NOCHE 500 MG/25 MG COMPRIMIDOS RECUBIERTOS CON PELICULALaboratorios Cinfa S.A.
- PolandApap NocUS Pharmacia Sp. z o.o.
Authorised across Europe · EMA
The same active substance is authorised in 6 EEA countries. Names it is sold under:
- Spain · Dolomidina
- United Kingdom (Northern Ireland) · Panadol Night, Panadol Nightpain
- Ireland · Dozol, Panadol Night
- Malta · Dozol, Teedex
- Poland · Apap Noc, Paracetamol + Difenhydramina Noc Hasco
- Portugal · Algik Noite, Chrobion
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/c8f002a8-d2b1-4dc7-b69a-e18bc8219639 GET /v1/drugs/c8f002a8-d2b1-4dc7-b69a-e18bc8219639?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": "60206332",
"date_amm": "2001-08-08",
"type_amm": "Procédure nationale",
"numero_ue": null,
"statut_amm": "Autorisation active",
"statut_bdm": "Warning disponibilité",
"forme_pharmaceutique": "comprimé et comprimé",
"voies_administration": "orale",
"etat_commercialisation": "Non commercialisée",
"surveillance_renforcee": "Non"
}See everything about ACTIFED.
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.