France / CIS 62679978

LANSOYL SANS SUCRE 78,23 g %, gel oral en pot édulcoré à la saccharine sodique

gel · orale

Directory source checks passedOriginal source language: French

Source data retrieved: 2026-09-17. Clinical review is not yet available.

Formgel
Routeorale
Ingredient entries1
CountryFrance

Product identity

At a glance

Authorisation holder
KENVUE FRANCE
Authorisation status
Autorisation active
Market status
Commercialisée
Country
France
Source reference
CIS 62679978

Reported market status does not confirm current pharmacy stock.

From the official composition record

Ingredients & strength

Source entries are shown individually. An active substance (SA) and its reference moiety (FT) may describe the same ingredient; do not add their strengths together.

Source composition entries for LANSOYL SANS SUCRE 78,23 g %, gel oral en pot édulcoré à la saccharine sodique
IngredientStrength / referenceSource role
PARAFFINE LIQUIDEgel78,230 g100 g de gelée oraleSAGroup 1

Pack references

Presentations (1)

1 pot(s) en verre de 215 g

CIP13 3400933234072

Présentation active · Déclaration de commercialisation

From the French medicines authority

Official documents

The official product entry provides access to the patient leaflet and professional product information when available. Documents are in French and availability varies by medicine.

Open the official product entryBDPM · CIS 62679978 · Opens in a new tab

Check the medicine name, strength and form against your pack. The authority’s current documents may be newer than the catalogue snapshot shown here.

Where this information comes from

Sources & dates

Base de données publique des médicaments (BDPM), France. Retrieval dates record when we obtained the source files; they are not clinical review dates or a guarantee of current stock.

Source files and their retrieval dates
Source fileRetrievedSource file modified
fr_products.txtNot supplied
fr_composition.txtNot supplied
fr_packs.txtNot supplied

Directory source checks cover the factual catalogue record.Molindra clinical guidance has not yet been reviewed or published for this medicine.

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