CLARIVER TOUX SANS SUCRE 120 ml FR

Organization name

Labomar S.p.A.

SRN

IT-MF-000007965

Manufacturer status

Active

Certificate health across this manufacturer's portfolio.

1 warning recorded — scroll inside the panel to see all entries.

• CW999

  - Do not take it if you are allergic or hypersensitive to any component. - Do not use the product after the expiry date printed on the package. - Keep out of children's reach. - Shake the stick pack (or bottle) before use. - Wash carefully the measuring cup after use (bottle package only) - Close the bottle accurately after use (bottle package only) - The period of validity after the first opening of the syrup is 3 months (12 weeks) [bottle package only] - Do not use in case the packaging is not intact or damaged; - The syrup has been specifically dosed for children from 3 years old, do not administer to children under 3 years of age. - If you do not notice appreciable results after a short period of treatment (7 days), contact your doctor; in any case do not use for more than 15 days. - So far, no side effects have been observed as a result of the administration of the device. However, if you notice the appearance of side effects, inform your doctor or pharmacist. - The expiry date refers to the packaged product intact, properly stored. - Once the stick pack has been opened, use all its content (stick pack package only)

Primary placement in France; available across 1 country total.

Trade name

CLARIVER TOUX SANS SUCRE 120 ml FR

UDI-DI code

D-FTP096FC

Basic UDI-DI

B-FTP096FC

Reference / catalog number

FTP096

Issuing entity

EUDAMED

Risk category

Class IIa

Applicable legislation

MDD [Directive 93/42/EEC on medical devices]

Status

On the market

Quantity

1

Additional product description

CLARIVER TOUX SANS SUCRE is a medical device designed for the treatment of dry and wet cough and sore throat.

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

European Medical Device Nomenclature — the EU product classification assigned to this device.

• V9017ORAL ADMINISTRATION PREPARATIONS NOT INCLUDED IN OTHER CLASSES