FTP080

Organization name

Labomar S.p.A.

SRN

IT-MF-000007965

Manufacturer status

Active

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

• CW999

  • Consult your doctor if symptoms persist after a week of use, in any case do not use for more than 15 days. • Close the bottle accurately after use. • 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 the reach of children. • Wash carefully the measuring cup after use. • Do not use in case the package is not intact. • The expiry date refers to the product in intact package, properly stored. • In case of concomitant drug therapy, although no interactions with drugs are known, it is recommended to take the product one hour away from other drugs. • There is no clinical evidence available relating to the use of the product during pregnancy or breastfeeding, for this reason its use in these circumstances cannot be recommended. If in doubt consult your doctor. The shelf life after the first opening of the syrup is 4 months (120 days).

Primary placement in Poland; available across 1 country total.

Trade name

not provided

UDI-DI code

D-FTP080_5K6

Basic UDI-DI

B-FTP080_5K6

Reference / catalog number

FTP080

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

FERVEX PHYTO kaszel i gardło (FERVEX PHYTO Mixed Cough) is a medical device composed of substances, not sterile, intended for short term invasive contact with respect to body orifices (oral cavity), designed for the treatment of dry, productive, allergic, tickling cough and sore throats in children (2+) adolescents and adults.

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

D-FTP080_5K6

DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.

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

• V9017ORAL ADMINISTRATION PREPARATIONS NOT INCLUDED IN OTHER CLASSES

Certificate health across this manufacturer's portfolio.