MOVICOL® Paediatric Plain

Organization name

Norgine BV

SRN

NL-MF-000009565

Manufacturer status

Active

6 warnings recorded — scroll inside the panel to see all entries.

• CW276

  There is a possibility that the absorption and consequently the effectiveness of any medicines taken orally could be reduced if taken at the same time as Movicol Paediatric Plain. Therefore, as a precautionary measure, any medicines should not be given to the child orally for one hour before, during and for one hour after taking Movicol Paediatric Plain. Please consult your doctor or pharmacist if your child is taking, or has recently taken, any medicines, including medicines obtained without a prescription.
• CW999

  If you need to thicken fluids in order for the child to swallow them safely, Movicol Paediatric Plain may counteract the effect of the thickener.
• CW999

  Movicol Paediatric Plain contains sodium. Movicol Paediatric Plain contains 93.4 mg sodium (main component of cooking/table salt) per sachet. This is equivalent to 4.6% of the recommended maximum daily dietary intake of sodium for an adult.
• CW135

  Keep out of the sight and reach of children
• CW032

  Do not use Movicol Paediatric Plain after the expiry date on the sachet and carton.
• CW999

  Do not take Movicol Paediatric Plain if your doctor has told you that the child has: • a blockage in its intestine (gut obstruction, ileus) • a perforated gut wall •severe inflammatory bowel disease like ulcerative colitis, Crohn’s disease or toxic megacolon • an allergy to any of the ingredients of Movicol Paediatric Plain.

Primary placement in Germany; available across 1 country total.

Trade name

MOVICOL® Paediatric Plain

UDI-DI code

05012748605640

Basic UDI-DI

B-05012748605640

Reference / catalog number

77710022 (30er carton)

Issuing entity

GS1

Risk category

Class IIb

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

MOVICOL® Plain, 6.9g Powder for oral solution (30 sachets)

Additional information URL

https://www.norgine.de/

Clinical sizes

• 6.9g powder for oral solution

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

• G0401ORALLY ADMINISTERED DEVICES FOR THE THERAPY OF GASTRO-INTESTINAL DISORDERS

Certificate health across this manufacturer's portfolio.