SEA LEGS

Riik: Iirimaa

keel: inglise

Allikas: HPRA (Health Products Regulatory Authority)

Toimeaine:

MECLOZINE HYDROCHLORIDE

Saadav alates:

GR Lane Health Products Ltd

ATC kood:

R06AE05

INN (Rahvusvaheline Nimetus):

MECLOZINE HYDROCHLORIDE

Annus:

12.5 Milligram

Ravimvorm:

Tablets

Retsepti tüüp:

Product not subject to medical prescription

Terapeutiline ala:

meclozine

Volitamisolek:

Not Marketed

Loa andmise kuupäev:

2000-07-21

Toote omadused

SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
Sea-Legs Tablets.
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each tablet contains 12.50mg Meclozine Hydrochloride.
Also contains 132.6 mg lactose monohydrate.
_For a full list of excipients, see section 6.1._
3 PHARMACEUTICAL FORM
Tablet.
White, round biconvex tablet with a scoreline on one side.
4 CLINICAL PARTICULARS
4.1 THERAPEUTIC INDICATIONS
The prevention and treatment of motion sickness.
4.2 POSOLOGY AND METHOD OF ADMINISTRATION
Route of administration: Oral
Adults and Children over 12 years
Two tablets (25mg) per 24 hours.
The tablets may be taken one hour prior to commencement of journey or,
as Sea-
Legs can remain active for 24 hours after one dose, the previous
night.
Children 6-12 years of age
One tablet (12.5mg) per 24 hours.
Children 2-6 years of age
Half of one tablet (6.25mg) per 24 hours.
4.3 CONTRAINDICATIONS
Contraindicated in pregnancy.
4.4 SPECIAL WARNINGS AND PRECAUTIONS FOR USE
May cause drowsiness, if affected do not drive or operate machinery.
Avoid alcoholic drink.
Sea legs tablets contain Lactose and therefore should not
be taken by patients with rare hereditary problems of
galactose intolerance, the Lapp lactase deficiency or
glucose-galactose malabsorption.
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4.5 INTERACTION WITH OTHER MEDICINAL PRODUCTS