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Texa Allergy is a non-sedating antihistamine used for the relief of allergic conditions such as:
Active ingredient
The active substance is cetirizine dihydrochloride. One ml of Texa Allergy syrup contains 1 mg cetirizine dihydrochloride.
Other ingredients
The other ingredients: acetic acid, banana flavour, glycerol, methyl parahydroxybenzoate, propylene glycol, propyl hydroxybenzoate, purified water, saccharin sodium, sodium acetate and sorbitol 70%.
Preservatives: methyl parahydroxybenzoate and propyl hydroxybenzoate.
Sweeteners (glycerol 200 mg/ml, saccharin sodium 1 mg/ml and sorbitol 70% solution 450 mg/ml)
Suitable for
Adults and children aged 2 and over
Dosage
Adults or children 12 years of age or older:
• 10mg (10ml) once daily.
Children 6 to 12 years old:
• 10mg (10ml) daily, either as a single dose or as divided doses of 5ml in the morning and 5ml in the evening.
Children aged 2 to 6 years:
• 5mg (5 ml) daily, either as a single dose or as divided doses of 2,5ml in the morning and 2,5ml in the evening.
If you have a kidney or liver disorder, take 5mg (5ml) once daily.
Active ingredient
The active substance is cetirizine dihydrochloride (10mg).
Other ingredients
Other ingredients: crospovidone, sugar (lactose monohydrate 117,0 mg), magnesium stearate, microcrystalline cellulose, and silica colloidal anhydrous. Film coating ingredients: microcrystalline cellulose, hypromellose, macrogol stearate, titanium dioxide and propylene glycol.
Suitable for
Adults and children aged 6 and over
Dosage
Adults/ children 12 years or older: 10 mg (one tablet) once daily.
Children 6 – 12 years: 5 mg (half a tablet) twice daily or 10mg (one tablet) once daily.
These articles are for information purposes only. It cannot replace the diagnosis of a healthcare provider. Pharma Dynamics gives no warranty as to the accuracy of the information contained in such articles and shall not, under any circumstances, be liable for any consequences which may be suffered as a result of a user’s reliance thereon.
The information the reader is about to be referred to may not comply with the South Africa regulatory requirements. Information relevant to the South African environment is available from the Company and in the Professional Information/Patient Information Leaflet/Instructions for Use approved by the Regulatory Authority
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