Herbapect 498 mg + 349 mg + 87 mg Syrup 150 g

Herbapect 498 mg + 349 mg + 87 mg Syrup 150 g

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Description

Herbapect 498 mg + 349 mg + 87 mg Syrup 150 g

The most important features of the product
Tiring so-called dry cough, difficult expectoration, sugar-free
Description
(498 mg + 349 mg + 87 mg)/ 5 ml, syrup
Thymi extractum fluidum + Primulae tinctura + Sulfogaiacolum.

Action: Expectorant.
Indications for use: Traditionally in rhinitis of the upper respiratory tract. Tedious so-called "dry cough". Difficult expectoration.

OTC - Medication dispensed without a prescription.
Storage and use
Oral administration. It is necessary to read the contents of the label-leaflet before using the drug, for this purpose, peel off the label in the upper right corner at the place marked with an arrow.

Method of use and route of administration: The package comes with a measuring cup for easy dosage, with which the drug should be measured. Adults: 5 ml of syrup 3 to 4 times a day, after a meal. Children over 4 years and adolescents up to 18 years: 2.5 ml of syrup 3 to 4 times a day after a meal no more often than every 4 hours. This drug should always be used exactly as described on the label or as prescribed by your doctor or pharmacist. The drug should not be used for more than 7 days. If after 7 days. If there is no improvement after 7 days or the patient feels worse, contact your doctor.

Overdose: If you take more than the recommended dose, contact your doctor. If you miss a dose of the drug, take the next dose as soon as possible. Do not use a double dose to make up for a missed dose.
Storage: Store at ambient temperature.
Dimensions: Height: 121 mm. Width: 50 mm. Depth: 50 mm.
Composition
5 ml of syrup contains active substances: 498 mg liquid extract of thyme herb (Thymus vulgaris L., herba) (1:2), extraction solvent: ethanol 30% (V/V), ammonia water 25%, glycerol 95%; 349 mg tincture of primula root (Primula veris L., radix) (1:5) extraction solvent ethanol 70 % (V/V); 87 mg sulfogaiacol (Sulfogaiacolum) once excipients of known effect: liquid sorbitol, non-crystallized (E420), Contains 6.4-9.0 % (V/V) ethanol
Manufacturer
Aflofarm Farmacja Polska Sp. z o.o.
Manufacturer's address
Responsible entity:
Aflofarm Farmacja Polska Sp. z o.o.
Partyzancka street 133/151
95-200 Pabianice,
Tel: (42) 22-53-100
Safety warning
Contraindications: Hypersensitivity to the active substances or to the excipient. Asthma.
Do not use in children who have suffered from acute laryngitis (croup).
Interactions: No data available.
Pregnancy and breastfeeding: Not recommended for use during pregnancy and breastfeeding.
Driving and operating machinery: No data available.

Warnings and precautions:
The drug contains ethanol and liquid sorbitol, not crystallized (E420).
This drug contains 356.85 mg of alcohol (ethanol) in 5 ml of syrup, which is equivalent to 7.14% (w/v). The amount of alcohol in 5 ml of this drug is equivalent to less than 9 ml of beer or 4 ml of wine. a small amount of alcohol in this drug will not cause noticeable effects.
The drug contains 5291.25 mg of liquid non-crystallizable sorbitol, which is equivalent to 3504.924 mg of pure sorbitol in each 5 ml of syrup and is equivalent to 0.21 ww.

Sorbitol is a source of fructose. If you (or your child) have been previously diagnosed with intolerance to certain sugars, or you have been previously diagnosed with hereditary fructose intolerance, a rare genetic disorder in which your body does not break down fructose, you should contact your doctor before taking the drug or giving it to your child. Sorbitol may cause gastrointestinal discomfort and may have a mild laxative effect. Notes for diabetics The syrup does not contain sugar and can be used by diabetics.
Children: Not recommended for use in children under 4 years of age.

Side effects: Like any drug, this medication may cause side effects, although they will not occur in everyone. Possible allergic reactions and gastrointestinal disorders (nausea and vomiting).
Allergic reactions can sometimes be anaphylactic shock or vasomotor edema. If swelling, a sharp drop in blood pressure, bronchospasm or the patient feels unwell, call for medical help immediately.

Reporting side effects
If you experience any side effects, including any side effects not listed in the leaflet, tell your doctor or pharmacist. Adverse reactions can be reported directly to the Adverse Drug Reactions Monitoring Department of the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products: Al. Jerozolimskie 181C, 02-222 Warsaw
Tel: + 48 22 49 21 301, Fax: + 48 22 49 21 309
Website: https://smz.ezdrowie.gov.pl

Adverse reactions can also be reported to the responsible party.
By reporting side effects, more information on the safety of the drug can be gathered.
Keep the drug out of sight and reach of children.
Lower age limit
Recommended: 4 years/years/years

Product Details

5 Items

Specific References

EAN13
5909990663613

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