Pharmacy Guide

Patient leaflets and SmPCs, drug interaction checker, official dosages and NHS pharmacy opening hours — all in one place.

Pharmacy Guide

Patient leaflets and SmPCs, drug interaction checker, official dosages and NHS pharmacy opening hours — all in one place.

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Covonia Catarrh Relief Formula

⚠ This medicine appears to have been discontinued

The electronic medicines compendium (emc) no longer publishes a Summary of Product Characteristics for this product, which usually means it is no longer marketed in the UK. The patient leaflet below is kept for reference, but the product may not be available.

If you were prescribed this medicine, other products containing Burdock root liquid extract, Hyssop liquid extract may still be available. Do not stop your treatment — ask your pharmacist or GP what to use instead.

Active substance: Burdock root liquid extract, Hyssop liquid extract
Source: electronic medicines compendium (emc)
Official leaflet: Read the PIL on emc

How to take it

this medicine

HD7 5QH, UK. Covonia is a trade mark of Thornton & Ross Ltd

on THR Certification Mark

If you would like a version of this leaflet in an alternative format, please call 01484 842217

6. Further information What is in this medicine The active ingredients per 5ml are: liquid extract burdock root (Arctium lappa L.)

0.25ml, liquid extract hyssop herb (Hyssopus officinalis L.) 0.35mi.

23440908

Possible side effects

Taking other medicines

any other medicines, including any bought

A

Driving and using machines

This medicine contains ethanol (alcohol). See section 2 "Important information about

some of the ingredients'. If affected by alcohol do not drive or operate machinery.

Like all medicines Covonia Catarrh Relief Formula can have side effects, although these don't affect everyone.

Turn over > 23440908

The other ingredients are: ethanol, methyl parahydroxybenzoate (E218), propyl parahydroxybenzoate, capsicum tincture (containing capsicum oleoresin, ethanol and

purified water), caramel (E150), glycerol (E422), viscarin SD389 (containing dextrose and carageenan (E407)), menthol, sodium saccharin

(E954) and purified water. What the medicine looks like Covonia Catarrh Relief Formula is a brown

cloudy liquid. It is supplied in 100ml and 150ml bottles.

Traditional Herbal Registration holder

and manufacturer

5. Storing this medicine

This leaflet was revised in August 2014

last day of that month.

Adults and the elderly

Tell your doctor or pharmacist if you are taking

Thornton and Ross Ltd., Huddersfield,

¢ Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of any unused medicine. These measures will help to protect the environment.

Oo

¢ Take one 5ml spoonful three times a day. ¢ Do not exceed the stated dose.

doctor before taking this medicinal product.

By reporting side effects you can help provide more information on the safety of this medicine.

¢ Keep it out of the sight and reach of children. ¢ Do not store above 25°C. e Use within 28 days of first opening. ¢ Do not use after the expiry date shown on the carton and bottle. The expiry date refers to the

For oral use only. Shake the bottle before use.

If you miss a dose, take your next dose at the usual time. Do not take a double dose to make up for the missed dose. Consult your doctor or

or any other ingredients listed in section 6.

The following side effect has been reported with burdock root.

Frequently asked questions about Covonia Catarrh Relief Formula

What is the active substance in Covonia Catarrh Relief Formula?

The active substance in Covonia Catarrh Relief Formula is burdock root liquid extract, hyssop liquid extract.

Where does this information come from?

This leaflet reproduces the patient information leaflet approved for Covonia Catarrh Relief Formula, as published on the electronic medicines compendium (emc). The version printed inside your medicine’s packaging is the one that applies to you.

Can I get Covonia Catarrh Relief Formula without a prescription?

Whether a medicine is available over the counter or on prescription only depends on its licence. Check the leaflet, or ask your pharmacist — they can tell you straight away.

About this leaflet

The text above reproduces the patient information leaflet approved for this medicine, restructured for easier reading.

  • Source: electronic medicines compendium (emc), Datapharm
  • Active substance: burdock root liquid extract, hyssop liquid extract
  • Official document: view the original leaflet on emc →
Medical disclaimer: This page is for information only and does not replace advice from your doctor or pharmacist. Always read the leaflet supplied with your medicine. If you are unwell, call NHS 111; in an emergency, call 999.

Medicines with the same active substance: Burdock root liquid extract, hyssop liquid extract (1 medicine)
See every medicine containing this substance, or browse the full A–Z of active substances.
⚕For healthcare professionals — Summary of Product Characteristics (SmPC)Full SmPC: dosage, interactions, contraindications, warnings+
Technical information intended for healthcare professionals (doctors and pharmacists). The Summary of Product Characteristics (SmPC) is the official document approved by the MHRA/EMA. It does not replace the patient leaflet or a doctor’s advice.

4.1. Therapeutic indications

A traditional herbal medicinal product used to relieve the symptoms of nasal catarrh and catarrh of the throat based on traditional use only.

4.2. Posology and method of administration

For oral use only.

Adults and the Elderly: One 5ml spoonful three times a day.

The use in children and adolescents under 18 years of age is not recommended (see section 4.4 “Special warnings and precautions for use”).

Duration of use:

Do not use for more than one week.

4.3. Contraindications

Hypersensitivity to the active substances, other plants of the Asteraceae (Compositae) family or to any of the excipients.

4.4. Special warnings and precautions for use

Do not exceed the stated dose.

This medicinal product contains 11.5vol% ethanol (alcohol), i.e. up to 453 mg per dose, equivalent to 12 ml beer, 5 ml wine per dose.

Harmful for those suffering from alcoholism.

To be taken into account in pregnant or breast-feeding women, children and high-risk groups such as patients with liver disease, or epilepsy.

This medicinal product contains 3.75 mg dextrose (glucose). Patients with rare glucose-galactose malabsorption should not take this medicine.

This medicinal product contains methyl and propyl hydroxybenzoates and may cause allergic reactions (possibly delayed).

The use in children and adolescents under 18 years of age is not recommended due to lack of adequate data and the alcohol content.

If symptoms worsen or persist for more than one week, a doctor or a qualified healthcare practitioner should be consulted.

If dyspnoea, fever or purulent sputum occurs, a doctor or a qualified healthcare practitioner should be consulted.

4.5. Interaction with other medicinal products and other forms of interaction

Contains alcohol and should therefore be avoided in patients taking other medication known to interact with alcohol e.g. Metronidazole.

4.6. Fertility, pregnancy and lactation

Safety during pregnancy and lactation has not been established. In the absence of sufficient data, the use during pregnancy and lactation is not recommended.

Studies on fertility have not been performed.

4.7. Effects on ability to drive and use machines

No studies on the effect on the ability to drive or operate machines have been performed.

This product contains alcohol (see section 2).

4.8. Undesirable effects

Anaphylactic shock has been reported with Burdock root. The frequency is not known.

If other adverse reactions not mentioned occur, a doctor or a qualified healthcare practitioner should be consulted.

Reporting of suspected adverse reactions

Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme at: www.mhra.gov.uk/yellowcard.

4.9. Overdose

No cases known.

Overdose of this product may result in alcohol intoxication. The amount of alcohol in a full bottle (9.06gm in 100ml; 13.59gm in 150ml equivalent to 0.4 and 0.6 large glasses of wine, respectively) may result in alcohol intoxication and should be treated accordingly.

💬 Ask about this leaflet

Ask anything about Covonia Catarrh Relief Formula. The assistant answers only from this leaflet — if the leaflet does not cover it, it will say so. It does not give medical advice.

Answers come from the patient leaflet published on the electronic medicines compendium (emc). They are not medical advice. Ask a pharmacist or your GP if you are unsure. For urgent help call NHS 111, or 999 in an emergency.

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