Echinacea Angustifolia Homeopathic mother tincture Boiron drops 125 ml bottle available in pharmacies. Homeopathic medicine traditionally used in the treatment of colds and associated symptoms such as sore throat.
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ECHINACEA ANGUSTIFOLIA Homeopathic mother tincture Boiron drops
Authorized drug: Aut. 0678
Listed in the pharmacopoeia
PHARMACEUTICAL FORM: Oral liquid.
Therapeutic indications: Homeopathic medicine traditionally used in the treatment of colds and associated symptoms such as sore throat.
Method of administration of ECHINACEA ANGUSTIFOLIA
Oral drops solution for oral use. The drops are to be diluted in a little water.
Posology and method of administration: Medicinal product reserved for adults and children over 12 years old.
Dosage: Children over 12 years old: 1 drop per kg per day to be divided into 3 doses for children from 12 years to 18 years old, without exceeding 15 to 30 drops 3 times per day, to be diluted in a little water. Adult: 15 to 30 drops 3 times a day, to be diluted in a little water. The duration of treatment should not exceed 1 week. Space out as soon as the symptoms improve and stop taking them as soon as the symptoms disappear.
Method of administration: Oral route.
Composition of ECHINACEA ANGUSTIFOLIA
ECHINACEA ANGUSTIFOLIA mother tincture.
Precautions for use of ECHINACEA ANGUSTIFOLIA
Keep out of the reach of children. Due to the presence of alcohol, tell your doctor if you have liver disease, epilepsy or pregnancy. If the symptoms persist, consult your doctor.
Contraindications: Child under 12 years old. Hypersensitivity to the active substance, to other plants of the Asteraceae family or to ethanol.
Warning with ECHINACEA ANGUSTIFOLIA
This medicine contains alcohol. Its alcoholic strength is 55% V / V, or 0.45 g of alcohol for 50 drops.
ECHINACEA ANGUSTIFOLIA leaflet
ECHINACEA ANGUSTIFOLIA TINTURE MOTHER BOIRON, oral liquid. QUALITATIVE AND QUANTITATIVE COMPOSITION: Echinacea angustifolia mother tincture, for a 125ml bottle and syringe for oral administration. Excipient with known effect: Ethanol 55% V / V.
Special warnings and precautions for use: This medicinal product contains 55% V / V of ethanol (alcohol), that is to say 260 mg of alcohol for 30 drops, which is equivalent to 6.6 ml of beer, 2.7 ml of wine per serving. Dangerous if used by alcoholics. To be taken into account in children and high risk groups such as patients with hepatic impairment or epilepsy. This medicine should not be used in pregnant and breastfeeding women. In the event of repeated use, the maximum total duration of treatment should be limited to 6 months.
Fertility, pregnancy and lactation: This medication should not be used during pregnancy and lactation.
Adverse effects: Declaration of suspected adverse reactions: The declaration of suspected adverse reactions after authorization of the drug is important. It allows continuous monitoring of the benefit / risk ratio of the medicinal product. Healthcare professionals report any suspected adverse reactions via the national reporting system: National Agency for Medicines and Health Products Safety (ANSM) and network of Regional Pharmacovigilance Centers - Website: www.signalement-sante.gouv.fr . PHARMACOLOGICAL PROPERTIES: Pharmacodynamic properties: Pharmacotherapeutic group: Homeopathic medicine. In the absence of scientific data, the indication of this drug is based on the traditional homeopathic use of its components.
List of excipients: 96 percent V / V ethanol, purified water.
Shelf life: 3 years before opening. 6 months after first opening.
Special storage precautions: No special storage precautions.
Nature and contents of container: Cardboard box containing a 125 ml vial and a graduated syringe for oral administration.
Special precautions for disposal and handling: No special requirements.
MARKETING AUTHORIZATION HOLDER: BOIRON - 2 avenue de l'Ouest Lyonnais - 69510 Messimy - France.
MARKETING AUTHORIZATION NUMBER: 34009 301 406 5 9: 1 vial of 125 ml and syringe for oral administration.
PRESCRIPTION AND SUPPLY CONDITIONS: Medicinal product not subject to medical prescription. No refund. Dry. Soc. Not approved for communities.
DATE OF FIRST AUTHORIZATION / RENEWAL OF THE AUTHORIZATION: 20/12/2018.
TEXT UPDATE DATE: 07/24/2019