Nux Vomica-Homacord oral drops dropper bottle 30 ml

Instructions for Nux Vomica-Homacord oral drops, dropper bottle 30 ml

Composition

active substances: 100 g of the drug contains: Bryonia D30 - 0.2 g, Bryonia D200 - 0.2 g, Bryonia D1000 - 0.2 g, Bryonia D2 - 0.2 g, Bryonia D6 - 0.2 g, Bryonia D10 - 0.2 g, Bryonia D15 - 0.2 g, Citrullus colocynthis D3 - 0.3 g, Citrullus colocynthis D10 - 0.3 g, Citrullus colocynthis D30 - 0.3 g, Citrullus colocynthis D200 - 0.3 g, Lycopodium clavatum D10 - 0.3 g, Lycopodium clavatum D30 - 0.3 g, Lycopodium clavatum D200 - 0.3 g, Lycopodium clavatum D1000 - 0.3 g, Lycopodium clavatum D3 - 0.3 g, Strychnos nux-vomica D30 - 0.2 g, Strychnos nux-vomica D15 - 0.2 g, Strychnos nux-vomica D10 - 0.2 g, Strychnos nux-vomica D200 - 0.2 g, Strychnos nux-vomica D1000 - 0.2 g, Strychnos nux-vomica D2 - 0.2 g;

excipients: ethanol 96%, purified water.

The drug contains 35% by volume of ethanol 96%.

1 ml of the drug contains 21 drops.

Dosage form

Oral drops.

Main physicochemical properties: clear colorless solution with the smell of ethanol.

Pharmacotherapeutic group

A complex homeopathic preparation.

Pharmacological properties

The drug has an anti-inflammatory, detoxification, antispasmodic and choleretic effect, which is based on the activation of the body's defenses and the normalization of impaired functions due to substances of plant and mineral origin that are part of the drug.

Indication

Functional disorders and inflammation of the gastrointestinal tract, gallbladder and liver, spastic constipation, ulcerative colitis, diverticulitis, gastritis and duodenitis (acute and chronic), stomach ulcer, intestinal dysbiosis, flatulence.

Contraindication

Individual sensitivity to any components of the drug.

Interaction with other medicinal products and other types of interactions

If it is necessary to use any other medicines at the same time, you should consult a doctor.

Application features

At the beginning of treatment with the drug, a short-term exacerbation of existing symptoms of the disease (primary reaction) is possible. This reaction is usually temporary. If the symptoms do not disappear, the drug should be discontinued and a doctor should be consulted.

In rare cases, homeopathic initial exacerbation may lead to temporary dizziness and headache, which resolves quickly and does not require discontinuation of the drug.

This medicinal product contains 35 vol. % ethanol (alcohol), i.e. 138 mg/dose, equivalent to 4 ml beer, 2 ml wine per dose.

Harmful for patients with alcoholism. Caution should be exercised when used in pregnant and breastfeeding women, children, and patients with liver disease and epilepsy.

Use during pregnancy or breastfeeding

This medicine should be used with caution during pregnancy and breastfeeding. The question of the appropriateness of using the medicine in pregnant and breastfeeding women is decided by the doctor individually. There are no data on fertility.

Ability to influence reaction speed when driving vehicles or other mechanisms

Unknown.

Method of administration and doses

Single dose:

children from 2 to 6 years old – 5 drops 3 times a day;

children from 6 to 12 years old, 7 drops 3 times a day;

Adults and children over 12 years old: 10 drops 3 times a day before meals or 1 hour after meals. Dissolve the drops in 10 ml of water and drink, holding in the mouth for a few seconds.

In acute cases:

children from 2 to 6 years old – 5 drops every half hour, but no more than 8 times a day;

children from 6 to 12 years old – 7 drops every half hour, but no more than 8 times a day;

Adults and children over 12 years old – 10 drops every half hour, but no more than 8 times a day.

Dissolve the drops in 10 ml of water and drink, holding in your mouth for a few seconds.

If symptoms persist for more than 7 days or if the condition worsens, treatment should be discontinued and a doctor should be consulted.

The duration of use of the drug depends on the severity and course of the disease and is determined by the doctor individually.

Children.

The drug is recommended for use in children from 2 years of age.

Overdose

It was not noted.

Side effects

In individuals with increased individual sensitivity to the components of the drug, allergic reactions such as urticaria and itching are possible.

If any adverse reactions occur, discontinue use of the drug and consult a doctor.

Expiration date

5 years.

The expiration date determines the use of the drug until the last day of the month.

Storage conditions

Does not require special storage conditions.

Keep out of reach of children.

Packaging

The cardboard box contains a 30 ml glass dropper bottle.

Vacation category

Without a prescription.

Producer

Biologische Heilmittel Heel GmbH.

Address

Dr. Reckeweg-Str. 2-4, 76532 Baden-Baden, Germany/Dr. Reckeweg-Str. 2-4, 76532 Baden-Baden, Germany.