Arnigel® (Arnigel®)

Composition Pharmacodynamics Indications Carefully Contraindications Dosing and Administration Side effects Form release / dosage
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Dosage form: & nbspgSpruce for external use Homeopathic
Composition:

Per 100 g:

Active components: Amica montana (arnica Montana) MT - 7 g;

Auxiliary components: carbomer 0.90 g, sodium hydroxide solution 10% 1.70 g, ethanol 96% 20 g, purified water 70.40 g.

Description:

Transparent, homogeneous gel from yellow to yellow-orange color with a weak odor.

Pharmacotherapeutic group:Homeopathic Remedy
Pharmacodynamics:

One-component homeopathic preparation, the effect of which is due to the component that is part of its composition.

Indications:Contusions, bruises, muscle pain due to excessive physical exertion.
Contraindications:

Increased individual sensitivity to individual components of the drug.

Violation of the integrity of the skin, wetting dermatitis and other skin diseases in the area of ​​presumed application of the drug.

Contraindicated apply to mucous membranes.

Children up to 1 year.

Pregnancy and lactation:

Do not use the drug during pregnancy (due to the lack of clinical data in this category of patients).

The use of the drug in the period of breastfeeding is possible if the expected benefit for the mother exceeds the potential risk for the child. Consultation of the doctor is necessary.

Dosing and Administration:

Outwardly. For children from 1 year and adults, apply a small amount of the gel with a uniform thin layer on the skin of the painful areas and rub it with light massaging movements until completely absorbed.

The procedure should be carried out 1-2 times within 5-7 days.

Side effects:

To date, there has been no information on the side effects of the drug. If side effects occur, consult a doctor.

Allergic reactions are possible.

Overdose:

Cases of drug overdose have not been registered to date.

Interaction:

It is not recommended simultaneous use with anticoagulants of indirect action. The use of homeopathic drugs does not exclude the treatment with other drugs.

Special instructions:

Perhaps the appearance of dryness and irritation of the skin due to the content in the preparation of ethyl alcohol (ethanol).

It is not recommended to apply the gel under the occlusive dressing.

Effect on the ability to drive transp. cf. and fur:The use of the drug does not affect the ability to perform potentially dangerous activities requiring increased concentration and speed of psychomotor reactions (management of transportmeans, work with moving mechanisms, work of the dispatcher and the operator).
Form release / dosage:Gel for external use is homeopathic.
Packaging:

By 45 g or 120 g in an aluminum tube, covered from the inside with epoxy phenol varnish sealed with aluminum foil, with a screwed polyethylene lid.

Each tube together with the instruction for use is placed in a cardboard box.

Storage conditions:

At a temperature of no higher than 25 ° C.

Keep out of the reach of children.

Shelf life:

3 years.

Do not use after the expiration date.

Terms of leave from pharmacies:Without recipe
Registration number:LP-000048
Date of registration:23.11.2010 / 31.03.2017
Expiration Date:Unlimited
The owner of the registration certificate:BUARONBUARON France
Manufacturer: & nbsp
BOIRON France
Representation: & nbspBUARON LLCBUARON LLCFrance
Information update date: & nbsp13.09.2017
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