? Tablets are sublanguage homeopathic round, flat-cylindrical, with a risk on one side and with a facet on both sides, from white to light yellow with darker patches;weight of the tablet 250 mg.
1 tab.
Aconitum soongaricum D1 (Aconitum suragaricum) 2.3 mg
Verbascum densiflorum D1 (Verbascum densiflorum) 2.3 mg
Alchemilla vulgaris D1 (Alchemilla vulgaris) 2.3 mg
Echinacea purpurea D1 (Echinacea purpurae) 2.3 mg
Mentha piperita D1 (Menta piperita) 2.3 mg
Daphne mezereum (Mezereum) D1 (Daphneh meseraum) 2.3 mg
Apis mellifica (Apis) D1 (Apis mellica) 2.3 mg
Atropa belladonna (Belladonna) D1 (Atropa belladonna) 2.3 mg
Bryonia dioica D1 (dioic bryonium) 2.3 mg
Hydrargyri dichloridum (Hydrargiri dichloridum) 0.00025 mg
[PRING] sucrose 225.55 mg, gelatin 1.25 mg, calcium stearate 2.5 mg.
10 pieces. - packings cellular planimetric (3) - packs cardboard.
30 pcs. - packings of cellular contour (1) - packs cardboard.
INSTRUCTION FOR THE SPECIALIST.
Description of the drug approved by the manufacturer for the printed edition of 2011.
PHARMACHOLOGIC EFFECT
A multicomponent homeopathic preparation, the effect of which is due to the components that make up its composition.
INDICATIONS
For prophylaxis and as part of complex therapy as a symptomatic agent for "cold" diseases (ARVI) and influenza states (fever, general weakness, headache) in order to increase the nonspecific resistance of the organism.
DOSING MODE
One tablet of the drug is placed under the tongue and held in the mouth until completely dissolved. For treatment in the first 2-3 days apply 1 tablet every 2 hours (7-8 times a day). After lowering the temperature for the next 2-3 days, use 1 tablet 4 times a day. The course of treatment is 5-6 days.
For prevention during the outbreak of acute respiratory viral infection, the drug is taken 1 tablet 4 times a day.
SIDE EFFECT
Allergic reactions are possible.
CONTRAINDICATIONS
Hypersensitivity to the components of the drug, age to 18 years.
PREGNANCY AND LACTATION
Application during pregnancy and during breastfeeding is possible if the expected benefit to the mother exceeds the potential risk to the fetus and the baby. It is necessary to consult a doctor.
APPLICATION FOR CHILDREN
Contraindicated: age to 18 years.
SPECIAL INSTRUCTIONS
The drug does not affect the ability to drive vehicles and engage in other potentially hazardous activities that require increased concentration and speed of psychomotor reactions.
Information for patients with diabetes: one tablet contains 225.55 mg sucrose (sugar-refined), which corresponds to 0.019 XE (bread units). Before using the drug, you should consult your doctor.
OVERDOSE
So far, no cases of overdose have been reported.
DRUG INTERACTION
When using the drug, interaction with other drugs has not been identified.
TERMS OF RELEASE FROM PHARMACY
The drug is approved for use as a means of OTC.
TERMS AND CONDITIONS OF STORAGE
In a dry, protected from light place at a temperature of no higher than 25 В° C. Keep out of the reach of children.
Shelf life. 5 years. Do not use after the expiration date.
