FEMALIFE

  • ABOUT PRODUCT
  • INSTRUCTIONS
COMPOSITION AND PACKING

Round tablets of herbs, with individual odor, biconvex, light – brown, speckled tablets. 60 pieces 0.5 g each. Polyethylene vials with a protective seal or packed in blisters. (1) – cardboard pack with protective holographic label, (2) – instruction for use.

Composition:

Lemon balm (Melissa officinalis L.)
The common fennel (Fructus Foeniculi)
Breckland thyme (Herba Serpylli)
Anise fruits (Fructus Pimpinella anisum L.)

EFFECT OF THE MEDICINE
  • one of the few natural products developed to preserve and maintain breastfeeding with insufficient lactation.
  • contributes to the extension of the period of natural breastfeeding, leads to an early recovery of the organism of the breastfeeding woman in the postpartum period and supports it during feeding.
  • The basis of FEMALIFE is herbs and their seeds, which have long been used in folk medicine with a lack of milk from breastfeeding women.
SIDE EFFECTS

Usually, side effects do not occur, in most cases, the medication is well tolerated.

There may be allergic reactions (itching, rash), as well as nausea, headache, a feeling of bitterness in the mouth. Use of the medicine should be discontinued when hypersensitivity reactions occur and consult a doctor.

SPECIAL INSTRUCTIONS

After opening the vile, store in a cool place.

INTERACTION WITH OTHER MEDICATIONS

When prescribing with other medication adverse effects were not revealed.

INDICATIONS
  • Increases lactation and replenishes the lack of vitamins and minerals in the body of a woman during breastfeeding;
  • Possesses antibacterial and pronounced antioxidant effect;
  • Helps relieve stress and fatigue;
  • Strengthens the immune system;
CONTRAINDICATIONS

Hypersensitivity to some components of the medicine.

DOSAGE

The duration of treatment and the dose are determined by the attending physician for each patient individually.

INSIDE

2 tablets 2-3 times a day, half an hour before meals.

Duration is not limited (usually for the entire period of breastfeeding the baby).

OVERDOSE

The cases of overdose were not reported.

STORAGE CONDITIONS AND EXPIRATION DATE

The medicine should be stored out of reach of children, protected from light, at a temperature from + 2° C to + 25°C.

Expiration date: 24 months

The information presented on the site should not be used for self-diagnosis and treatment and can not serve as a substitute for a doctor's internal consultation.

3

DOLGOJITEL №5

  • ABOUT PRODUCT
  • INSTRUCTIONS

DOLGOJITEL №5 – FOR PEOPLE WITH PHYSICAL DISABILITIES

COMPOSITION AND DOSAGE FORM

DOLGOJITEL № 5, 0.25 gr. in each capsules, 60 pcs of capsules packaged in original bottles with a protective seal. (1) – cardboard pack with protective holographic label, (2) – instruction for use.

Composition:

Dihydroquercetin (Taxifolin) 92% 50 mg.
Arabinogalactan 140 mg.
Starch 60 mg.
EFFECT OF THE MEDICINE
  • The preparation is intended for people with physical disabilities and for those who have to lead a sedentary lifestyle.
  • Dihydroquercetin and arabinogalactan help to ensure the normal functioning of the body, deprived of the natural possibilities.
  • This complex increases vitality, thereby improving the quality of life and increasing its endurance.
SIDE EFFECTS

Usually, there are no side effects; in the majority of cases, the drug is well tolerated.
Use of the drug should be discontinued when hypersensitivity reactions occur.

CONTRAINDICATIONS

Hypersensitivity to one or more components of the drug.

INTERACTION WITH OTHER MEDICATION

When prescribing with other medication adverse effects were not revealed.

INDICATION

As a means of prevention:

During immunity disorders:

  • recommended as a tonic to enhance the body’s defenses;
  • increases the body’s resistance to infectious diseases and the harmful effects of the environment.

During exacerbation and complication of inflammatory diseases:

  • reduces the severity of inflammatory processes;
  • staves off exacerbations and recurrence of chronic inflammatory diseases.

In cardiovascular diseases:

  • contributes to the normalization of blood pressure;
  • improves blood microcirculation and cerebral circulation;
  • reduces the effects of hypoxia and ischemia.
Dosage and Administration

The duration of treatment and the dose are determined by a physician for each patient individually.

PATIENTS BETWEEN 3 AND 9 YEARS OF AGE

PATIENTS BETWEEN 9 AND 18 YEARS OF AGE

PATIENTS ABOVE 19 YEARS OF AGE

1 capsule 1 time a day with meals.

1 capsule 2 times a day with meals.

1 capsule 3 times a day with meals.

Duration of admission

4-8 weeks.

Repeated course after 2 weeks.
Consult with your doctor before use.

STORAGE CONDITIONS AND EXPIRATION DATE

The medicine should be stored out of reach of children, protected from light at a temperature from + 2° C to + 25°C.
Expiration date: 24 months

Not considered as a pharmaceutical medicine.

The information presented on the site should not be used for self-diagnosis and treatment and can not serve as a substitute for a doctor's internal consultation.

3

DOLGOJITEL №2

  • ABOUT PRODUCT
  • INSTRUCTIONS

DOLGOJITEL №2 – RESTORATIVE

COMPOSITION AND DOSAGE FORM

DOLGOJITEL № 2, 0.25 gr. in each capsule, 60 pcs of capsules packaged in original bottles with a protective seal. (1) – cardboard pack with protective holographic label, (2) – instruction for use.

Composition:

Dihydroquercetin (Taxifolin) 92% 45 mg.
Acidum ascorbinicum 25 mg.
Starch 180 mg.
INDICATIONS
  • Restorative agent, indispensable for any person in a modern rhythm of life;
  • General languor, a decrease in physical and intellectual performance, absent-mindedness, depression – these are signs of inadequate tissue supply with nutrients and oxygen as well as an insufficient rate of excretion of degraded products.
  • Dihydroquercetin and its derivatives, through strengthening tissues of blood vessels, contribute to the restoration of their transport function and the disposal of “manager’s syndrome”;
  • Taxifolin is an excellent preventive agent for slowing down the aging process in the body.
SIDE EFFECTS

Usually, there are no side effects; in the majority of cases, the drug is well tolerated.
Use of the drug should be discontinued when hypersensitivity reactions occur.

CONTRAINDICATIONS

Hypersensitivity to one or more components of the drug.

INTERACTION WITH OTHER MEDICATION

When prescribing with other medication adverse effects were not revealed.

INDICATION

In case of immunity disorders:

  • It is recommended as a tonic to strengthen the body’s defenses, resistance to infectious diseases and the harmful effects of the environment.

In exacerbations and complications of inflammatory diseases:

  • resistance improves, the severity of the inflammatory process reduces, the exacerbation and recurrence of chronic inflammatory diseases stave off.

In the course of liver dysfunction when it is impaired:

  • the functional condition of the liver cells improves, and its antitoxic function will be maintained.

In varicose veins, phlebothrombosis, with post-thrombophlebitic syndrome:

  • strengthens the venous walls, improves venous blood flow, prevents thrombosis and reduces edema.

In the complications of diabetes:

  • improves microcirculation, strengthens the capillary bed, reduces insulin resistance, and improves the quality of life.
Dosage and Administration

The duration of treatment and the dose are determined by a physician for each patient individually.

PATIENTS BETWEEN 3 AND 9 YEARS OF AGE

PATIENTS BETWEEN 9 AND 18 YEARS OF AGE

PATIENTS ABOVE 19 YEARS OF AGE

1 capsule 1 time a day with meals.

1 capsule 2 times a day with meals.

1 capsule 3 times a day with meals.

Duration of admission

4-8 weeks.

Repeated course after 2 weeks.
Consult with your doctor before use.

STORAGE CONDITIONS AND EXPIRATION DATE

The medicine should be stored out of reach of children, protected from light at a temperature from + 2° C to + 25°C.
Expiration date: 24 months

Not considered as a pharmaceutical medicine.

The information presented on the site should not be used for self-diagnosis and treatment and can not serve as a substitute for a doctor's internal consultation.

3

NOMAGISSAN

  • ABOUT PRODUCT
  • INSTRUCTIONS
COMPOSITION AND DOSAGE FORM

Round tablets of herbs and their fruits, with individual odor, biconvex, light – brown, speckled tablets. 60 pieces 0.5 g each. Polyethylene vials with a protective seal or packed in blisters. (1) – cardboard pack with protective holographic label, (2) – instruction for use.

Composition:

One-sided-wintergreen (Orthília secúnda L.)
Oregano (Origanum vulgáre L.)
Rose Hips Fruits (Frūctus Rosāe)
Chamomile (Matricāria chamomīlla L.)
Marigold Officinalis (Caléndula officinális L.)
Shepherd’s purse (Capsélla búrsa – pastóris L.)
Sandy Everlast (Helichrýsum arenárium L.).

EFFECT OF THE MEDICINE
  • Combination herbal menstrual cycle regulator.
  • It promotes the elimination of post-menopausal bleeding by stimulating and strengthening the muscles of the endometrium and ovarian tissue.
  • It has anti-inflammatory and antibacterial properties.
  • It helps in premenstrual syndrome, as the medicine monitors and aligns hormone levels.
  • It helps metabolism, restores immunity (protective properties of the body) and has a health improving properties.
SIDE EFFECTS

Usually, there are no side effects; in the majority of cases, the medicine is well tolerated. In the case of individual sensitivity to one or more components of the medicine, there may be allergic reactions, dyspeptic disorders of the gastrointestinal tract.

INTERACTION WITH OTHER MEDICATION

When prescribing with other medication adverse effects were not revealed.

INDICATIONS
  • Dysmenorrhea, amenorrhea, hypermenorrhoea (in the complex therapy);
  • Premenstrual syndrome;
  • Abnormal vaginal discharge;
  • Postmenopausal bleeding;
  • White vaginal discharge caused by blockage of cervical glands (Leucorrhœa);
  • Copious menstruation (Menorrhagia);
  • Uterine bleeding not related to the menstrual cycle (Metrorrhagia).
 CONTRAINDICATIONS

Hypersensitivity to one or more components of the medicine, pregnancy, lactation.

DOSAGE

The duration of treatment and the dose are determined by the attending physician for each patient individually.

ADULTS

2 tablets 3 times a day 5-10 minutes before the meal.

The course of treatment is 15 days.
If necessary, the treatment course can be repeated.

OVERDOSE

The cases of NOMAGISSAN overdose were not reported.

STORAGE CONDITIONS AND EXPIRATION DATE

The medicine should be stored out of reach of children, protected from light, at a temperature from + 2° C to + 25°C.

Expiration date: 2 years.

The information presented on the site should not be used for self-diagnosis and treatment and can not serve as a substitute for a doctor's internal consultation.

3

VITALIT

  • ABOUT PRODUCT
  • INSTRUCTIONS
COMPOSITION AND DOSAGE FORM

Round tablets, biconvex, light – brown, speckled tablets, 60 pieces. Polyethylene vials with a protective seal or packed in blisters. (1) – cardboard pack with protective holographic label, (2) – instruction for use.

Composition:

Bird Cherry Fruits (Fructus Padus)
Rose Hips Fruits (Frūctūs Rosae)
Common Nettle (Urtica dioica L.)
Roseroot (Rhodiola rosae L)
Creeping Thyme (Thymus serpyllum L)
Walnut (Júglans régia)

effect of the medicine
  • VITALIT is a complex herbal vitamin medicine, consisting of vitamins, macro- and microelements and Bifida bacteria.
  • Compensates lack of vitamins and minerals in the body,  and it has antioxidant activity which normalizes intestinal micro-flora and increases a non-specific resistance of the organism.
  • It is recommended as a health improving agent to enhance the body’s defenses, resistance to infectious diseases and environmental hazards.
  • Contributes to the restoration and maintenance of the normal functioning of the gastrointestinal tract.
  • Helps in asthenic conditions, convalescence after infections and colds and other states, accompanied by vitamin deficiency, including the prevention of hypovitaminosis A, C, P, K (combination therapy).
INDICATIONS
  • The medicine beneficially effects overall health, improves physical and mental health;
  • Prevention of vitamin deficiencies, lack of minerals and micronutrients;
  • Increases the body’s resistance to adverse environmental effects;
  • Strengthens the immune system, it contributes to the prevention of infectious diseases;
  • Stimulates metabolism;
  • Increases the body’s resistance to stress, prevents depression;
  • Promotes excretion of salts of heavy metals and other toxic substances;
  • Compensates the deficiency of vitamins and minerals, caused by physical and mental work, poor nutrition;
  • For the period of pregnancy and lactation;
  • Reduces the negative effects of smoking and alcohol consumption.
INTERACTION WITH OTHER MEDICATION

When prescribing with other medication adverse effects were not revealed.

RECOMMENDATIONS

The medicine is recommended as a multivitamin, health improving agent for the prevention and in the complex therapy of diseases such as:
– Hypertension;
– Atherosclerosis;
– Thyroid gland dysfunction;
– Diabetes;
– Gastritis with low acidity;
– Kidney disease;
– Rheumatism;
– Radiation injuries and allergic diseases of the skin (eczema, dermatitis, neurodermatitis);
– Bleeding of various origins;
– Hypovitaminosis – and vitamin deficiency.

CONTRAINDICATIONS

Hypersensitivity to one or more components of the medicine.

DOSAGE

Dosage is determined individually.

ADULTS

CHILDREN BETWEEN 3 AND 12 YEARS OF AGE

2 tablets 2-3 times a day with the meal

1 tablet 2-3 times a day with the meal

The course of administration is 1-2 months. If necessary the treatment course can be repeated.

SIDE EFFECTS

Usually, there are no side effects. In the majority of cases, the medicine is well tolerated.
In the case of individual sensitivity to one or more components of the medicine, there may be allergic reactions, dyspeptic disorders of the gastrointestinal tract.
Use of the medicine should be discontinued when hypersensitivity reactions occur.

OVERDOSE

The cases of VITALIT overdose were not reported.

STORAGE CONDITIONS AND EXPIRATION DATE

The medicine should be stored out of reach of children, protected from light, at a temperature from + 2° C to + 25°C.
Expiration date: 2 yearsю

The information presented on the site should not be used for self-diagnosis and treatment and can not serve as a substitute for a doctor's internal consultation.

3

IMMUNOROK

  • ABOUT PRODUCT
  • INSTRUCTIONS
COMPOSITION AND PACKING

Syrup of herbal extracts, brown viscous liquid with individual odor (may have light sediment and clouding) in the original vials of 150 ml with a protective seal – (1) cardboard packs with protective branded holographic label; (2) Spoon – dispenser; (3) instruction for use.

Composition:
Rose root Extract (Rhodiola rosea)
Peppermint Extract (Méntha piperíta)
Coneflower Extract (Echinacea purpurea (L.)
Liquorice Extract (Glycyrrhiza glabra)
Rose Hips Extract (Rosa majalis)
Elecampane Extract (Inula helenium)
EFFECT OF THE MEDICINE
  • Immunomodulatory effect of the medicine is achieved by activation of humoral and cellular immunity;
  • Effective against influenza viruses, parainfluenza, herpes viruses, enteroviruses, rotavirus;
  • Stimulates the bactericidal activity of neutrophils;
SIDE EFFECTS

There may be rarely allergic hypersensitivity to separate ingredients of the preparation.
Use of the medicine should be discontinued when hypersensitivity reactions occur.
The usage of the medicine must be informed to the doctor before the surgery.

SPECIAL INSTRUCTIONS

Before use, carefully shake the vial.
Keep the vial in a cool place after opening it. Do not heat and do not freeze.

INTERACTION WITH OTHER MEDICATION

When prescribing with other medication adverse effects were not revealed.

INDICATIONS
  • Asthenic state, neurotic and somatoform disorders;
  • Relieving symptoms of uncomplicated viral and bacterial diseases;
  • The treatment of acute and chronic herpes and cytomegalovirus infections;
  • Reduced physical performance;
  • Prevention and treatment of infections in immunodeficient states;
CONTRAINDICATIONS

Individual intolerance to certain ingredients of the medicine.

DOSAGE

The duration of treatment and the dose are determined by the attending physician for each patient individually.

CHILDREN FROM 1 TO 6 YEARS OF AGE

CHILDREN FROM 7 TO 12 YEARS OF AGE

ADULTS AND CHILDREN ABOVE 12 YEARS OF AGE

1.0-1.5 ml 3 times a day

1.5-2.5 ml 3 times a day

2.5-5.0 ml 3 times a day

For peroral use, 10-15 minutes before the meal.
The medicine should be taken at least 15 days to achieve a therapeutic effect.

OVERDOSE

The cases of overdose were not reported.

STORAGE CONDITIONS AND EXPIRATION DATE

The medicine should be stored out of reach of children, protected from light, at a temperature from + 2° C to + 25°C.
Expiration date: 24 months.

The information presented on the site should not be used for self-diagnosis and treatment and can not serve as a substitute for a doctor's internal consultation.

3

NATUROSED

  • ABOUT PRODUCT
  • INSTRUCTIONS
COMPOSITION AND DOSAGE FORM

Round tablets of herbs, with individual odor, biconvex, light – brown, speckled tablets. 60 pieces 0.5 g each. Polyethylene vials with a protective seal or packed in blisters. (1) – cardboard pack with protective holographic label, (2) – instruction for use.

Composition:

Peppermint (Méntha piperíta)
Oregano (Origanum Vulgare L)
Common Valerian (Valeriána officinális L.)
Cowberry Leaves (Folium vitis-idaea L.)
Creeping Thyme (Thymus serpyllum L.)
Common Motherwort (Leonurus L.)
Hawthorn (Crataegus sanguinea)

EFFECT OF THE MEDICINE
  • improves the central nervous system functioning;
  • contributes to the improvement of the autonomic nervous system;
  • improves the psycho-emotional stability of the body, normalizes sleep;
  • contributes to the preservation of peace stressful situations;
  • strengthens the immune system and increases the body’s defenses.
SIDE EFFECTS

Usually does not occur, in most cases, the drug is tolerated well.
In the case of individual hypersensitivity to one or more of the components of the drug, allergic reactions, dyspepsia disorders on the part of the gastrointestinal tract are possible.
When developing a hypersensitivity reaction, the drug should be discontinued.

INTERACTION WITH OTHER PREPARATIONS

When prescribing with other medication adverse effects were not revealed.

INDICATIONS
  • Functional disorders of the central and autonomic nervous system;
  • The state of prolonged stress, significant mental and emotional stress;
  • Irritability, emotional lability;
  • Chronic fatigue, overwork;
  • Sleep disturbances;
  • Cardioneurosis;
  • Psychosomatic disorders;
  • Climacteric syndrome;
CONTRAINDICATIONS

Hypersensitivity to one or more of the components of the medicine.

DOSage

The duration of treatment and the dose are determined by a physician for each patient individually.

CHILDREN FROM 3 YEARS OF AGE

ADULTS

1 tablet 3 times a day.

1-2 tablets 3 times a day.

In stationary conditions, as an auxiliary sedative effect, 1 tablet 3 times a day.

Tablets are taken 10-15 minutes before meals.

Usually, for chronic diseases, the course of treatment is 20 – 30 days.

If necessary, a second course is possible.

OVERDOSE

No cases of overdose of Naturosed have been detected.

STORAGE CONDITIONS

The drug should be stored out of reach of children, protected from light, at a temperature of +2 ° C to + 25 ° C.

Expiration date: 24 months

The information presented on the site should not be used for self-diagnosis and treatment and can not serve as a substitute for a doctor's internal consultation.

3

ZRENODOL CHERNIKA+

  • ABOUT PRODUCT
  • INSTRUCTIONS
COMPOSITION AND PACKING

Syrup of herbal extracts and their fruits, brown viscous liquid with individual odor (may have light sediment and clouding) in the original vials of 150 ml with a protective seal – (1) cardboard packs with protective branded holographic label; (2) Spoon – dispenser; (3) instruction for use.

Composition:
Blueberry Fruit Extract (Vaccinium myrtillus)
Hawthorn Fruit Extract (Crataegus)
Sweet flag Extract (Acorus calamus)
Rose Hip Extract (Rosa majalis)
EFFECT OF THE MEDICINE
  • ZRENADOL CHERNIKA+ protects the eyes from fatigue, irritation, and vision weakening;
  • improves dark adaptation;
  • reduces the permeability of capillaries, strengthens the walls of blood vessels, including the vessels of the eye fundus, reduces swelling and redness;
  • supports visual organs with essential nutrients – vitamins and micronutrients;
  • Tends to have a positive effect on the functional status of the visual organs associated with the deficiency of vitamins and micronutrients, has a health-promoting effect and is a natural product.
  • Blueberry’s anthocyanosides contribute to the regeneration of the photosensitive pigment of the retina, increasing its sensitivity to changes in light intensity, improving visual acuity during low-light conditions; contributes to the improvement of dark adaptation.
  • Active substances of Blueberry improve the flexibility of cell membranes and help to enhance blood flow to the retina.
  • Blueberry extract and vitamin C (the main component of rose hips) with bioflavonoids promote the blood circulation in the vision organs, reduce intraocular pressure and have strong antioxidant properties, i.e. prevent damage to eye tissue by free radicals. In addition, they have an antimicrobial effect and promote the healing of injuries.
SIDE EFFECTS

There may be rarely allergic hypersensitivity to separate ingredients of the preparation.
Use of the medicine should be discontinued when hypersensitivity reactions occur.

SPECIAL INSTRUCTIONS

Before use, carefully shake the syrup.
Keep the vial in a cool place after opening it. Do not heat and do not freeze.

INTERACTION WITH OTHER MEDICATION

When prescribing with other medication adverse effects were not revealed.

INDICATIONS

ZRENADOL CHERNIKA is applied in the following:

  • as a part of measures to prevent the deterioration of vision organs;
  • at high visual load (work at the computer, long time driving or in bright sunlight);
  • combination treatment of vascular pathologies of the eye (cataract, glaucoma, myopia);
  • for patients with impaired twilight vision (“night blindness”).
CONTRAINDICATIONS

Individual intolerance to certain ingredients of the medicine.

DOSAGE

The duration of treatment and the dose are determined by the attending physician for each patient individually.

CHILDREN BETWEEN 3 AND 7 YEARS OF AGE

CHILDREN BETWEEN 7 AND 14 YEARS OF AGE

ADULTS AND CHILDREN ABOVE 14 YEARS OF AGE

1.5-2.0 ml 2 times a day

2.5 ml 2 times a day

5.0 ml 2 times a day

The medicine is administered with meals with plenty of water.
The course of administration is 1 month. Courses can be repeated after a weak.

OVERDOSE

The cases of overdose were not reported.

STORAGE CONDITIONS AND EXPIRATION DATE

The medicine should be stored out of reach of children, protected from light, at a temperature from + 2° C to + 25°C.
Expiration date: 24 months.

The information presented on the site should not be used for self-diagnosis and treatment and can not serve as a substitute for a doctor's internal consultation.

3