Klimadinon Bionorica
19,99 $Klimadinon Bionorica 60 tabs
Manufacturer:
Bionorica SE, Germany
Composition of Klimadinon Bionorica
Active ingredient: Black cohosh (Cimicifuga racemosa L.) rhizome dry extract 20.0 mg (contains 2.8 mg of native black cohosh rhizome extract (5-10:1, 58% v/v ethanol extractant) and 17.2 mg of lactose monohydrate). Excipients: calcium hydrogen phosphate dihydrate, potato starch, magnesium stearate, talc, titanium dioxide E 171, iron oxide yellow E 172, iron oxide red E 172, macrogol 6000, Eudragit RL 30D (ammonium methacrylate copolymer (1:2:0.2) 1.35 mg, and sorbic acid 0.01 mg).
Pharmacological action
Klimadynon has an estrogen-like effect, exhibits sedative properties, and has a therapeutic effect on the autonomic nervous system. Its use helps alleviate or completely eliminate symptoms of menopause. The therapeutic effect of Klimadynon® occurs gradually and becomes apparent after approximately two weeks of treatment.
Indications of Klimadinon Bionorica
Klimadinon is indicated for the relief of menopausal symptoms such as hot flashes and increased sweating.
Contraindications
Hypersensitivity to any of the drug’s components, lactose intolerance. Do not use in patients with estrogen-dependent tumors. Use with caution in patients with liver disease, epilepsy, and brain injury (use only after consultation with a physician).
How to take, dosage, and course of administration of Klimadinon Bionorica
Orally, 1 tablet twice daily at the same time (morning and evening). Swallow the tablets whole with a small amount of water. The duration of treatment is determined by a doctor.
Interactions
Interactions with other medications are currently unknown.
Special instructions
This medication should not be used for more than 3 months without consulting a doctor. If pregnancy occurs, discontinue use and consult a doctor. When used at recommended doses, this medication does not affect the ability to drive or operate machinery that requires increased alertness. Instructions for diabetics: Diabetics can take Klimadinon tablets, as a single dose contains less than 0.04 “bread units.”
Storage Instructions
Store in a dry, dark place at a temperature not exceeding 25°C. Keep out of reach of children.
Lisoprim Lor Lysozyme Pyridoxine
5,99 $Lisoprim Lor Lysozyme Pyridoxine Vitamin B6 Inulin 50 tab
Lisoprim Lor (Lysozyme Pyridoxine Inulin) has main component lysozyme, an antibacterial enzyme designed to protect against infectious pathogens. Lysozyme has the ability to destroy the structural basis of microorganism cells, neutralizing the cause of inflammation and sore throat: pathogenic bacteria and fungi.
Vitamin B6 (pyridoxine) has a protective effect on the oral mucosa.
Inulin is a prebiotic. When taken regularly as a supplement, inulin has a beneficial effect on the body, strengthens the immune system, and promotes the absorption of beneficial minerals.
Indications for Use Lisoprim Lor Lysozyme Pyridoxine Vitamin B6 Inulin
Recommended as a source of soluble dietary fiber – inulin, vitamin B6, which contains lysozyme.
Directions for Use
Adults: Take 2 tablets 5 times daily after meals. Dissolve slowly until completely dissolved. Do not chew or drink. Duration of treatment: 8-10 days. Repeat treatment if necessary.
Composition of Lisoprim Lor
Composition per tablet: inulin, lysozyme hydrochloride, magnesium stearate (anti-caking agent), pyridoxine hydrochloride (vitamin B6).
Active ingredients of Lisoprim Lor
Lysozyme
Lysozyme is an antibacterial enzyme that acts as a defense against infectious agents. It is present in leukocytes, mucous membranes, breast milk, tears, skin, and is especially abundant in saliva. Also Lysozyme has the ability to destroy the structural basis of microorganism cells, neutralizing the cause of inflammation and sore throat: pathogenic bacteria and fungi. Lysozyme hydrochloride is effectively used in ENT practice and dentistry in combination with other substances to treat laryngitis, sinusitis, pharyngitis, aphthous stomatitis, chronic septic conditions, purulent processes, frostbite, burns, conjunctivitis, corneal erosions, and other infectious diseases. Lysozyme acts as an antimicrobial agent, forcing the bacterial wall to rupture under its own internal pressure. It is also effective in destroying yeast cell walls. It has immunomodulatory, liquefying, and anti-inflammatory properties. Our bodies constantly produce lysozyme, but factors such as chronic infections, low stomach acid, antibiotic use, nutrient deficiencies, smoking, overwork, hypothermia, and poor environmental conditions deplete these reserves and reduce the body’s ability to produce new enzymes and protect itself. Furthermore, as we age, our bodies produce fewer enzymes, so they may require additional lysozyme.
Vitamin B6 (pyridoxine)
Vitamin B6 (pyridoxine) has a protective effect on the oral mucosa, is involved in almost all metabolic processes in the body, and also is effective against almost all types of intestinal diseases caused by impaired absorption, thereby supporting a healthy immune system.
Inulin
Another component of Lisoprim Lor, inulin, is an organic substance from the group of complex carbohydrates and polysaccharides obtained from processing the roots and tubers of certain plants. It belongs to the group of dietary fiber. Inulin is not digested in the upper digestive tract and reaches the intestines virtually unchanged, becoming food for the bifidobacteria present there, which then actively multiply. Inulin is a prebiotic that provides protection against dysbiosis and pathogenic bacteria. When consumed regularly as a supplement, inulin has a beneficial effect on the body, cleansing it, strengthening the immune system, promoting the absorption of beneficial minerals, and normalizing digestion and metabolism.
Daily Dose
Content per 10 tablets:
Vitamin B6, 5.0 mg
Inulin, 1600 mg
Lysozyme, 200 mg
Contraindications
Individual intolerance to any of the ingredients, pregnancy, or breastfeeding.
Consult a physician before use.
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Mastodinone Bionorica
19,99 $Mastodinone Bionorica 60 tablets
Manufacturer of Mastodinone Bionorica: Bionorica SE. Kerschensteinerstrasse 11-15, 92318 Neumarkt, Germany
Composition of Mastodinone Bionorica
1 tablet contains:
Active ingredients:
Vitex agnus castus (Agnus castus) Ø 162.0 mg
Caulophyllum thalictroides D4 81.0 mg
Cyclamen europaeum (Cyclamen) D4 81.0 mg
Strychnos ignatii (Ignatia) D6 81.0 mg
Iris versicolor (Iris) D2 162.0 mg
Lilium lancifolium (Lilium tigrinum) D3 81.0 mg
Excipients: potato starch, magnesium stearate, lactose monohydrate.
Indications of Mastodinone Bionorica
As a symptomatic treatment, as recommended by a physician, in combination therapy for:
– premenstrual syndrome, accompanied by mastodynia, breast tenderness, mental instability, constipation, edema, headache/migraine;
– fibrocystic breast disease;
– menstrual irregularities and/or infertility caused by corpus luteum insufficiency.
Contraindications
Hypersensitivity to any of the components of the drug.
Pregnancy and breastfeeding.
Age under 12 years.
Lactose intolerance, lactase deficiency, or glucose-galactose malabsorption syndrome (the drug contains lactose).
Use during pregnancy and breastfeeding
During pregnancy, the indications for taking Mastodynon automatically disappear.
Data obtained from reproductive toxicity studies confirm that Vitex agnus castus affects milk production. This product is not recommended for use during breastfeeding.
Side effects
Severe allergic reactions with facial swelling, shortness of breath, and dysphagia are possible. Skin allergic reactions (skin rash, urticaria), gastrointestinal disturbances (nausea, epigastric pain), headache, dizziness, acne, and menstrual irregularities may also occur. The frequency of adverse reactions is unknown (cannot be estimated from the available data). If the above-mentioned adverse reactions or any other adverse reactions not listed in the instructions occur, discontinue use and consult a doctor.
How to take, dosage, and course of administration of Mastodinone Bionorica
Take 1 tablet orally twice daily with a small amount of liquid.
To achieve the optimal therapeutic effect, it is recommended to continue taking Mastodynon® for 3 months (including during menstruation).
If symptoms persist after 3 months of taking Mastodynon, consult a doctor.
Interactions
The drug’s effectiveness may be reduced when taken concomitantly with dopamine receptor antagonists, and interactions with dopamine receptor agonists, estrogens, and antiestrogens are also possible. If you are using any of the above or other medications (including over-the-counter medications), consult a doctor before using Mastodynon.
Overdose
Gastrointestinal disturbances may occur in patients with lactose intolerance. In case of overdose, treat symptomatically.
Special Instructions
Mastodynon should be used as directed and under the supervision of a physician.
Patients taking dopamine receptor agonists, dopamine receptor antagonists, estrogens, or antiestrogens should consult a physician before using Mastodynon.
If symptoms worsen while taking the drug, consult a physician.
Patients with a history of estrogen-dependent malignancies or pituitary disease should consult a physician before using the drug.
The drug promotes gradual normalization of hormonal balance, which may cause menstrual irregularities.
If pregnancy occurs while taking Mastodynon, discontinue use.
There is insufficient data on the use of the drug in children under 12 years of age. Mastodynon® should not be used in children aged 12 years or older until the onset of regular menstruation during puberty.
Taking homeopathic medicines may temporarily worsen existing symptoms (primary aggravation). In this case, discontinue use and consult a doctor.
Smoking, stimulants, coffee, and alcohol consumption negatively impact the effectiveness of homeopathic medicines. For patients with diabetes: 1 tablet of Mastodinon contains approximately 0.02 “bread units.”
This medicine does not contain gloten.
Storage conditions
Store in a dry, dark place, at a temperature not exceeding 25°C. Keep out of reach of children.
Mastodinone Bionorica 60 tablets feedbacks
Please take a look at another product from our store with similar properties:
Meloxicam for Pets 0.5 mg 10 tablets
13,99 $Meloxicam for Pets 0.5 mg 10 tablets
Meloxicam for Pets 0.5 mg nonsteroidal anti-inflammatory remedy suitable for dogs and cats, pack of 10 tablets
Quickly and effectively relieves pain and inflammation.
>Two tablet dosages for convenient administration and dosage adjustment, for adult animals, as well as for puppies and kittens over 6 weeks old.
>If your pet’s condition is chronic, you can use this product long-term.
Ingredients
Meloxicam content per tablet: 0.5 mg. The excipients include microcrystalline cellulose, sodium starch glycolate (type A), colloidal silicon dioxide, aspasvit C 200, talc, calcium stearate, and lactose monohydrate.
Indications
Meloxicam is used as an anti-inflammatory, antipyretic, and analgesic agent for inflammatory and pain syndromes of various origins in dogs and cats, including acute and chronic diseases of the musculoskeletal system: arthritis, arthrosis, synovitis, dislocations, inflammatory diseases of soft tissues, as well as the postoperative period. Meloxicam is not intended for use in pregnant and lactating females, puppies and kittens under 6 weeks of age.
How to use it
For dogs and cats, orally, forcefully onto the root of the tongue once a day, during feeding.
Dogs:
Day 1 of treatment: 2 tablets per 5 kg of body weight (0.2 mg meloxicam per 1 kg of body weight).
Days 2 and subsequent: 1 tablet per 5 kg of body weight (0.1 mg meloxicam per 1 kg of body weight).
Cats:
Day 1 of treatment: 1 tablet per 5 kg of body weight
Days 2 and subsequent: 0.1 mg meloxicam per 1 kg of body weight.
*For cats, the treatment course should not exceed 4 days.
Only the specific diagnosis and the severity of clinical symptoms determine the duration of treatment. In acute cases, treatment lasts 5-7 days. In some chronic cases, treatment may last up to 28 days under veterinary supervision.
Storage conditions:
Store the product in the original packaging, protected from direct sunlight. And also separate from food and feed, at a temperature of 2°C to 25°C.
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Methyluracil Ointment 10%
6,99 $Methyluracil Ointment 10% 25g
Composition of Methyluracil Ointment
100g of ointment contains:
Active ingredient:
Dioxomethyltetrahydropyrimidine (methyluracil) 10.0g
Excipients:
Vaseline 45.0g
Anhydrous lanolin 31.5g
Purified water 13.5g
Pharmacological action
Pharmacotherapeutic group: Tissue repair stimulant
Pharmacological properties
Possesses anabolic activity. By normalizing nucleic acid metabolism, it accelerates cellular regeneration processes in wounds, promoting tissue growth, granulation maturation, and epithelialization.
When applied topically, it has photoprotective properties.
Indications of Methyluracil Ointment
As part of combination therapy for poorly healing wounds, burns, and photodermatitis. Prevention of skin reactions to irradiation of neoplasms with low radiosensitivity, reduction of symptoms of radiation dermatitis, and late vaginal wall adhesions (occlusions) in cases of radiation therapy for genital neoplasms.
Use during pregnancy and breastfeeding
The drug may only be used if the expected benefit to the mother outweighs the potential risk to the fetus and child. If the drug must be prescribed during lactation, breastfeeding should be discontinued.
Contraindications
Hypersensitivity to any of the drug’s components, excessive granulation.
Use with caution
Pregnancy, breastfeeding, children under 3 years of age.
Side effects
Allergic reactions such as itching, hyperemia, and a short-term burning sensation at the application site.
Interactions
The drug is compatible with topical antibacterial and antiseptic agents.
Directions for use, course of administration, and dosage
External and local application.
Apply a thin layer of 5-10 g of ointment to the affected areas daily for 15-30 days. Before application, the wound should be treated with an antiseptic and any remaining necrotic tissue should be removed.
In cases of radiation therapy for genital tumors, the ointment is used in loose tampons for the prevention and treatment of radioepitheliitis.
Storage conditions
At a temperature not exceeding 25°C.
Keep out of reach of children.
Shelf life
3.5 years. Do not use after the expiration date.
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Miramistin Solution 150ml
14,99 $Miramistin Solution for External Use 0.01% 150ml
Miramistin solution is used in various fields, including:
Otolaryngology
Comprehensive treatment of acute and chronic otitis, sinusitis, tonsillitis, laryngitis, and pharyngitis. In children aged 3 to 14 years – for the comprehensive treatment of acute pharyngitis and/or exacerbation of chronic tonsillitis.
Dentistry
Treatment and prevention of infectious and inflammatory diseases of the oral cavity: stomatitis, gingivitis, periodontitis, and periodontitis. Hygienic treatment of removable dentures.
Surgery and traumatology
Prevention of suppuration and treatment of purulent wounds, treatment of purulent-inflammatory processes in the musculoskeletal system.
Obstetrics and gynecology
Prevention and treatment of suppuration from postpartum injuries, perineal and vaginal wounds, postpartum infections, and inflammatory diseases (vulvovaginitis, endometritis). Combustiology — treatment of superficial and deep second- and third-degree burns, preparation of burn wounds for dermatoplasty.
Dermatology
Treatment and prevention of pyoderma and dermatomycosis, candidiasis of the skin and mucous membranes, and athlete’s foot.
Venereology
Individualized prevention of sexually transmitted diseases (syphilis, gonorrhea, chlamydia, trichomoniasis, genital herpes, genital candidiasis).
Urology
Comprehensive treatment of acute and chronic urethritis and urethroprostatitis of specific (chlamydia, trichomoniasis, gonorrhea) and non-specific etiologies.
Composition
Per 1 liter:
benzyldimethyl [3-(myristoylamino)propyl] ammonium chloride monohydrate (calculated as anhydrous substance) 0.1 g
Excipient: purified water – up to 1 liter
Directions for use and dosage Miramistin solution
Topical. The product is ready for use.
Instructions for use with the spray nozzle.
1. Remove the cap from the bottle; for the 50 ml bottle, also remove the urological applicator.
2. Remove the included spray nozzle from its protective packaging.
3. Attach the spray nozzle to the bottle.
4. Activate the spray nozzle by pressing it again.
Instructions for use with the 50 or 100 ml bottle with the gynecological nozzle.
1. Remove the cap from the bottle.
2. Remove the included gynecological nozzle from its protective packaging.
3. Attach the gynecological nozzle to the bottle without removing the urological applicator.
Surgery, Traumatology, Combustiology
For preventive and therapeutic purposes, irrigate the surface of wounds and burns, loosely pack wounds and fistula tracts, and secure gauze pads soaked in the preparation. Repeat the treatment procedure 2-3 times a day for 3-5 days. Active drainage of wounds and cavities with a daily application rate of up to 1 liter of the preparation is highly effective.
Obstetrics, Gynecology
For the prevention of postpartum infection, 50 ml of the preparation is applied as a tampon before delivery (5-7 days), after each vaginal examination during delivery, and in the postpartum period, leaving it in place for 2 hours for 5 days. Use the gynecological nozzle included in the kit for easy irrigation of the vagina. For women delivering by cesarean section, the vagina is treated immediately before the surgery, the uterine cavity and incision are treated during the surgery, and tampons soaked in the preparation are inserted into the vagina for 2 hours for 7 days postoperatively. Treatment of inflammatory diseases lasts for a 2-week course by intravaginal injection of tampons soaked in the drug, as well as by drug electrophoresis.
Venereology
For the prevention of sexually transmitted diseases, the preparation is effective if used no later than 2 hours after intercourse. Using a urological applicator, insert the contents of the vial into the urethra for 2-3 minutes: 2-3 ml for men, 1-2 ml for women, and 5-10 ml into the vagina. For convenience, use a gynecological nozzle. Treat the skin of the inner thighs, pubis, and genitals. After the procedure, it is recommended not to urinate for 2 hours.
Urology
For the combined treatment of urethritis and urethroprostatitis, 2–3 ml of Miramistin solution is injected into the urethra 1–2 times daily for 10 days.
Otolaryngology
For purulent sinusitis, the maxillary sinus is rinsed with a sufficient amount of the drug during the puncture.
Tonsillitis, pharyngitis, and laryngitis are treated by gargling and/or irrigation with a spray nozzle, pressing 3–4 times 3–4 times daily. The amount of drug per gargle is 10–15 ml.
Children
In case of acute pharyngitis and/or exacerbation of chronic tonsillitis, spray the child‘s throat with a spray nozzle. Children aged 3–6 years: 3–5 ml per spray (press the spray head once) 3–4 times daily; 7–14 years: 5–7 ml per spray (press twice) 3–4 times daily; 14 years and older: 10–15 ml per spray (press 3–4 times) 3–4 times daily. Duration of therapy ranges from 4 to 10 days, depending on the onset of remission.
Dentistry
For stomatitis, gingivitis, and also for periodontitis, rinse your mouth with 10-15 ml of the drug 3-4 times a day.
Storage conditions
At room temperature.
Expiration date
3 years old
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Miramistin Suppositories 10 pcs
9,99 $Miramistin Vaginal Suppositories 15 mg 10 pcs
The drug Miramistin in the form of vaginal suppositories is an antiseptic for local use in gynecology.
Miramistin Suppositories has a broad spectrum of antimicrobial activity, including hospital strains resistant to antibiotics.
Per 15 mg suppository:
Active ingredient: benzyldimethyl[3-(myristoylamino)propyl]ammonium chloride monohydrate (calculated as anhydrous) – 15 mg.
Excipients: macrogol 400 (polyethylene glycol 400) – 114.2 mg; macrogol 1500 (polyethylene glycol 1500) – up to a suppository weight of 2300 mg.
Miramistin Suppositories Indications
Prevention and treatment of inflammatory diseases in gynecology (vulvovaginitis, bacterial vaginosis);
Prevention and treatment of suppuration from postpartum injuries, vaginal wounds, and postpartum infections.
Dosage and Administration
Intravaginal.
Before use, remove the suppository from its liner.
Prescribe one 10 mg suppository twice daily (at 12-hour intervals) or one 15 mg suppository once daily (at 24-hour intervals) for 7 days.
Insert the suppository as deeply as possible into the vagina; do not use soap or other soap-based products to clean the genital area for 2 hours before and 2 hours after intravaginal administration of Miramistin® (use only clean water).
If improvement does not occur after treatment, or symptoms worsen, or new symptoms appear, consult a doctor. It is recommended to use the drug only as directed and in the doses specified in the instructions.
Use during pregnancy and breastfeeding
According to available data, use of the drug during pregnancy and breastfeeding is possible, as the drug does not have a systemic effect when used according to the instructions.
Consult a doctor before using the drug during pregnancy, if you suspect pregnancy, or if you are planning a pregnancy.
If you are pregnant, think you might be pregnant, or are planning a pregnancy, consult a doctor before using the drug.
Consult a doctor before using the drug during breastfeeding.
Miramistin Suppositories Contraindications
Hypersensitivity to the active substance or components of the drug;
Children under 18 years of age.
Storage Instructions
Store Miramistin Suppositories out of the reach of children at a temperature not exceeding 25°C.
Miramistin Vaginal Suppositories 15 mg 10 pcs feedbacks
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Ointment Vishnevsky Balsamic Liniment
3,99 $Ointment Vishnevsky Balsamic Liniment 30g
Ointment Vishnevsky Balsamic Liniment is a combination product for external use. It has an antiseptic and local irritant effect, accelerating regeneration processes.
Birch tar has keratoplastic, antiseptic, anti-inflammatory, and local irritant properties, and helps improve tissue blood flow.
Bismuth tribromophenolate and bismuth oxide complex (xeroform) has astringent, adsorbent, anti-inflammatory, and also antiseptic properties. When applied topically, xeroform accelerates tissue regeneration.
Active ingredients
Birch Tar + bismuth tribromophenolate and bismuth oxide complex
Composition
Liniment 1 g, tar 30 mg, xeroform 30 mg.
Indications
—Skin abscess;— Furuncle;— Lymphangitis;— Burns;— Frostbite;— Wounds;— Ulcers;— Bedsores.
Directions for use of Ointment Vishnevsky Balsamic Liniment
Topical.
>Apply a thin layer of the preparation to the affected area or apply a gauze bandage soaked in the liniment.
>If no improvement occurs after treatment, or if symptoms worsen, or if new symptoms appear, consult a doctor.
Use the preparation only as directed and in the dosages specified in the instructions. If necessary, consult a doctor before using the medication.
Contraindications
— Hypersensitivity
Special instructions
Avoid contact with mucous membranes or eyes. After applying the product, wash your hands thoroughly to prevent contact with your eyes, mouth, or nose. If eye contact occurs, rinse with water. Wash hands thoroughly after applying liniment to prevent contact with eyes, nose, and mouth. Not recommended for use by individuals with hypersensitivity to phenol and its derivatives. The liniment has a distinctive odor and may stain clothing. Birch tar, which is part of the liniment, can increase sensitivity to sunlight, so in the summer you should avoid exposure to the sun during treatment with the drug.
Description of Ointment Vishnevsky Balsamic Liniment
Liniment, light yellow to dark brown in color, with a distinctive odor.
Storage temperature
2℃ to 25℃
Shelf life is 5 years.
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Quartz Ultraviolet Irradiator Solnyshko
79,99 $Solnyshko Quartz Ultraviolet Irradiator OUFK-01M Rhinitis Bronchitis Asthma
The OUFk-01M Quartz Ultraviolet Irradiator Solnyshko is intended for general and intracavitary local irradiation of inflammatory diseases in otolaryngology in medical, medical and preventive care, health resorts, and at home.
INDICATIONS of Solnyshko Quartz Ultraviolet Irradiator OUFK-01M
Influenza, acute respiratory viral infections and their complications (acute tubootitis, acute laryngotracheitis, tonsillitis, acute inflammation of the maxillary sinuses (sinusitis), etc.).
Diseases of the mucous membranes of the throat and nose.
Vasomotor rhinitis, acute chronic rhinitis.
Diseases of the external auditory canal.
Acute periodontitis, chronic periodontosis, stomatitis, post-extraction infiltrates, and gum inflammation.
Purulent wounds, trophic ulcers.
Clean wounds.
Bronchitis. Bronchial asthma.
Bone fractures.
Postoperative ultraviolet irradiation.
CONTRAINDICATIONS
Malignant neoplasms at any stage.
Diseases, including those following radical surgery.
Systemic connective tissue diseases.
Active pulmonary tuberculosis.
Hyperthyroidism.
Fevers.
Tendency to bleeding.
Circulatory failure grades II and III.
Arterial hypertension grade III.
Severe atherosclerosis.
Myocardial infarction (first 2-3 weeks).
Acute cerebrovascular accident.
Kidney and liver disease with insufficiency.
Peptic ulcer disease during an exacerbation.
Chronic hepatitis, pancreatitis with signs of active process.
Cachexia.
Increased sensitivity to UV rays, photodermatoses.
MAIN CHARACTERISTICS of Solnyshko Quartz Ultraviolet Irradiator OUFK-01M
DKBU-7 lamp.
Effective radiation range: 180-275 nm (shortwave).
Power consumption: no more than 300 VA.
The device’s operating mode warm-up time is no more than 1 minute from the moment the irradiator lamp lights up.
The device provides 8 hours of operation per day in a cyclic mode: 10 minutes on, 15 minutes off.
Overall dimensions of the irradiator: no more than 275 x 145 x 140 mm.
Weight of the set: no more than 1 kg.
Power supply: 220 V, frequency: 50 Hz.
PACKAGE CONTENTS
- Ultrasound quartz irradiator, OUFk-01M “Solnyshko” version – 1 pc.
- UV protective goggles – 1 pc.
- Tube with a 5 mm diameter outlet – 1 pc.
- Tube with a 15 mm diameter outlet – 1 pc.
- Tube with a 60° outlet – 1 pc.
- Biodosimeter – 1 pc.
- Shutter – 1 pc.
- Operation manual.
- Instructions for use.
Sinupret Bionorica
19,99 $Sinupret Bionorica 50 tab
Sinupret Bionorica Manufacturer:
Bionorica SE, Germany
Ingredients of Sinupret Bionorica
Active ingredients: Gentian root – 6.0 mg; Primrose flower – 18.0 mg; Sorrel herb – 18.0 mg; Elder flower – 18.0 mg; Verbena herb – 18.0 mg. Excipients: Gelatin, lactose monohydrate, potato starch, colloidal silicon dioxide anhydrous, sorbitol, stearic acid. Tablet shell: Basic butyl methacrylate copolymer, calcium carbonate, castor oil, chlorophyll powder, dextrin, glucose, indigo carmine aluminum lake (E 132), magnesium oxide, corn starch, montan glycol wax, riboflavin (E 101), shellac, sucrose, talc, titanium dioxide.
Pharmacological action
A combination drug of herbal origin. Sinupret has secretolytic, secretomotor, anti-inflammatory, decongestant, moderate antibacterial, and also antiviral effects. It promotes the drainage of exudate from the paranasal sinuses and upper respiratory tract, and as a result, preventing the development of complications.
Indications of Sinupret Bionorica
Acute and chronic sinusitis accompanied by the formation of viscous secretions.
Contraindications
Hypersensitivity to any of the drug’s components, lactase deficiency, glucose-galactose malabsorption, sucrase/isomaltase deficiency, lactose, fructose, or galactose intolerance (due to the drug’s content of lactose monohydrate, glucose, and sucrose); children under 6 years of age (due to insufficient clinical data).
Side effects
Allergic reactions (skin rash, redness, itching, angioedema, shortness of breath), and gastrointestinal disturbances (epigastric pain, nausea) may occur. If side effects occur, discontinue use and consult a doctor.
How to take, dosage, and course of administration of Sinupret Bionorica
Orally, without chewing, with a small amount of water. Adults: 2 tablets 3 times daily. School-age children: 1 tablet 3 times daily. The course of treatment is 7-14 days. If symptoms persist for more than 7-14 days or recur periodically, consult a doctor.
Overdose
In case of overdose, the severity of dose-dependent side effects may increase.
Special instructions
Use of this medication does not affect the ability to perform potentially hazardous activities requiring increased concentration and psychomotor skills (including driving and operating moving machinery). Instructions for patients with diabetes: The digestible carbohydrates contained in one tablet are approximately 0.01 “bread units” (BU).
Storage Instructions
Store in a dry, dark place at a temperature not exceeding 25°C. Keep out of reach of children.
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Mastodinone Bionorica 60 tablets
Soviet Baby Cream Svoboda 40g
4,99 $Soviet Baby Cream Svoboda 40g
Soviet Baby Cream Svoboda is a classic baby cream: provides excellent skin protection, preventing irritation and redness; promotes healing of cracks and other skin conditions; and is used as a preventative measure against chapping and diaper rash. This baby cream is also a universal product that can be used at any age, starting from birth, as it is suitable even for particularly sensitive skin! Classic Baby Cream offers a solution to a wide range of skin problems and minimizes allergic reactions!
Clinically tested.
This time-tested cream with a pleasant scent provides a gentle effect and a familiar scent. Suitable for both children and adults with problematic, dry skin.
Directions for use and dosage
Apply the desired amount of cream to clean skin and massage in gently until completely absorbed. Additionally, apply cream for bottom hydration.
How this cream works
It provides a mild cooling effect, providing relief for children with irritated skin. The cream is fragrance-free.
Pharmacological action Soviet Baby Cream Svoboda
This cream is an essential cosmetic product for caring for the delicate and sensitive skin of babies. It contains a complex of natural ingredients: lanolin, chamomile extract, lavender oil, menthol, and vitamin A. The cream nourishes, softens, and protects babies’ skin from irritation and diaper rash. It has a mild cooling effect, relieving the condition of children with irritated skin. The cream is perfume-free. Special features: 1. For sensitive skin 2. Hypoallergenic 3. Chamomile extract has a soothing effect on sensitive baby skin 4. Natural oils and lanolin soften and restore the skin 5. Has a mild cooling effect 6. Does not contain perfume. Result: The cream nourishes, softens, and protects babies’ skin from irritation and diaper rash.
Ingredients
Water, mineral oil, ceresin, paraffin, polyglyceryl-2 sesquiisostearate, shortening, lanolin, PEG-45/dodecyl glycol copolymer, retinyl palmitate (vitamin A), chamomile flower extract, lavender oil, menthol, benzyl acetate, benzyl alcohol.
Storage conditions
T=+(05-25)C
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Spasatel Balm
5,99 $Spasatel Balm 30g
The original Spasatel balm is your first aid for superficial wounds, burns, sprains. Spasatel Balm contains a complex of substances that exhibit a synergistic effect. Milk lipids have nourishing, regenerating, and softening properties. They form a film on the skin’s surface, reduce moisture evaporation, prevent the skin from drying out, and also promote the normal natural regeneration process of damaged tissue.
Indications of Spasatel Balm
“Spasatel” balm is intended for rapid relief of: superficial and deep wounds; purulent processes in fresh wounds; first- to third-degree burns; acute inflammatory processes on the skin and mucous membranes; various superficial skin injuries; irritations, diaper rash; protection from chapping, sun, and frost; accelerated healing of bruises, hematomas, and abrasions; relief from sprains;
Ingredients
Ghee, capsaicin oil solution, fir essential oil, olive oil, purified turpentine oil, sea buckthorn oil, oil extracts of Rhodiola rosea, calendula, and eleutherococcus, methyl nicotinate, vitamin E, vitamin A, methylparaben, and propylparaben. Only natural products without the use of hormonal or antibiotic agents.
How the ingredients of the Spasatel balm work
“Spasatel” consists of natural ingredients with protective and healing properties. It does not contain chemical fragrances or dyes. Clarified butter retains the active ingredients of the cream on the skin. The fat base allows the balm to be used at subzero temperatures, protecting the baby’s skin from frost and chapping during walks.
How the oils in the composition of the Spasatel balm work
Refined Naftalan oil is mined only in the area around the town of Naftalan and has long been used for medicinal purposes: it has antiseptic, absorbent, and analgesic properties, and is indicated for dermatitis and eczema. Calendula oil extract soothes the skin, has an anti-inflammatory effect, and prevents redness, flaking, and irritation. Vitamins A and E accelerate skin regeneration and renewal, supporting the skin’s protective functions and healing skin damaged by adverse environmental factors (burns, including sunburn, chapping). Beeswax has a restorative effect on the skin. Tea tree essential oil has antibacterial, antifungal, and anti-inflammatory properties, protecting skin with a damaged protective layer from infection without the negative side effects of synthetic products. Lavender essential oil refreshes and cools the skin, has an anti-edematous and detoxifying effect, and eliminates irritation and flaking. Olive and sea buckthorn oils have restorative and softening effects, and possess wound-healing and disinfectant properties.
Pharmacological action
Use this balm for rapid relief of various traumatic injuries and acute skin inflammations; irritations; diaper rash; protection from chapping, sun, and frost. Spasatel Balm promotes accelerated healing of fresh wounds and burns without scarring. The absorbent action of the balm allows a person to return to work in less than 24 hours after sprains, severe bruises, and superficial hematomas. The balm’s unique mechanism of action is based on its ability to restore the protective properties of damaged skin and initiate regenerative processes. This dramatically accelerates healing, preventing the formation of scars, infections, and intoxications. Its powerful bacteriostatic effect is due to the regulation of biochemical processes in tissues and is accompanied by the activation of the bactericidal properties of blood and lymphatic elements, resulting in rapid wound healing. The balm quickly reduces pain not through direct anesthetic action, but by restoring balance in affected tissues.
Directions, course of treatment, and dosage
Apply the balm generously to the affected area and, if necessary, cover with a bandage with an insulating layer to prevent absorption of the balm. If the nature of the skin injury allows, apply with gentle massage movements and rub in gently. Reapply the balm when your skin has absorbed it. Healing time depends on the size of the injured area and the urgency of the initial application. The clinical healing effect appears several hours after applying the bandage. If necessary, apply the balm several times until you feel comfortable.
Results
This product will quickly and scarlessly relieve any fresh wounds, burns, frostbite, bruises, suppurations, and inflammation.
Action
Spasatel has the following pharmacological properties: regenerative, antibacterial, soothing, healing, moisturizing, protective, detoxifying, analgesic, and absorbable. The balm stimulates wound cleansing and the natural restoration of damaged dermal layers. Its analgesic effect is achieved by inhibiting the synthesis of inflammatory mediators and reducing their impact on tissue. It does not irritate the skin upon application, making it suitable for pediatric use. The clinical effect is rapid, and the therapeutic response is evident within a few hours.
Storage Conditions
Store in a dry place at a temperature not below 5°C and not above 25°C.
Spasatel Balm 30g feedbacks
Please take a look at another product from our store with similar properties: Eplan Cream 30g
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