You have been prescribed this medicine if you have any of the following:
You should consult your doctor if you experience any of the following:
Usually the preparation is well tolerated. During a long-term usage of high doses there can be possible follow side effects:
nausea, vomiting, heartburn, diarrhea.
hyperexcitability of CNS, headache.
formation of urinary, cystine and oxalate concernments.
Skin and subcutaneous tissue: allergic reactions.
It can cause erythrocyte hemolysis in patients with insufficiency of glucose-6-phosphatdehydrogenase of hematocytes.
If it is almost time for your next dose, skip the dose you missed and take your next dose when you are meant to. Otherwise take it as soon as you remember and then go back to taking it as you would normally.
Ascozin® increases salicylates (increases a risk of crystalluria), ethynilestradiol,
benzylpenicillin and tetracyclines concentrations in blood, and decreases per oral
contraceptives concentration in blood. It reduces anticoagulation effect of coumarin
derivatives. It improves iron drugs absorption in intestine. It increases general
clearance of ethyl alcohol. Quinolone drugs, calcium chloride, salicylate, corticosteroid
decrease vitamin C reserve when used for a long term. Corticosteroids (cortisone
and prednisolone), which are administered in concrete diseases (arthritis, bronchial
astma etc), also reduce vitamin C and zinc levels.
Concurrent usage of ascorbic acid and deferoxamine enhances tissue toxicity of iron, especially in cardiac muscle that can cause decompensation of blood circulatory system. It can be used only in 2 hours after deferoxamine injection. A long-term administration of high doses in patients, who are treated by disulfiram, inhibits disulfamide-alcohol reaction.
High doses of the preparation decrease efficacy of tricyclic depressants.
nausea, vomiting, intestine spasm, diarrhea; it is possible allergic reaction, kidney dysfunction, blood pressure increase, hyperexcitability of CNS, sleep disturbance.
It is symptomatic.
Tell your doctor immediately if you become pregnant while taking this medication. For safety of any drug during pregnancy or breastfeeding – please consult your doctor.
Store in a dry, protected from light place at a temperature not more than 25° C.
Keep it out of reach of children.
1 ml of cutaneous solution contains dimethicone 40 mg;
Pediculosis (for removing head lice and their eggs).
The use in children under 6 months requires medical supervision.
Adults and children (aged 6 months and above).
Apply a sufficient amount of solution on dry hair from the base to the tip so that the agent is distributed throughout the hairy part of the head. Distribute the liquid through the hair from roots to tips. Allow hair to dry naturally. Remov® should be left on hair for a minimum of 8 hours or overnight. Then wash your hair with regular shampoo, rinse thoroughly with water. Repeat the treatment in seven days.
Dimethicone is generally well tolerated. Minimal side effects include itching and flaky scalp and irritation/wetness around the eyes.
Pregnancy and lactation:
Consult a doctor in case of necessity of using the drug during pregnancy and lactation.
The drug Remov® can be applied in children since birth.
Stop the application with the appearance of skin rash or other signs of local or general hypersensitivity.
The drug is intended for external use only.
In case of accidental contact with eyes rinse them with water.
Do not inhale.
While Remov® is applied on hair, one should avoid contact with naked flames, cigarettes and other sources of ignition. Remov® is not water-based and can not prevent hair ignition.
Overdose syndromes are unknown.
Ability to influence reaction velocity while driving or operating any other mechanisms.
Hypersensitivity to any component of the drug.
Ectoparasiticides, also used against scabies.
АТС code P03A X05.
Remov® contains dimethicone, which is used in many pharmaceutical and cosmetic products. A 4% substance concentration has been found to affect the physico-physiological activity of lice. It is less effective in its ovicidal activity, therefore two applications 7 days apart are required.
The drug does not contain neurotoxic organophosphate insecticides, therefore it does not affect the specific enzymes of lice. Remov® has an effect on parasites by a physical
Tt covers the louse and disrupts the ability of its organism to maintain water balance, so that the treated insects fail to excrete surplus water. The drug activity is not diminished in insecticide-resistant head lice.
The preparation is applied topically on the affected surface, but its dermal absorption is insignificant or absent.
General physic-chemical properties:
Transparent, colorless, odorless homogeneous solution.
Store below 25°С in original package.
Keep it out of reach of children.
50 ml in a bottle, 1 bottle in a carton box.
50 ml in a bottle with a spray gun, 1 bottle in a carton box.
Conditions of supply.