The instruction for medical use
of HLOROFILLIPT medicine
the Trade name
the International unlicensed name
Is not present
the Dosage form
Solution of alcohol 10 mg/ml
1 ml of solution contains
active agent – the chlorofillipt extract dense (in terms of 100% content of dry matter) 10 mg,
excipients – alcohol of 96%
Transparent liquid of green color
of Antiseptics and disinfecting drugs other
the ATX D08A X Code
Drug properties contains mix of the chlorophyll which is in eucalyptus leaves. Has antibacterial and anti-inflammatory activity, stimulates the immune system, has anti-hypoxemic effect. At topical administration promotes regeneration of the damaged fabrics, shows detoksikatsionny properties. Does not render cancerogenic, mutagen, teratogenic and embriotoksichesky effects.
of the Disease caused by antibiotic-resistant stafilokokka
– burns, trophic ulcers, erosion of a neck of the uterus
– inflammatory diseases of lungs, ENT organs
– infectious diseases of digestive tract
– inflammatory diseases of the parodont, bacterial damages of a mucous membrane of an oral cavity
the Route of administration and doses
appoint Drug inside, rektalno and locally.
Inside appoint the adult on 5 ml 1% of alcohol solution of the drug divorced in 30 ml of water, 25 drops 3 times a day in 40 minutes prior to food daily. Course of treatment of 7-10 days.
Rektalno is applied in the form of enemas: 20 ml of 1% of alcohol solution part in 1 l of water (a dose for 1 enema). With chlorofillipty give an enema every 2 day. The course of treatment consists of 10 procedures.
For topical administration (treatment of burns and trophic ulcers) 1% alcohol solution part 1:5 0.25% with novocaine solution. In an erosion of a neck of the uterus apply 1% alcohol solution (greasing of the canal of a neck of the uterus and an erosion, wetting of the tampons entered into a vagina).
– puffiness of lips, a mucous membrane of a nasal cavity, pharynx
– skin rashes, an itching
– individual intolerance of drug
– the children’s age up to 18 years
Exponentiates effect of antiseptic drugs and antibiotics. Drug contains 96% alcohol therefore at simultaneous use strengthening of effects of psychotropic, myorelaxation drugs and alcohol is possible. It is necessary to consider what in the presence in a wound of residues of peroxide of hydrogen chlorofillipt drops out in a deposit therefore after bathing of the wound by hydrogen peroxide its remains have to be removed with sterile isotonic solution of sodium chloride.
Irrespective of the chosen route of administration, before an initiation of treatment define sensitivity to a chlorofillipt for what the patient drinks 25 drops of the drug dissolved in 1 tablespoon of water. At absence in 6-8 hours of symptoms of an allergy (puffiness of lips, mucous a pharynx, etc.) it is possible to use drug.
Drug contains 96% alcohol therefore patients should not appoint it in the presence at them tendency ment of dependence on alcohol or drugs and also patients with the profound abnormal liver function, epilepsy, diabetes.
Pregnancy and the period of a lactation
during pregnancy and in the period of a lactation the use of drug is possible if the expected advantage exceeds risk for a fruit and mother.
The feature of influence of medicine on ability to run the vehicle or potentially dangerous mechanisms
during treatment should abstain from potentially dangerous types of activity requiring special attention as drug contains alcohol.
Symptoms – strengthening of side effects is possible.
Treatment is symptomatic.
Form of release and packing
On 100 ml in the bottles from dark brown opaque polymer with a screw mouth with a capacity of 125 ml corked by covers with control of the first opening. On a bottle paste the self-adhesive label.
Each bottle together with the instruction for medical use in the state and Russian languages is placed in a pack from cardboard.
To Store storage conditions in the place protected from light at a temperature from 15 ºС up to 25 ºС.
To store out of children’s reach!
Not to apply a period of storage of 5 years after the expiration date specified on packing.
According to the prescription
LLC GNCLS Experimental Plant Producer.
Ukraine, Kharkiv, Vorobyov St., 8.
The owner of the registration certificate
of LLC GNCLS Experimental Plant, Ukraine
the Address of the organization accepting in the territory of the Republic of Kazakhstan claims from consumers on quality of products (goods) the Address: LLC GNCLS Experimental Plant. Ukraine, Kharkiv, Vorobyov St., 8. Phone: 752-30-17Факс: 752-30-17Электронный address: email@example.com
the Authorized representative in the territory of the Republic of KazahstanAdres: KFK Medservice Plus LLP 050004, Republic of Kazakhstan, Almaty, Mametova St., 54 Phone number / fax: (727) 279 98 21 E-mail address: firstname.lastname@example.org