Mardil zinc max
For external use
The treatment process is carried out on an outpatient basis under the supervision of a doctor. The procedure does not require anesthesia. The drug is applied with a plastic spatula, a cotton swab or using a glass capillary on the surface of the formation, previously degreased with 70% alcohol. Treatment is carried out 1-3 applications until a whitish-gray color appears. The color of the tissue changes within 2-3 minutes after application of the drug. In the presence of severe hyperkeratosis, within 5-7 minutes. At the same time, the consistency of the neoplasm changes to a denser one. The dosage of the drug depends on the type, size, density and severity of hyperkeratosis and can be 0.02 ml-0.2 ml. The maximum daily dose is 0.2 ml.
The number of treatment sessions varies from 1 (flat warts) to 3-4 (plantar warts) until the element completely disappears with an interval between sessions of at least 24 hours. A transient strip of hyperemia and edema is observed around the neoplasm after application of the drug Mardil Zinc® Max , which disappears without a trace 25-40 minutes after completion of the procedure. No additional therapeutic measures are required after application of the drug. The next day after application, the pathological lesion mummifies, acquires a dark brown tint and sharply decreases in size. Mummified scabs are separated only after complete epithelialization spontaneously after 2-3 weeks. Healing proceeds without complications, especially in the absence of secondary infection, without leaving significant scars, scars or deformations of adjacent tissues or dysfunction of organs.
For topical use
Treatment of anogenital warts. Treatment is carried out on an outpatient basis under the supervision of a physician; the procedure does not require anesthesia. The drug is applied with a universal probe or applicator. After applying the drug, the color of the tissue changes to a whitish-gray color. The volume of the applied drug depends on the size of the formation and the affected area and can range from 0.02 ml to 0.2 ml. During each procedure, no more than 2-3 lesions with a total area of up to 3 cm2 can be treated. The maximum daily dose is 0.2 ml. In the presence of more extensive lesions, treatment with the drug should be carried out in several stages with an interval of at least 24 hours. When applying the drug Mardil Zinc® Max, slight swelling of the mucous membrane occurs. Within 2-3 days after using the drug, necrotic tissue is rejected. Complete regeneration is observed within 10-14 days. For large anogenital warts in case of incomplete necrosis, the drug can be re-applied after 5-7 days.
Similar drugs:
- Prostagutt mono Capsule
- Mardil Zink Maks Solution for topical use
- Prostagutt Aerosol
** The Drug Directory is intended for informational purposes only. For more complete information, please refer to the manufacturer's instructions. Do not self-medicate; Before starting to use the drug Mardil Zinc, you should consult a doctor. EUROLAB is not responsible for the consequences caused by the use of information posted on the portal. Any information on the site does not replace medical advice and cannot serve as a guarantee of the positive effect of the drug.
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Contents and release format
The product "Mardil Zinc Max" is produced in the form of a solution for topical use. The drug is a fifty percent aqueous solution of chloropropionic acid and zinc chloropropionate. 1 milliliter contains 0.5 milliliters of zinc. The product is placed in dark glass bottles. The kit comes with five glass microcapillaries with a foam container. The medicine is packaged in a cardboard box.
Indications
"Mardil Zinc Max" is prescribed for the treatment of lesions of the skin and mucous membranes in the following pathologies:
- Against the background of vulgar and anogenital warts.
- In the event of a plantar wart.
- When flat growths occur.
- With acrochordons (cutaneous horn).
- Against the background of seborrheic keratoma and seboroids.
- In case of benign nevi. For example, with low-pigment, non-pigment, papillomatous, fibroepithelial nevus, tested for benignity.
When applied topically
According to the instructions for Mardil Zinc Max, treatment for anogenital warts is carried out on an outpatient basis under the mandatory supervision of a doctor; this procedure does not require anesthesia. The drug is applied with a universal probe or using an applicator. After applying the product, the color of the fabric changes to a whitish color. The volume of medication applied directly depends on the size of the tumor and the affected area and can range from 0.02 to 0.2 milliliters. During each procedure, no more than two or three lesions with an area of up to three square centimeters are treated.
The maximum daily dosage for local use of the described medication, as in the previous case, is 0.2 milliliters. In the case of a more extensive lesion, drug therapy should be carried out in several stages with an interval of one day. When applying the drug, slight swelling of the mucous membrane may occur.
Within three days after using the medication, necrotic tissue is rejected. Complete regeneration is observed within ten to fourteen days. When large anogenital warts appear in the case of incomplete necrotization, re-application of the remedy is allowed after five to seven days. Next, let's talk about side reactions.
By-effect
In accordance with the instructions, the use of Mardil Zinc Max in rare cases can lead to changes in skin pigmentation and the formation of superficial scars. Provided that the epithelization process proceeds normally and there is a complete absence of secondary infection, and, in addition, the mummified scabs separate independently, the likelihood of such negative consequences is very small. Swelling of the tissue may be observed, although very rarely, and in case of individual sensitivity to the ingredients of the drug, various allergic reactions in the form of skin itching are possible.
About the medicine
The presented medical drug “Mardil Zinc Max” affects the body through dehydration, anticoagulation and devitalization. When used on affected areas, the drug leads to fixation and subsequent mummification of pathologically altered tissues with which the drug comes into contact. The direct effect of this drug can be expressed in discoloration of the integument and mucous membrane with the appearance of a characteristic gray tint.
Subsequently, the devitalized pathological tissues dry out and change color to a brown tint. This happens due to mummification. Mummified scabs may only come off spontaneously after complete re-epithelialization after two to three weeks. Healing occurs, as a rule, without any complications, especially in the absence of secondary infections, without leaving significant scarring and, in addition, deformation of the adjacent tissue or dysfunction of organs.
pharmachologic effect
Mardil Zinc® Max is a 50% aqueous solution of zinc chloropropionate and 2-chloropropionic acid. When applied externally and locally to affected areas of the skin or mucous membrane, the drug is able to interrupt the growth and vital activity of pathologically altered cells and tissues, incl. benign neoplasms of the skin and mucous membrane, through anticoagulation, dehydration and devitalization. When applied to affected areas, the drug leads to fixation and subsequent mummification of the pathologically altered tissue with which the drug comes into contact. The immediate effect of the drug is expressed in discoloration of the skin and mucous membrane with the appearance of a characteristic pale gray tint. Subsequently, the devitalized pathological tissue dries out and changes color to dark brown due to mummification. Mummified scabs are separated only after complete re-epithelialization spontaneously after 2-3 weeks. Healing proceeds without complications, especially in the absence of secondary infection, without leaving significant scars or scars, deformation of adjacent tissues or dysfunction of organs.
Contraindications
The use of the described medication is prohibited in a number of the following cases:
- For malignant neoplasms of the skin and mucous membrane.
- In case of a pronounced tendency to form keloids.
- During pregnancy, as well as during lactation.
- Age up to eighteen years.
- The appearance of hypersensitivity to the ingredients of the drug.
special instructions
Before opening the medicine, shake the bottle and move the solution that ends up in the upper part of the vessel to its bottom. The opened cone must be in a strictly vertical position. The described medication contains acid in its composition. Avoid contact of this medication with healthy skin or mucous membranes. If there is an accidental contact of the medicine with healthy skin or mucous membranes, then it is necessary to remove the medicine as quickly as possible using a swab moistened with water.
When treating affected areas of the skin that are located near the eyes, special precautions must be taken. Therefore, it is very important to avoid contact of this medication with your eyes. If accidental penetration of the medication into the visual organs occurs, it is necessary to urgently rinse them with a large volume of water and a one percent solution of sodium bicarbonate, and then consult a doctor. A mummified scab cannot be removed by scraping or using a mechanical instrument. The scab must separate independently from the healthy skin or mucous membrane, otherwise it is possible that the tissue healing process and scar formation may be disrupted.
Until complete healing of the skin or mucous membranes is achieved, it is not recommended to swim in the pool or in open water, and you should also try to avoid exposure to direct sunlight and ultraviolet radiation. On the day of therapy, it is recommended to limit any water procedures. It is advisable to try to avoid injury and contamination of the treated pathological lesions before the process of complete epithelialization. Before discarding the bottle, you should rinse off the remnants of this drug under running water. The empty bottle should be thrown into the trash container.
