Boric Acid

Instruction

BAR of ACID (BORIC ACID)

Storage:

Active ingredient: boric acid; 100 ml of solution contains boric acid - 3 g;

Excipients: 96% ethanol, purified water.

Medicinal form: Solution for external use, alcohol 3%.

Basic physical and chemical properties: transparent, colorless liquid.

Pharmacotherapeutic group. Antiseptic and disinfectants. Code ATX D08AD.

Pharmacological properties.

Pharmacodynamics.

The drug has an antiseptic effect. Coagulates the proteins (including enzymes) of the microbial cell, violates the permeability of the cell membrane, thereby delaying the growth and development of bacteria.

Pharmacokinetics.

When used externally, the drug is absorbed through the damaged skin, wound surface; at random use internally - through the mucous membrane of the gastrointestinal tract. Acid boron can accumulate in the tissues of the body. Exit from the body slowly.

Clinical characteristics.

Indication:

Pyoderma, peptica eczema, hypoglycaemia, acute and chronic middle otitis media.

Contraindication:

Hypersensitivity to boric acid, renal dysfunction, chronic mesotampinitis with normal or slightly altered mucous membrane, traumatic perforation of the tympanic membrane.

Special safety measures.

Do not apply the drug to large areas of the skin, do not apply for the washing of cavities. Avoid getting the drug in your eyes.

Do not violate the rules of use of the medicinal product, it can harm the health. The product can not be used after the expiration date indicated on the package.

Interaction with other drugs and other types of interactions.

Interaction is not yet known.

When using any other medicines at the same time, you should inform your doctor.

Use during pregnancy or breastfeeding.

The drug is contraindicated in women during pregnancy or breastfeeding. Ability to influence the reaction rate when driving with motor vehicles or other mechanisms. Does not affect

Method of administration and dose.

Apply externally. In pyoderma, porrland, eczema, the affected areas of the skin are treated with a napkin pre-moistened with the preparation 2-3 times a day. When otitised in the external auditory aisle, moisten the turundans with a solution or dip 3-5 drops 2-3 times a day.

Children.

Children do not use the drug.

Overdose:

In the case of accidental application of the drug internally to conduct probe gastric lavage, to appoint intra-saline laxatives, enterosorbents (activated charcoal), symptomatic therapy. Symptoms of acute poisoning: nausea, vomiting, diarrhea, impaired circulation and suppression of the central nervous system, lower body temperature, shock, coma, erythematous rash. In the case of severe poisoning, take measures to maintain vital functions of the body, conduct hemodialysis or peritoneal dialysis, replacing blood transfusion. With prolonged use of the drug on large areas of the skin, symptoms of chronic intoxication may occur: tissue swelling, depletion, stomatitis, eczema, menstrual irregularities in women, anemia, seizures, alopecia. In these cases, the drug should be discontinued, symptomatic treatment should be performed.

Side effects:

The use of the drug can cause allergic reactions (redness of the skin, itching, urticaria, rash, edema). In rare cases, the development of anaphylactic reaction, including shock; desquamation of the epithelium. Prolonged use and in patients with impaired kidney function, nausea, vomiting, diarrhea, headache, confusion, oliguria, seizures may occur. In case of occurrence of any unwanted phenomena it is necessary to consult a doctor!

Expiration date. 3 years.

Storage conditions:

Store at a temperature not exceeding 25 C.

Keep out of the reach of children.

Packaging. For 10 ml or 20 ml in vials.

Category of departure. No prescription.