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Viatris Healthcare

Betadine 10% cutaneous solution 120ml

Betadine 10% cutaneous solution 120ml

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Betadine 10% skin solution 120ml is a povidone-iodine -based disinfectant , indicated for cleaning and antisepsis of damaged skin in the case of superficial wounds and small bedsores . It forms a brown protective film that does not stain, with a high antimicrobial action , ideal for preventing skin infections and promoting daily hygiene of damaged skin.

NET WEIGHT OF THE PRODUCT

120ml

EAN

023907292

MINSAN

023907292

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Betadine 10% skin solution 120ml is a disinfectant product formulated for cleaning and disinfection of damaged skin, ideal for treating small superficial wounds and bedsores with limited involvement of the epidermis. The active ingredient, Povidone iodine, is present at 10% iodine, ensuring effective antimicrobial action. This solution is particularly suitable forskin antisepsis, forming a brown protective film that does not stain. The formulation includes excipients such as Glycerol, Macrogol laurel ether, and Dibasic sodium phosphate dihydrate, which contribute to the stability and effectiveness of the product. Betadine 10% skin solution is an essential ally for the management of small skin lesions, offering reliable protection against infections.

INDICATIONS

Why is Betadine 10% cutaneous solution 120ml used? What is it for?

Disinfection and cleaning of damaged skin (small superficial wounds, bedsores with limited involvement of the epidermis).

ACTIVE INGREDIENTS AND EXCIPIENTS

What is the composition of Betadine 10% skin solution 120ml?

Composition

Betadine 10% cutaneous solution 100 ml contain: Active ingredient: Povidone iodine (10% iodine) 10 g For the complete list of excipients.

Excipients

Betadine 10% cutaneous solution: Glycerol, Macrogol lauryl ether, Dibasic sodium phosphate dihydrate, Citric acid monohydrate, Sodium hydroxide, Purified water.

DOSAGE

How is Betadine 10% cutaneous solution 120ml taken?

Betadine 10% skin solution: It is applied 2 times a day directly on small wounds and skin infections. A quantity of 5 ml of solution (containing 50 mg of iodine) is sufficient to treat an area of ​​approximately 15 cm on each side. For skin antisepsis: apply a protective layer of the brown solution until a medium intensity color is obtained: a non-staining surface film is formed.

CONTRAINDICATIONS AND SIDE EFFECTS

When should Betadine 10% cutaneous solution 120ml not be used and what side effects can it cause?

Contraindications

Hypersensitivity to the active substance or to any of the excipients (see the section "What is the composition of Betadine 10% skin solution 120ml?"). Hyperthyroidism Do not use in children under six months of age.

Side effects

Undesirable effects are classified according to their frequency: Very common (≥ 1/10) Common (> 1/100 to less than 1/10) Uncommon (≥ 1/1,000 to less than 1/100) Rare (≥ 1/10,000 to less than 1/1,000) Very rare (less than 1/10,000) Not known (the frequency cannot be defined on the basis of available data) Immune system disorders Rare: Hypersensitivity Very rare: Anaphylactic reaction Endocrine disorders Very rare: Hyperthyroidism* (sometimes with symptoms such as tachycardia or agitation) Not known: Hypothyroidism *** Metabolism and nutrition disorders Not known: Electrolyte imbalance **, Metabolic acidosis ** Skin and subcutaneous tissue disorders Rare: Contact dermatitis (with symptoms such as erythema, microvesicles and pruritus) Very rare: Angioedema Not known: Exfoliative dermatitis Renal and urinary disorders Not known: Acute renal failure **, Abnormal blood osmolarity ** *In patients with a history of thyroid disease (see section Warnings and special precautions for use) following high iodine uptake, for example after long-term use of povidone iodine solution to treat wounds and burns on areas extensive skin. **May occur following the uptake of high quantities of povidone iodine (for example in the treatment of burns) ***Hypothyroidism following prolonged or extensive use of povidone iodine Reporting of suspected adverse reactions Reporting of suspected adverse reactions that occur after authorization of the medicinal product is important, as it allows continuous monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the national reporting system at: http://www.agenziafarmaco.gov.it/content/come-segnalare-una-sosp etta-reazione-avversa.

INTERACTIONS

Which medicines or foods can modify the effect of Betadine 10% skin solution 120ml?

Avoid the simultaneous use of other antiseptics and detergents. The polyvinylpyrrolidone-iodine complex is effective at pH values ​​between 2.0 and 7.0. It is possible that the complex reacts with proteins or other unsaturated organic compounds, and this leads to a reduction in its effectiveness. The concomitant use of preparations with enzymatic components for the treatment of wounds leads to a weakening of the effects of both substances. Povidone iodine should not be used simultaneously with products containing mercury salts or benzoin compounds, carbonates, tannic acid, alkali, hydrogen peroxide, taurolidine and silver. The use of povidone iodine-containing products concomitantly with other octedin-containing antiseptics in the same or adjacent sites may cause temporary dark discoloration of the affected areas. The oxidative effect of povidone iodine preparations can cause false positive results of some laboratory diagnostic tests (for example tests with toluidine or guaiac gum for the determination of hemoglobin or glucose in feces or urine). Avoid habitual use in patients receiving concomitant treatment with lithium. Absorption of iodine from povidone iodine solution may reduce thyroid iodine uptake. This may interfere with various tests (thyroid scan, determination of iodine-binding proteins, radioactive iodine diagnostics) and may make planned treatment of the thyroid with iodine (radioactive iodine therapy) impossible. After the end of treatment, an adequate period of time must pass before performing a new scan.

PREGNANCY AND BREASTFEEDING

Can Betadine 10% cutaneous solution 120ml be used during pregnancy and breastfeeding?

During pregnancy and breastfeeding, povidone iodine solution should be used only if strictly necessary and at the lowest possible dose, due to the ability of iodine to cross the placenta and be secreted into breast milk and the high sensitivity of the fetus and newborn to iodine. Furthermore, iodine is more concentrated in breast milk than in serum, therefore it can cause transient hypothyroidism with an increase in TSH (thyroid stimulating hormone) in the fetus or newborn

WARNINGS

What are the warnings of Betadine 10% skin solution 120ml?

Warnings and precautions

For external use only. This medicine must not be applied to severely damaged skin and large surfaces. Do not use for prolonged treatments: use, especially if prolonged, may give rise to sensitization phenomena. In this case, treatment should be discontinued and a clinical evaluation performed. Particular caution should be used in patients with pre-existing renal insufficiency who require regular applications of Betadine on damaged skin. Patients with goiter, thyroid nodules, or other acute and non-acute thyroid conditions are at risk of developing thyroid hyperfunction (hyperthyroidism) following administration of large amounts of iodine. In this patient population, povidone iodine solution should not be used for a prolonged period of time and on large body surfaces. Even after the end of treatment, it is necessary to look for early symptoms of possible hyperthyroidism and monitor thyroid function. Do not use at least 10 days before performing a scan or after a radioactive iodine scan or in the treatment of thyroid cancer with radioactive iodine. The pediatric population is at greater risk of developing hypothyroidism following applications of high doses of iodine. Due to the permeability of the skin and their high sensitivity to iodine, the use of povidone iodine should be reduced to the bare minimum in children. A check of the child's thyroid function (for example T4 and TSH levels) may be necessary. Any oral ingestion of povidone iodine by the child should be avoided. In pediatric age use only under strict supervision and in cases of actual need. Accidental ingestion or inhalation of some disinfectants can have serious, sometimes fatal consequences. Avoid contact with eyes.

Overdose

In case of overdose, whether intentional or accidental, hypothyroidism or hyperthyroidism may occur. Systemic absorption of iodine after repeated applications of the product on large wounds or severe burns may produce a number of symptoms such as: metallic taste, increased salivation, burning or stinging in the mouth and throat, irritation or swelling of the eyes, fever, skin rash, diarrhea and gastrointestinal disorders, hypotension, tachycardia, metabolic acidosis, hypernatremia, failure of renal function, pulmonary edema and shock. In case of accidental ingestion of large quantities of product, institute symptomatic and supportive treatment with particular attention to electrolyte balance and renal and thyroid function.

Driving vehicles and using machinery

Betadine does not affect the ability to drive or use machines.

CONSERVATION

How is Betadine 10% cutaneous solution 120ml stored?

Betadine 10% cutaneous solution: store at temperatures not exceeding 25°C

FORMAT

What is the format of Betadine 10% cutaneous solution 120ml?

120ml

DRUG LEGAL TEXT

Content responsibility

This sheet contains information that is not intended to replace a doctor's diagnosis or advice, as only the doctor can draw up any prescription and give therapeutic indications. All contents must be understood and are of an exclusively informative nature and aimed exclusively at bringing to the attention of customers or potential customers in the pre-purchase phase of the products sold through this site. In case of pathologies, disorders or allergies it is always best to consult your doctor first.

Please note

The product names, ingredients and percentages indicated in the descriptions are purely indicative and may be subject to changes or updates by the manufacturing companies. Due to the impossibility of adapting to these updates in real time, the photos and technical information of the products included on Dottortili.com may differ from those shown on the label or otherwise disseminated by the manufacturing companies. The only identification element appears to be the ministerial code MINSAN. The online pharmacy Dottortili.com does not guarantee the truthfulness and timeliness of the information published and declines any responsibility for any errors, omissions or failure to update the same. Dottortili.com assumes no responsibility for damages of any nature that may arise from access to the information published.

Data source: Farmadati Italia

Website: www.farmadati.it

The Farmadati Italia database is used by almost all pharmacies, parapharmacies, herbalist shops, health shops, large-scale retail trade, computerized doctors, etc. thanks to the guarantee of historical reliability, seriousness and professionalism of the company on the national territory.

The Farmadati Italia S.r.l management system complies with the requirements of the UNI EN ISO 9001:2015 standards for quality management systems and UNI CEI ISO/IEC 27001:2017 for information security management systems.

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Responsibility for content
This sheet contains information that is not intended to replace a diagnosis or medical advice, as only a doctor can write any prescription and give therapeutic indications. All contents must be understood and are of an exclusively informative nature and aimed exclusively at bringing to the attention of customers or potential customers in the pre-purchase phase of the products sold through this site. In case of pathologies, disorders or allergies it is always best to consult your doctor first.

Please note
The names of the products, the ingredients and the percentages indicated in the descriptions are purely indicative, they could be subject to changes or updates by the manufacturing companies. Due to the impossibility of adapting in real time to such updates, the photos and technical information of the products inserted on Dottortili.com may differ from those reported on the label or otherwise disseminated by the manufacturing companies. The only identification element is the ministerial code MINSAN. The online pharmacy Dottortili.com does not guarantee the truthfulness and timeliness of the information published and declines all responsibility for any errors, omissions or failure to update the same. Dottortili.com does not assume responsibility for damages of any nature that may arise from access to the published information.

Data source: Farmadati Italia
Website: www.farmadati.it

The Farmadati Italia Database is used by almost all pharmacies, parapharmacies, herbalists, health shops, large-scale retail trade, computerized doctors, etc. thanks to the company's historical guarantee of reliability, seriousness and professionalism on the national territory.

The Farmadati Italia Srl management system complies with the requirements of the UNI EN ISO 9001:2015 standards for quality management systems and UNI CEI ISO/IEC 27001:2017 for information security management systems.