• On sale!
  • Save €1.51
search

BORIC ACID MV*3% UNG 30G

  • Marco Viti Farmaceutici S.p.A.
  • 030358016
Features:


Indicated for pimples and blackheads.


Indicated in case of burns and wounds.


Deductible over-the-counter drug.


Quality from Official Pharmacopoeia.


















info_outline View product sheet
Final Price €3.69
Regular Price €5.20
Save €1.51
Quantity
check_circle Available
Shipped within 24 h
  Convenient and safe payments

Even with a credit card

  Shipping in 24h all over the world

Fast and safe international shipping worldwide

  Fast returns

14 days to reconsider

  Pharmaceutical experience

Always at your service. Experts in international shipping

Other products Others products at unbeatable price

Marco Viti Farmaceutici S.p.A.

Discover all products

BORIC ACID MV*3% UNG 30G

Therapeutic indications

Antiseptic for the disinfection of minor burns and irritated or chapped skin areas. The ointment also has a decongestant action. Boric acid is indicated as an antibacterial for the treatment of acne.

Dosage and method of use

External use: apply as needed to the affected area.Adults: Boric acid can be applied directly once or twice daily to inflamed areas for chapped, irritated or dry skin, abrasions, mild sunburn, sunburn, windburn or insect bites.Children over 3 years old: Boric acid can be applied directly once or twice daily to inflamed areas associated with chapped, irritated, or dry skin, diaper rash, mild sunburn, sunburn, windburn, or insect bites.

Contraindications

Boric acid is contraindicated in case of: - hypersensitivity to the active ingredient or to any of the excipients listed in paragraph 6.1; - extensive skin lesions; - children under 3 years of age.

Side effects

The absorption of boric acid through intact skin is less than 0.5%; however, it may increase if accidentally administered systemically or applied to wounds or lesions. Below are the side effects of boric acid that occurred in case of accumulation toxicity, after prolonged exposure and following systemic absorption. These effects are organized according to the MedDRA system organic classification. There is insufficient data to establish the frequency of the individual effects listed.Pathologies of the skin and subcutaneous tissue: Dermatitis, skin rashes, alopecia.Gastrointestinal disorders. Gastro-intestinal disorders: nausea, vomiting, diarrhea.Metabolism and nutrition disorders: Anorexia.Endocrine disorders: Menstrual disorders.Pathologies of the blood and lymphatic system: Anemia.Pathologies of the musculoskeletal system and connective tissue: Weakness.Psychiatric disorders: Confusion.Nervous system disorders: Convulsions.Reporting of suspected adverse reactions.Reporting 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: www.agenziafarmaco.gov.it/it/responsabili.

Special warnings

Excessive and prolonged application on large areas or damaged skin may cause accumulation toxicity. Keep out of reach of children, as deaths have occurred following accidental ingestion. The medicine must not be used for ophthalmic use.

Pregnancy and breastfeeding

Pregnancy: No clinical data on exposed pregnancies are available. Animal studies are insufficient to demonstrate effects on embryonic/foetal development (see section 5.3). The potential risk for humans is not known, however if the medicine is used in accordance with the instructions for use, absorption is poor and the risk of systemic effects is minimal.Feeding time: There are no data available on the use of the medicine during breastfeeding and it is not known whether this active ingredient passes into breast milk. However, since the absorption of the drug can be considered negligible, it is very unlikely that significant quantities reach the breast milk.

Expiration and conservation

Keep the container tightly closed in order to protect the medicine from light.

Interactions with other drugs

There are no known interactions between boric acid for external use and other medicines.

Overdose

The risk of acute intoxication via the skin appears to be a negligible event given its low transcutaneous absorption rate. Boric acid can be absorbed in toxic quantities through the gastrointestinal tract, by inhalation or through skin lesions.SymptomsCases of poisoning and death have occurred following the use of large quantities of boric acid on wounds or sores, especially in children. The mechanism of toxic action is unknown and numerous organs and systems are affected, in particular the skin, kidney and digestive tract. The toxic effects also affect the CNS and the lung with lesions, mainly haemorrhagic, of obscure origin. The main symptoms of boric acid poisoning are vomiting, diarrhea, visceral pain, flaking skin erythema, CNS stimulation followed by depression, restlessness, headache. Metabolic acidosis and serious salt and water imbalances are also frequent. Furthermore, boric acid in these situations can cause convulsions, changes in body temperature and kidney damage which can be evidenced by oliguria. Death, following circulatory collapse and untreated shock, can occur within 3 to 5 days. Cyanosis, delirium, seizures, and coma (HSDB) may also occur. Cases of serious intoxication manifested themselves with gastrointestinal disorders (73%), central nervous system disorders (67%) and skin lesions (76%). Symptoms of chronic poisoning include anorexia, confusion, debilitation, dermatitis, menstrual disorders, anemia, convulsions and alopecia (see section 4.8).TreatmentNo treatment is necessary if the dose taken is less than 50 mg/kg. For ingestion of higher doses, gastric lavage is carried out with suspension of activated charcoal and saline purgative. If the absorbed quantity exceeds 100 mg/kg, even if the patient is still asymptomatic, forced diuresis must be instituted immediately, in order to accelerate elimination and protect the kidney from toxic effects; at the first signs of renal failure and water overdose, forced diuresis should be replaced with peritoneal dialysis or hemodialysis. The remaining therapy is symptomatic and resuscitative.

Active principles

100 g of ointment contains: active ingredient: boric acid 3 g. For the full list of excipients, see section 6.1.

Excipients

White Vaseline.

030358016

Data sheet

Packaging
3% ointment 30 g
Product Type
HUMAN DRUG
ATC code
D08AD
ATC description
Boric acid and derivatives
Therapeutic Group
Antiseptics
Active principle
boric acid (FU)
Class
C.
Pharmaceutical form
ointment
Type of Administration
topical
Container
tube
Quantity
1 tube
Capacity
30 grams
Quantity of the Active Ingredient
3G
Recipe required
SOP - non-prescription medicine
chat Comments (0)