Hexetidine (Bactidol) 0.1% solution is a brilliantly clear reddish-pink liquid with a modified mint flavor, free from sediment and suspended particles.
Each 100 mL contains: Hexetidine 100 mg, alcohol 9%.
Hexetidine (Bactidol) 0.1% Solution is indicated for its antibacterial and antifungal action in the following circumstances: Minor oropharyngeal infections and inflammatory conditions including candidiasis.
As an aid in the prevention and treatment of gingivitis.
In the management of sore throat and recurrent aphthous ulcers.
Alleviation of halitosis.
Pre- and post-oropharyngeal surgery.
Daily oral hygiene including the prevention and control of dental plaque.
Adults and children 12 years and over: Rinse the mouth or gargle for 30 seconds with 10 to 20 mL of undiluted Hexetidine (Bactidol) 0.1% Solution or apply the product using a cotton wool swab for 2 to 3 minutes, not to exceed 3 times daily.
Do not swallow the solution but spit out after use.
Not recommended for children under 12 years of age.
Hexetidine, at the strength present in hexetidine products, is unlikely to be toxic when used as directed.
There is no evidence to suggest that repeated, excessive administration of hexetidine would lead to hypersensitivity-type reactions.
Ingestion of sufficient quantities of hexetidine in alcoholic solution may lead to signs/symptoms of alcohol intoxication.
In the event of overdose, get medical help or contact a Poison Control Center right away.
What to do when the patient has taken more than the recommended dosage: Consult the doctor if the patient has taken more than the recommended dosage.
Hypersensitivity to hexetidine or to any of the ingredients.
For local use only. Do not swallow.
If symptoms persist or worsen, or if new symptoms occur, stop use and consult a physician.
Long term use is not recommended (not to exceed 10 days usage without consulting a doctor or dentist for further use).
When should the patient consult their doctor: If symptoms persist or worsen, or if new symptoms occur, stop use and consult the doctor.
Effects on Ability to Drive or Use Machines: Hexetidine has no known effect on the ability to drive and use machines.
There are no adequate and well-controlled studies in pregnant or breastfeeding women for hexetidine. It is not known whether hexetidine or its metabolites are excreted in breast milk. Negligible amount of hexetidine is systemically absorbed; it is unlikely that use of hexetidine during pregnancy or lactation will present a risk to the fetus or nursing infant.
However as with other products, hexetidine should not be used during pregnancy or lactation unless the potential benefit of treatment to the mother outweighs the possible risks to the developing fetus or nursing infant. Ask a physician before use if you are pregnant or breastfeeding.
Post Marketing Data: Adverse drug reactions (ADRs) identified during Post-marketing experience with hexetidine are included. The frequencies are provided according to the following convention: Very common ≥1/10; Common ≥1/100 and <1/10; Uncommon ≥1/1,000 and <1/100; Rare ≥1/10,000 and <1/1,000; Very rare <1/10,000; Not known (cannot be estimated from the available data).
In the table as follows, ADRs identified are presented by frequency category based on incidence in adequately designed clinical trials or epidemiology studies, if available or when incidence is unavailable, frequency category is listed as Not known. (See table.)
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There are no known drug interactions for hexetidine.
Store at temperatures not exceeding 30°C.
A01AB12 - hexetidine ; Belongs to the class of local antiinfective and antiseptic preparations. Used in the treatment of diseases of the mouth.
Bactidol oral soln 0.1%
120 mL x 1's;250 mL x 1's;30 mL x 1's;500 mL x 1's;60 mL x 1's
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