Package Leaflet: Information for the User
Topigel 200mg/goral gel
Read the entire package leaflet carefully before starting to use this medication, as it contains important information for you.
Follow the administration instructions for the medication contained in this package leaflet or as indicated by your doctor or pharmacist.
Contents of the Package Leaflet
It is a topical anesthetic that acts by suppressing pain when applied externally to the area of the
mouth to be treated.
It is indicated for the local relief of dental or mouth pain, such as that caused by friction from prostheses,
extractions, small mouth sores, canker sores, and small ulcers in adults and children from 6 years old.
You should consult a doctor if it worsens or does not improve after 2 days of treatment.
Do not use Topigel
Warnings and Precautions
Consult your doctor, pharmacist, or nurse before starting to use Topigel
dizziness, shallow breathing, nausea, fatigue, or tachycardia.
Interaction with Other Medications
Tell your doctor or pharmacist if you are using, have recently used, or may need to take any other medication.
This medication may interact with:
Use of Topigel with Food and Drinks
Do not use this medication before meals or before drinking (see warnings and precautions section).
Pregnancy and Breastfeeding
If you are pregnant or breastfeeding, or think you may be pregnant or plan to become pregnant, consult your doctor or pharmacist before using this medication.
Do not use benzocaine during pregnancy.
It is not known if benzocaine is excreted in breast milk, so breastfeeding women should not use this medication.
Use in People Over 65 Years Old
People over 65 years old and debilitated patients may be more sensitive to the adverse effects of benzocaine, so they should consult their doctor.
Driving and Using Machines
It does not affect driving or using machines.
Follow the administration instructions for the medication contained in this package leaflet or as indicated by your doctor or pharmacist. In case of doubt, ask your doctor or pharmacist.
This medication is for administration in the mouth. Do not swallow.
The recommended dose is:
Adults and adolescents:
Apply a small amount of the medication to the area to be treated, with small touches, up to 3 or 4 times a day.
Children 6-12 years old: only under adult supervision, as in the previous case.
Children 2-6 years old: under medical control
Children under 2 years old: under strict medical control.
Do not apply this medication more than 3 or 4 times a day.
If it worsens or if the pain persists after 2 days of treatment, consult a doctor.
Wash your hands after applying the medication.
If You Use More Topigel Than You Should
Signs of overdose may be: bluish discoloration of the skin, slurred speech, numbness, staggering gait, blurred or double vision, dizziness, excitement, or convulsions, ringing in the ears, increased sweating. It can also decrease blood pressure.
In case of overdose or accidental ingestion, consult a doctor immediately or go to a medical center or call the Toxicology Information Service (phone 91 562 04 20), indicating the medication and the amount ingested.
Like all medications, Topigel can cause side effects, although not all people experience them.
During the use of benzocaine, the following side effects have occurred, whose frequency cannot be established with certainty:
Hives, edema, anaphylactoid reaction (contact dermatitis). Cross-reactions with other local anesthetics of the ester type. Photosensitivity, bad taste in the mouth, dehydration of the mucous membranes, and difficulty swallowing.
Burning sensation in the mouth Methemoglobinemia, whose symptoms are: headache, dizziness, shallow breathing, nausea, fatigue, or tachycardia.
Prolonged contact of benzocaine with mucous membranes can cause dehydration of the epithelium and hardening of the mucous membranes.
Reporting Side Effects
If you experience any type of side effect, consult your doctor or pharmacist, even if it is a possible side effect not listed in this package leaflet. You can also report them directly through the Spanish Medication Surveillance System website:
www.notificaram.es.
By reporting side effects, you can contribute to providing more information on the safety of this medication.
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date shown on the packaging after CAD. The expiration date is the last day of the month indicated.
Do not store at a temperature above 30°C. Keep the packaging perfectly closed to protect it from light.
Medications should not be thrown away through the sewers or in the trash. Deposit the packaging and medications you no longer need at the SIGRE point in the pharmacy. In case of doubt, ask your pharmacist how to dispose of the packaging and medications you no longer need. This way, you will help protect the environment.
Composition of Topigel
? The active ingredient is: Benzocaine.
? The other components are: Polyethylene glycol, Saccharin, Cherry flavor.
Appearance of the Product and Package Contents
Topigel is a viscous gel with a cinnamon color and cherry flavor.
It comes in a polyethylene tube of 11.25g and 33.75g of gel.
Marketing Authorization Holder
Laboratorios Clarben S.A.
Av Valdelaparra 27
28108 Alcobendas, Spain.
Manufacturer
INDUSTRIA QUIMICA Y FARMACEUTICA VIR, S.A.
Laguna, 66-68-70. Poligono Industrial Urtinsa II
28923 Alcorcón (Madrid), Spain
This Package Leaflet was Approved in
December 2013
Detailed and updated information on this medication is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/