Patient Information Leaflet
Normosept 10 mg/ml Cutaneous Solution for Pulverization
Chlorhexidine Digluconate
Read this leaflet carefully before you start using this medicinebecause it contains important information for you
Follow exactly the administration instructions for the medicine contained in this leaflet or those indicated by your doctor, pharmacist or nurse.
1.What is Normosept and what it is used for
2.What you need to knowbeforestarting touse Normosept
3.How to use Normosept
4.Possible side effects
5.Storage of Normosept
6.Contents of the package and additional information
It is a topical medication that contains chlorhexidine as the active ingredient. Chlorhexidine is an antiseptic that is applied to the skin.
It is indicatedas a wound antiseptic and for minor skin burns and as umbilical cord antiseptic in newborns (see section 2 “Warnings and precautions”).
If symptoms worsen after 5 days, consult your doctor.
No use Normosept:
-If you are allergic (hypersensitive) to chlorhexidine or any of the other components of this medication (listed in section 6).
Do not use in eyes or ears, or in the interior of the mouth or other mucous membranes.
Warnings and precautions
Consult your doctor or pharmacist before starting to use Normosept.
-In case of accidental contact with ears, wash immediately with plenty of water.
-Normosept should not come into contact with the eyes due to the risk of visual injury. If it comes into contact with the eyes, wash immediately and abundantly with water. In cases of eye irritation, redness, or pain, or visual disturbances, consult a doctor immediately.
Severe cases of persistent corneal injury (injury to the surface of the eye) have been reported, which could require a corneal transplant when similar products have accidentally entered the eyes during surgical procedures, in patients under general anesthesia (deep, painless sleep).
-Do not use in case of deep and extensive wounds without consulting a doctor.
-Do not apply repeatedly, or use on large areas, with occlusive dressing (non-breathable), on injured skin and in mucous membranes.
-Clothing that has come into contact with this medication should not be washed with bleach or other hypochlorites, as this would cause a brownish discoloration of the tissues, but with domestic detergents based on sodium perborate.
-Do not use for the asepsis of puncture or injection sites, or for the disinfection of surgical material.
-Use with caution in newborns, especially premature infants. Normosept can cause chemical burns on the skin.
-Consult your doctor before using in children under 30 months.
Use of Normosept with other medications
-Inform your doctor or pharmacist if you are using, have used recently, or may need to use any other medication.
-It is recommended to avoid the use of multiple antiseptics at the same time or in succession, except with other cationic compounds.
-Do not use in combination or after the application of anionic soaps (soaps), acids, heavy metal salts, and iodine, so the skin should be thoroughly rinsed after cleaning.
Pregnancy and lactation
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.
Driving and operating machines
The influence of Normosept on the ability to drive and operate machines is negligible or insignificant.
Follow exactly the medication administration instructions contained in this leaflet or those indicated by your doctor or pharmacist. If in doubt, ask your doctor or pharmacist.
Use without dilution.
It is recommended to clean and dry the wound before applying Normosept. Apply to the affected area, or on a gauze, one or two times a day. Do not perform more than two daily applications of the product.
If you use more Normosept than you should
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicological Information Service, phone: 91 562 04 20, indicating the medication and the amount ingested.
Like all medications, Normosept may produce adverse effects, although not everyone will experience them.
Reactions to the skin may occur.
Other possible adverse effects, for which the frequency is unknown, are:
If you consider that any of the adverse effects you are experiencing are severe or if you notice any adverse effects not mentioned in this prospectus, inform your doctor or pharmacist.
Reporting Adverse Effects
If you experience any type of adverse effect, consult your doctor, pharmacist, or nurse, even if it is possible adverse effects that do not appear in this prospectus. You can also report them directly through the Spanish System for Pharmacovigilance of Medicinal Products for Human Use:www.notificaRAM.es. By reporting adverse effects, you can contribute to providing more information about the safety of this medication.
Keepthis medicationout of the sight and reach of children.
No special storage conditions are required.
Do not usethis medicationafter the expiration date that appears onthe boxafter CAD. The expiration date is the last day of the month indicated.
Medicines should not be disposed of through drains or in the trash.Deposit the packaging and unused medications at the SIGRE collection pointat the pharmacy.If in doubt, ask your pharmacisthow to dispose ofthepackaging and unusedmedications.By doing so, you will help protect the environment.
Composition of Normosept
Appearance of the product and contents of the packaging
Normosept is a transparent and colorless solution.
It is presented in a polyethylene terephthalate (PET) bottle, provided with a spray valve, containing 25 ml.
Holder of the marketing authorization and responsible for manufacturing
LABORATORIOS NORMON, S.A.
Ronda de Valdecarrizo, 6 – 28760 Tres Cantos – Madrid (Spain)
Date of the last review of this leaflet:June 2024
The detailed and updated information on this medication is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS) http://www.aemps.gob.es/
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