Leaflet: information for the user
Clorxil 20 mg/ml solution for cutaneous spraying
chlorhexidine digluconate
Read the entire leaflet carefully before starting to use this medicine, as it contains important information for you.
Contents of the leaflet
5 Conservation of Clorxil
Clorxil contains chlorhexidine digluconate, used as a skin antiseptic.
It is indicated as a skin antiseptic before performing invasive medical procedures, such as punctures, injections, catheter insertion, and preoperative field in surgeries, catheter maintenance, and surgical suturing in adults and children.
Do not use Clorxil
Warnings and precautions
Consult your doctor or pharmacist before starting to use Clorxil
This medicine is for external use only. Do not ingest or inhale.
Do not use excessive amounts and avoid accumulating the solution in skin folds, under the patient, or soaking bedding or other materials in direct contact with the patient. Do not let the solution stagnate.
This medicine may, in rare cases, cause severe allergic reactions leading to a decrease in blood pressure and even loss of consciousness. The first symptoms of a severe allergic reaction may be skin rash or asthma. If you notice these symptoms, stop using this medicine and contact your doctor as soon as possible (see section 4: "Possible side effects").
Avoid prolonged contact with the skin.
This medicine should not be applied:
Severe cases of persistent corneal injury (injury to the surface of the eye) that could require a corneal transplant have been reported when similar products have accidentally come into contact with the eyes during surgical interventions in patients under general anesthesia (deep sleep induced without pain).
This medicine should only be applied gently to the skin. If the solution is applied too vigorously to fragile or sensitive skin, or after repeated use, a local skin reaction may occur with erythema, inflammation, itching, dry skin, and/or peeling and localized pain in the administration area. At the first sign of any of these reactions, administration of this medicine should be stopped.
Children
Use with caution in neonates, especially in premature babies. Clorxil can cause chemical burns to the skin.
This medicine should only be used under medical prescription in children under 30 months.
Other medicines and Clorxil
Inform your doctor or pharmacist if you are using, have recently used, or may need to use any other medicine.
Inform your doctor or nurse if you have recently been administered a vaccine or an injection for a skin test (epicutaneous tests to detect allergies).
The simultaneous or successive use of other antiseptics should be avoided to minimize the risk of possible interference between them.
The product is incompatible with anionic derivatives (soaps), so the skin should be rinsed well after cleaning.
Pregnancy, breastfeeding, and fertility
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor before using this medicine.
It is unknown whether chlorhexidine digluconate is excreted in breast milk. Since many medicines are excreted in breast milk, caution should be exercised when administering Clorxil to breastfeeding women.
Driving and using machines
Clorxil does not affect the ability to drive or operate machines.
Apply the product gently to the area of skin that needs to be prepared. Spray as many times as necessary depending on the medical procedure. Each spray is equivalent to a volume of 130 microliters. Do not dilute.
The product should be applied directly to the area to be treated and allowed to dry before any procedure.
In case of doubt, ask your doctor or nurse.
If you use more Clorxil than you should
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service, phone: 91 562 0420, indicating the medicine and the amount ingested.
Like all medicines, this medicine can cause side effects, although not everyone gets them.
The very rare side effects (less than 1 in 10,000 people) observed in the skin and subcutaneous tissue are:
Skin irritation, including: erythema, rash, urticaria, pruritus, and blisters or vesicles in the administration area. Other local symptoms may be: burning sensation on the skin, pain, and inflammation.
Other side effects with an unknown frequency (cannot be estimated from the available data) are:
-Allergic reactions including anaphylactic shock.
-Corneal injury (injury to the surface of the eye) and permanent eye injury, including permanent vision loss (after accidental eye exposure during surgical interventions in the head, face, and neck) in patients under general anesthesia (deep sleep induced without pain).
-Pain, hyperemia, and chemical burns in cases of accidental contact.
-Dermatitis, eczema, urticaria, skin irritation, blisters.
-Chemical burns in neonates.
Stop using Clorxil and seek medical attention immediately if you experience any of the following reactions: swelling of the face, lips, tongue, or throat; red and itchy skin rash; wheezing or difficulty breathing; feeling of fainting and dizziness; strange metallic taste in the mouth; collapse. You may be having an allergic reaction.
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 leaflet. You can also report them directly through the Spanish Medicines and Health Products Agency (AEMPS) http://www.notificaram.es. By reporting side effects, you can contribute to providing more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiration date shown on the label after Cad. The expiration date is the last day of the month indicated.
No special storage conditions are required
Medicines should not be thrown down the drain or into the trash. Ask your pharmacist how to dispose of the packaging and medicines you no longer need. This will help protect the environment.
Composition of Clorxil
Per ml of solution:
The active ingredient is: chlorhexidine digluconate 20 mg.
The excipient is purified water.
Each ml of solution contains: 20 mg of chlorhexidine digluconate.
Appearance of the product and contents of the package
Transparent and colorless solution presented in white HDPE plastic bottles
with a white PP/PE spray valve. It is presented in:
Marketing authorization holder and manufacturer
LABORATORIOS BOHM, S.A.
C/ Molinaseca 23-25. Polígono Industrial Cobo Calleja.
28947 Fuenlabrada (Madrid)
Phone: 91 642 18 18
Fax: 91 642 0572
Email: info@bohm.es
Date of the last revision of thisleaflet:
April 2023
Detailed information about this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/)