30 mg/g, gel
Hydrogen peroxide
important information for the patient.
This medicine should always be used exactly as described in the patient leaflet or according to the doctor's or pharmacist's instructions.
Peroxygel 3.0 is hydrogen peroxide in the form of a gel.
The suitable form prevents the medicine from flowing out of the application site, thanks to a delicate protective film formed on the surface, which protects damaged skin.
The medicine contains hydrogen peroxide as an active substance at a concentration of 3%.
Hydrogen peroxide breaks down into water and active atomic oxygen under the influence of enzymes found in tissues and many bacteria. This reaction occurs quickly in the presence of blood, pus, and necrotic tissue. The released oxygen creates foam and removes microorganisms from the disinfected site, destroys blood cells flowing from the wound, and mechanically cleans exposed cells due to skin damage from debris of damaged tissue. Oxygen also acts as a deodorant, bleaching, and bactericidal agent. Conducted studies have confirmed that the gel acts bactericidally within 1 minute on Gram-positive bacteria (Staphylococcus aureus) and Gram-negative bacteria (Pseudomonas aeruginosa). Peroxygel 3.0 also acts fungicidally on pathogenic yeast, particularly Candida albicans, and other fungi, such as Aspergillus niger.
Peroxygel 3.0 is indicated for the disinfection of wounds, abrasions, and skin scratches.
Before starting to use this gel, the patient should discuss it with their doctor or pharmacist.
The gel should only be applied to the skin. If the gel gets on mucous membranes or in the eye area, rinse immediately with a large amount of water.
The gel should not be used in case of deep and extensive skin damage requiring immediate surgical intervention.
There is no available data on the use of Peroxygel 3.0 in children and adolescents.
The patient should inform their doctor or pharmacist about all medicines they are currently taking or have recently taken, as well as any medicines they plan to take.
No interaction studies have been conducted. The medicine should not be applied to the same skin surface as other medicines.
If the patient is pregnant or breastfeeding, thinks they may be pregnant, or plans to have a child, they should consult their doctor or pharmacist before using this medicine.
The medicine does not affect the ability to drive vehicles or operate machinery.
This medicine should always be used exactly as described in the patient leaflet or according to the doctor's or pharmacist's instructions. In case of doubts, the patient should consult their doctor or pharmacist.
Apply to the skin.
Apply 0.5-1 cm of gel directly to the wound, abrasion, or scratch. After drying, a delicate protective film forms on the damaged skin.
The medicine has thermoreversible properties. At temperatures below 20°C and above 45°C, it is a liquid. After application to the skin (temperature ~36.6°C), it takes the form of a gel.
If the patient feels that the effect of the medicine is too strong or too weak, they should consult their doctor.
Before using Peroxygel 3.0, the patient should consult their doctor or pharmacist.
No cases of overdose with Peroxygel 3.0 have been reported.
In case of using a higher dose of the medicine than recommended, the excess gel should be removed.
The patient should apply the next dose of gel. They should not use a double dose to make up for the missed dose.
In case of any further doubts about using this medicine, the patient should consult their doctor or pharmacist.
Like all medicines, Peroxygel 3.0 can cause side effects, although not everybody gets them.
A short, transient burning sensation may occur at the application site. Allergic reactions may occur.
If any side effects occur, including any possible side effects not listed in the leaflet, the patient should inform their doctor or pharmacist, or nurse.
Side effects can be reported directly to the Department of Monitoring of Adverse Reactions to Medicinal Products of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products
Al. Jerozolimskie 181C, 02-222 Warsaw
Phone: +48 22 49 21 301
Fax: +48 22 49 21 309
Website: https://smz.ezdrowie.gov.pl
Side effects can also be reported to the marketing authorization holder.
Reporting side effects will help gather more information on the safety of the medicine.
The medicine should be stored out of sight and reach of children.
The medicine should not be used after the expiry date stated on the packaging.
The expiry date refers to the last day of the specified month.
The shelf life after opening the tube is 1 year.
Store at a temperature below 25°C.
Medicines should not be disposed of via wastewater or household waste. The patient should ask their pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
Peroxygel 3.0 is a gel. The medicine packaging consists of an aluminum tube containing 10 g, 15 g, or 20 g of gel, placed in a cardboard box.
GEMIPHARMA sp. z o.o.
ul. Mickiewicza 36
05-480 Karczew
tel. +48 22 780 83 05 w. 70
e-mail: gemi@gemi.pl
Date of last update of the leaflet:03/2025
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