Rivanol 0,1%
Ask a doctor about a prescription for Rivanol 0,1%
How to use Rivanol 0,1%
Leaflet attached to the packaging: information for the user
RIVANOL 0.1%, 1 mg/g, liquid for the skin
(Ethacridini lactas monohydricus)
Please read carefully the contents of the leaflet before using the medicine, as it contains 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.
- Please keep this leaflet, so you can read it again if you need to.
- If you need advice or additional information, you should consult a pharmacist.
- If the patient experiences any side effects, including any possible side effects not listed in the leaflet, they should inform their doctor or pharmacist. See section 4.
- If there is no improvement or the patient feels worse, they should contact their doctor.
Table of contents of the leaflet
- 1. What is Rivanol 0.1% and what is it used for
- 2. Important information before using Rivanol 0.1%
- 3. How to use Rivanol 0.1%
- 4. Possible side effects
- 5. How to store Rivanol 0.1%
- 6. Contents of the packaging and other information
1. What is Rivanol 0.1% and what is it used for
Rivanol 0.1% is a liquid for application to the skin. Rivanol 0.1% contains the active substance ethacridine lactate monohydrate, which belongs to the group of acridine dyes with antibacterial action. Ethacridine lactate monohydrate acts on streptococci, staphylococci, and other Gram-positive bacteria.
Indications
Disinfection of the skin and superficial skin damage (e.g., abrasions).
2. Important information before using Rivanol 0.1%
When not to use Rivanol 0.1%:
- if the patient is allergic to the active substance or acridine dyes,
- orally,
- in the eyes.
Warnings and precautions
Before starting to use Rivanol 0.1%, the patient should discuss it with their doctor or pharmacist.
Do not use the medicine for a long time, as it may cause allergic reactions.
Do not use on large areas of damaged skin.
Avoid contact between the medicine and clothing.
Use should be stopped if symptoms of an allergy occur.
Rivanol 0.1% and other medicines
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.
Due to the risk of inactivation of the medicine, it should not be used at the same time as oxidizing agents (potassium permanganate, hydrogen peroxide), tannins (tannin), anionic substances (polyethylene glycol), or a solution of sodium borate, salicylic acid, sodium chloride.
Pregnancy, breastfeeding, and fertility
If the patient is pregnant or breastfeeding, thinks they may be pregnant, or plans to have a child, they should consult their doctor before using this medicine.
There is no data on the use of the medicine during pregnancy and breastfeeding.
Driving and using machines
When used correctly, the medicine has not been shown to affect the ability to drive vehicles or operate machinery.
3. How to use Rivanol 0.1%
This medicine should always be used exactly as described in the patient leaflet or according to the doctor's or pharmacist's instructions. If in doubt, the patient should consult their doctor or pharmacist.
The medicine is intended for local use on the skin.
Unless the doctor recommends otherwise, the medicine is usually applied several times a day in the form of dressings, compresses, and rinses.
Use in children
There is no data on the use of the medicine in children.
If the patient feels that the effect of Rivanol 0.1% is too strong or too weak, they should consult their doctor.
Using a higher dose of Rivanol 0.1% than recommended
There is no data available on overdosing with the medicine when used according to the indications and recommended method of use.
Missing a dose of Rivanol 0.1%
If a dose of Rivanol 0.1% is missed, the patient should continue treatment using the medicine as usual, according to the instructions.
If the medicine is accidentally ingested, the patient should immediately contact their doctor.
4. Possible side effects
Like all medicines, Rivanol 0.1% can cause side effects, although not everybody gets them.
Prolonged use of the medicine may cause allergic reactions.
If any of the side effects get worse or if the patient experiences any side effects not listed in the leaflet, they should inform their doctor or pharmacist.
Reporting side effects
If the patient experiences any side effects, including any possible side effects not listed in the leaflet, they 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 181 C, 02-222 Warsaw, tel.: +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 to gather more information on the safety of the medicine.
5. How to store Rivanol 0.1%
The medicine should be stored out of sight and reach of children.
Store in a temperature below 25°C in a closed packaging. Protect from light.
Do not use after the expiry date stated on the packaging. The expiry date refers to the last day of the given month.
Shelf life after first opening the packaging – 30 days.
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.
6. Other information
What Rivanol 0.1% contains
- The active substance of the medicine is ethacridine lactate monohydrate. 1 g of liquid for the skin contains 1 mg of ethacridine lactate monohydrate.
- The other ingredient of the medicine is: purified water.
What Rivanol 0.1% looks like and what the packaging contains
The medicine is a yellow liquid for the skin.
Packaging available
Bottle made of orange glass with a screw cap, containing 50 g, 90 g, 100 g, 140 g, 150 g, 200 g, 250 g, 500 g, 1000 g of the medicine.
Not all packaging sizes may be available.
Marketing authorization holder
Poland
Poznańskie Zakłady Zielarskie „Herbapol” S.A.
ul. Towarowa 47-51, 61-896 Poznań
tel. +48 61 886 18 00, fax +48 61 853 60 58
Manufacturer
Poznańskie Zakłady Zielarskie „Herbapol” S.A.
Paterek, ul. Przemysłowa 3, 89-100 Nakło nad Notecią
tel. 52 386 73 10,
fax 52 386 73 23
Date of last revision of the leaflet: 06.2024
- Country of registration
- Active substance
- Prescription requiredNo
- ImporterPoznańskie Zakłady Zielarskie "Herbapol" S.A.
- This information is for reference only and does not constitute medical advice. Always consult a licensed doctor before taking any medication. Oladoctor is not responsible for medical decisions based on this content.
- Alternatives to Rivanol 0,1%Dosage form: Gel, 5 mg/g (0.5%)Active substance: ethacridine lactateManufacturer: EMO-FARM Sp. z o.o.Prescription not requiredDosage form: Aerosol, (0.10 g + 2.00 g)/100 mgActive substance: octenidine, combinationsPrescription not requiredDosage form: Cream, 50 mg/g + 5 mg/gActive substance: chlorhexidinePrescription not required
Online doctors for Rivanol 0,1%
Discuss dosage, side effects, interactions, contraindications, and prescription renewal for Rivanol 0,1% – subject to medical assessment and local rules.
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