Nurofen® 24-hour pain plaster is a plaster containing 200 mg ibuprofen per plaster (medicinal product). For the short-term, symptomatic treatment of localised pain in acute muscle strains or blunt trauma.
€17.95*
Prices incl. VAT plus shipping costs (Kann sich je nach Land ändern)
⁴
Nurofen® 24-hour pain patch is a patch containing 200 mg ibuprofen per patch (medicinal product).
The active ingredient is ibuprofen. Ibuprofen belongs to a group of medicines known as non-steroidal anti-inflammatory drugs (NSAIDs). These medicines influence the body's response to pain, swelling and increased temperature. The patch containing the active ingredient continuously releases ibuprofen at the painful site during the 24 hours of application.
Nurofen 24-hour pain plasters are used in adults and adolescents aged 16 and over for the short-term, symptomatic treatment
- localised pain in acute muscle strains
- sprained limbs near the joints following blunt trauma.
Effective and long-lasting pain relief!
Acute pain in the musculoskeletal system such as muscle, joint or shoulder and neck pain due to strains or sprains: The new Nurofen 24-hour pain plaster 200 mg provides effective and long-lasting pain relief. Its unique fabric structure ensures the continuous release of the proven active ingredient ibuprofen, so that the pain-relieving effect lasts around the clock.
The plaster is applied directly to the painful area and is very comfortable and inconspicuous to wear thanks to its ultra-flexibility. Thanks to effective pain relief, nothing stands in the way of everyday activities - whether at work, gardening, hiking with friends or playing with the grandchildren. Thanks to the localised absorption of the active ingredient, the Nurofen 24-hour pain plaster hardly affects other areas of the body, such as the stomach. The plaster is proven to be well tolerated. Daily application is sufficient for adults and adolescents.
Product advantages of Nurofen® 24-hour pain plasters
- Use once a day, without creams or tablets
- Apply directly to the painful area, so the pain plaster can work exactly where it hurts
- The 10 cm x 14 cm plaster impresses with its strong hold in difficult areas, such as joints or the shoulder area
- At just 0.64 mm, it is wafer-thin and ultra-flexible
Dosage form
plaster
Application
- Adults and adolescents aged 16 and over: One dose corresponds to one patch containing the active ingredient. The maximum dose within 24 hours is one patch containing the active ingredient.
- Children and adolescents under 16 years of age: Do not use this medicine in children and adolescents under 16 years of age.
- Duration of use: To relieve your symptoms, apply as few patches containing the active ingredient as necessary over the shortest possible period of time. Do not use this medicine for more than 5 days. If symptoms persist for more than 5 days, seek medical advice.
Route of administration: For use on intact skin.
Carefully clean and dry the area to be treated before applying the plaster. The plaster can be applied at any time during the day or night, but must be replaced with a new plaster at the same time the next day. The plaster containing the active ingredient is flexible and adaptable. If necessary, the plaster can be applied on or next to a joint and it will allow normal movement.
The plaster:
- Do not cut. It must be applied as a whole;
- Do not apply to injured or diseased skin;
- Do not cover with another plaster or with impermeable clothing or bandages;
- Do not allow to get wet.
Method of application:
- Tear or cut open the pouch along the dotted line and remove a plaster containing the active ingredient.
- Remove the protective film marked (A) and then apply the plaster to the centre of the painful area.
- Remove the protective film labelled (B), stretch the plaster slightly and smooth this part of the plaster onto the skin.
- Remove the protective film labelled (C).
- Stretch the plaster slightly and smooth the rest of the plaster over the skin.
Ingredients
- Each active ingredient-containing plaster contains 200 mg ibuprofen.
- Other ingredients: Adhesive layer: Macrogol 20000, Macrogol 400, Levomenthol, Polystyrene-block-polyisoprene-block-polystyrene (11 : 78 : 11), Polyisobutylene, Hydrogenated rosin glycerol esters, Viscous paraffin Carrier layer: Poly(ethylene terephthalate), woven Peelable protective film Poly(ethylene terephthalate), siliconised
| Größe: | Keine Angabe |
|---|---|
| Alkoholfrei: | Keine Angabe |
| Diabetiker: | Keine Angabe |
| Farbe: | Keine Angabe |
| Fruktosefrei: | Keine Angabe |
| Geschmack: | Keine Angabe |
| Glutenfrei: | Keine Angabe |
| Laktosefrei: | Keine Angabe |
| Nahrungsergänzung: | Keine Angabe |
| Parfum: | Keine Angabe |
| Vegan: | Keine Angabe |
| Vegetarier: | Keine Angabe |
| Zuckerfrei: | Keine Angabe |
| Stück: | 4 |
Anwendungshinweise
| Art der Anwendung: | LogImport.sisx.AAD.Auf schmerzende Hautpartie kleben Nur auf intakter Haut anwenden Pflaster nicht teilen und nicht unter einem Okklusivverband anwenden |
|---|---|
| Anwendungsgebiet: | LogImport.sisx.AGD.Kurzzeitig bei lokalen Schmerzen bei akuten Muskelzerrungen, verstauchten Gliedmaßen nach stumpfem Trauma |
| Dosierung: | LogImport.sisx.DOD.Personen ab 16 Jahren 1mal tgl 1 Pflaster Nach 24 Std Pflaster wechseln Max Behandlungsdauer 5 Tage Nicht für Kinder und Jugendliche unter 16 Jahren |
| Eigenschaften und Wirksamkeit: | LogImport.sisx.EWD.Nichtsteroidales Antiphlogistikum |
| Gegenanzeigen: | LogImport.sisx.GAD.Analgetika-Überempfindlichkeit Nicht auf verletzter oder beschädigter Haut, an Augen, Lippen oder Schleimhäuten anwenden |
| Nebenwirkungen: | LogImport.sisx.NWD.Lokale Reaktionen, Überempfindlichkeit, schwere Hautreaktionen, Dyspepsie, Niere |
| Besondere Warnhinweise zur sicheren Anwendung: | LogImport.sisx.WHD.Nicht auf verletzter oder beschädigter Haut, an Augen, Lippen oder Schleimhäuten anwenden Bei Hautausschlag Pflaster sofort entfernen An der behandelten Stelle Sonnnenlicht oder UV- Strahlung vermeiden |
| Wechselwirkungen: | LogImport.sisx.WWD.Bei topischer Anwendung Wahrscheinlichkeit für WW gering |
| Schwangerschaft und Stillperiode: | LogImport.sisx.SSTD.Zwingende Indikationsstellung in 1 und 2 Trimenon, Gegenanzeige im 3Trimenon Stillen möglich, aber Pflaster nicht auf der Brust aufbringen |
Schwangerschaftshinweise
| Anwendung verboten |
|---|
| Anwendung nur bei zwingender oder vitaler Indikation |
Stillzeithinweise
| Stillen erlaubt |
|---|
| Stillen unter sorgfältiger Kontrolle möglich |
Piktogramme
| Vorsicht Photosensibilität, übermäßige UV-Strahlung meiden |
|---|