Product image of Nurofen 24-Stunden Schmerzpflaster (Ibuprofen) supplied by GNH India

Nurofen 24-Stunden Schmerzpflaster

Active Ingredient:
Ibuprofen
Origin:
EU

Nurofen 24-Stunden Schmerzpflaster (Ibuprofen)

Ibuprofen, the active ingredient in Nurofen 24-Stunden Schmerzpflaster, is a non‑steroidal anti‑inflammatory drug presented as a topical patch for transdermal use. It provides localized pain relief and reduces inflammation for up to 24 hours in adults with musculoskeletal discomfort. GNH India supplies Nurofen 24-Stunden Schmerzpflaster as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and pharmacies worldwide.

GNH India supplies Nurofen 24-Stunden Schmerzpflaster as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and pharmacies worldwide.

Manufacturer / TM Owner

Reckitt Benckiser Deutschland Gmbh

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Indications & Clinical Uses

Nurofen 24-Stunden Schmerzpflaster contains ibuprofen, a non‑steroidal anti‑inflammatory that acts on prostaglandin synthesis in musculoskeletal tissues.

  • Musculoskeletal pain: provides up to 24 hours of localized relief for strains, sprains and minor joint aches.
  • Post‑operative pain: reduces discomfort at the surgical site when applied after minor procedures.
  • Chronic low‑back pain: helps manage persistent lumbar discomfort through continuous transdermal delivery.

How It Works

  • Ibuprofen inhibits cyclo‑oxygenase (COX‑1 and COX‑2) enzymes in peripheral tissues, decreasing the formation of prostaglandins that mediate pain, inflammation and fever. The transdermal patch delivers the drug directly to the skin, allowing local COX inhibition at the site of discomfort while limiting systemic exposure.

Side Effects

Adverse reactions to the ibuprofen patch are generally mild to moderate and reflect its anti‑inflammatory action.

Common Side Effects

  • Skin irritation at the application site: redness, itching or mild rash.
  • Localized burning sensation: transient warmth where the patch is placed.
  • Dryness of the surrounding skin: mild flaking or peeling.
  • Pruritus: itching without visible rash.

Serious or Rare Side Effects

  • Severe allergic reaction: swelling of face, lips or throat, hives, or difficulty breathing.
  • Systemic ibuprofen toxicity: gastrointestinal bleeding, ulceration or renal impairment, especially with extensive use.
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis: widespread skin detachment.
  • Anaphylaxis: rapid onset of hypotension, bronchospasm and loss of consciousness.

Precautions & Warnings

When using Nurofen 24-Stunden Schmerzpflaster, consider the following safety measures:

  • Contraindications: avoid if known allergy to ibuprofen or other NSAIDs.
  • Pregnancy: limit use; consult a healthcare professional, especially in the third trimester.
  • Renal function: assess kidney health before prolonged application.
  • Concomitant NSAIDs: do not combine with other oral or topical NSAIDs to reduce risk of toxicity.
  • Skin integrity: apply only to intact, non‑irritated skin; discontinue if severe irritation occurs.
  • Store at ambient temperature: keep below 25 °C, in the original packaging, protected from moisture and direct sunlight.

Avoid Interactions

Ibuprofen may interact with several drug classes; monitoring is advised.

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): increased risk of bleeding.
  • High‑dose aspirin: heightened gastrointestinal toxicity.
  • Selective COX‑2 inhibitors: additive renal and cardiovascular risk.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs: possible reduction in antihypertensive effect and renal function.
  • Diuretics (especially thiazides): risk of reduced renal perfusion.
  • Lithium: ibuprofen can raise serum lithium levels.
  • Methotrexate: decreased renal clearance may increase toxicity.

Frequently Asked Questions

Nurofen 24‑Stunden Schmerzpflaster is a transdermal ibuprofen patch designed to provide localized relief of musculoskeletal pain, post‑operative discomfort and chronic low‑back pain for up to 24 hours. It is applied to intact skin over the painful area and releases ibuprofen continuously to reduce inflammation and pain.

Ibuprofen blocks cyclo‑oxygenase enzymes (COX‑1 and COX‑2) in the skin and underlying tissues, lowering prostaglandin production that drives pain and inflammation. The patch delivers the drug directly to the site, allowing local COX inhibition while limiting systemic exposure.

The prescribed dosing regimen is determined by the treating clinician based on the patient’s condition, age, and overall health. The healthcare professional will decide the number of patches, application frequency and duration of therapy.

Ibuprofen should be used only if clearly needed during pregnancy, especially after the first trimester, and always under medical supervision. Breastfeeding mothers should consult a healthcare provider, as small amounts may pass into milk.

Submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any required import documentation.

The patch offers targeted, continuous delivery to the pain site, potentially reducing systemic exposure and gastrointestinal side effects compared with oral tablets. Oral ibuprofen provides systemic pain relief and is useful when widespread analgesia is required, whereas the patch is suited for localized, long‑lasting treatment.

Store the patches at ambient temperature, below 25 °C, in their original sealed packaging. Keep them away from moisture, direct sunlight and heat sources. Do not use patches that are damaged, discoloured or past their expiry date.

Clean and dry the skin area where the patch will be placed. Remove the protective liner and press the adhesive side firmly onto the skin for several seconds. Leave the patch in place for up to 24 hours, then remove and discard it safely.

Serious risks include severe allergic reactions such as anaphylaxis, systemic ibuprofen toxicity leading to gastrointestinal bleeding or renal impairment, and rare dermatological conditions like Stevens‑Johnson syndrome. Immediate medical attention is required if any of these symptoms occur.

Individuals with a known hypersensitivity to ibuprofen or other NSAIDs, those with active gastrointestinal ulcers, severe heart failure, uncontrolled hypertension, or impaired renal function should avoid using the patch. It is also contraindicated on broken or inflamed skin.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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