Product image of Nicorette Invisipatch (Nicotine) supplied by GNH India

Nicorette Invisipatch

Active Ingredient:
Nicotine
Origin:
EU

Nicorette Invisipatch (Nicotine)

Nicotine, the active ingredient in Nicorette Invisipatch, is a nicotinic agonist presented as a transdermal patch for transdermal use. It is indicated for adult smokers seeking to quit by providing a controlled release of nicotine to alleviate withdrawal symptoms and cravings, supporting a gradual reduction in tobacco dependence.

GNH India supplies Nicorette Invisipatch as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring consistent quality and regulatory compliance across markets.

Manufacturer / TM Owner

Mcneil Ab

1
Pack/s
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Indications & Clinical Uses

Nicorette Invisipatch, a nicotine replacement therapy, is used in smoking cessation.

  • Smoking cessation: helps adult smokers reduce withdrawal symptoms and gradually discontinue tobacco use.
  • Tobacco dependence: provides a steady nicotine dose to support quitting efforts.
  • Relapse prevention: assists recent quitters in maintaining abstinence from cigarettes.

How It Works

  • Nicotine delivered through the transdermal matrix of the Invisipatch enters systemic circulation and binds to nicotinic acetylcholine receptors in the central nervous system. This stimulation reduces the intensity of nicotine withdrawal and cravings, allowing a gradual tapering of nicotine exposure while mimicking the pharmacokinetic profile of smoked tobacco.

Side Effects

Common Side Effects

  • Skin irritation at the application site: redness, itching, or mild rash.
  • Sleep disturbance: insomnia or vivid dreams.
  • Nausea: mild stomach upset.
  • Headache: transient tension-type headache.
  • Dizziness: light‑headed feeling.
  • Mouth irritation: tingling or dryness.

Serious or Rare Side Effects

  • Severe allergic reaction: swelling, hives, or difficulty breathing.
  • Extensive skin rash: blistering or severe dermatitis.
  • Cardiovascular events: chest pain, palpitations, or hypertension.
  • Hypotension: marked drop in blood pressure.
  • Arrhythmia: irregular heart rhythm.
  • Severe dizziness or fainting.

Precautions & Warnings

Before using Nicorette Invisipatch, consider the following precautions:

  • Assess nicotine dependence level: determine appropriate patch strength.
  • Avoid use in non‑smokers or occasional smokers: unnecessary nicotine exposure.
  • Do not apply to damaged or irritated skin: may increase irritation.
  • Do not combine with other nicotine replacement products: risk of nicotine overdose.
  • Monitor cardiovascular status: patients with heart disease should use under medical supervision.
  • Store at room temperature: keep in the original pouch, protect from moisture and direct heat.

Avoid Interactions

Nicorette Invisipatch may interact with other medicines. Review the following groups:

Major Interactions (Avoid)

  • Monoamine oxidase inhibitors (MAOIs): may amplify nicotine’s cardiovascular effects.
  • CYP2A6 inhibitors (e.g., methoxsalen): can raise systemic nicotine levels.
  • Insulin or oral hypoglycemics: nicotine may affect glucose control.

Moderate Interactions (Monitor Closely)

  • Antidepressants (SSRIs, SNRIs): monitor for increased side‑effects such as insomnia.
  • Beta‑blockers: nicotine‑induced tachycardia may be masked.
  • Theophylline: nicotine can alter plasma concentrations, requiring dose adjustment.

Frequently Asked Questions

Nicorette Invisipatch is an over‑the‑counter nicotine replacement product designed to help adult smokers quit by delivering a steady dose of nicotine through the skin, reducing cravings and withdrawal symptoms during a quit attempt.

The patch releases nicotine that is absorbed transdermally into the bloodstream, where it binds to nicotinic acetylcholine receptors in the brain. This mimics the effect of cigarette‑derived nicotine, easing withdrawal while allowing a gradual reduction in nicotine exposure.

The appropriate patch strength and duration are determined by the prescribing clinician based on the individual’s smoking history, level of dependence, and previous quit attempts. The prescriber selects the regimen that best supports a step‑down approach.

Safety data for nicotine patches in pregnancy and lactation are limited. Women who are pregnant, planning pregnancy, or breastfeeding should discuss potential risks and alternatives with their healthcare provider before using the product.

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 necessary import documentation.

Compared with gum or lozenges, the patch offers a once‑daily, steady nicotine delivery, which can improve adherence and reduce the need for frequent dosing. It avoids oral irritation but may cause skin reactions, whereas other forms may cause gastrointestinal side effects.

Store the patches at room temperature, below 25 °C, in the original sealed pouch. Keep them away from moisture, direct sunlight and heat sources to maintain adhesive integrity and nicotine stability.

The patch is applied to a clean, dry, hair‑free area of the upper body or upper arm. Press firmly for several seconds, then replace the patch according to the prescriber’s schedule, typically every 24 hours, rotating sites to minimize skin irritation.

Serious risks include severe allergic reactions, extensive skin rash, cardiovascular events such as chest pain or arrhythmia, and significant hypotension. Users should seek immediate medical attention if any of these symptoms occur.

The patch should not be used by non‑smokers, occasional smokers, individuals with known hypersensitivity to nicotine or patch components, or patients with severe uncontrolled cardiovascular disease without medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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