Product image of Nicotinell Lakrits (Nicotine Polacrilex) supplied by GNH India

Nicotinell Lakrits

Active Ingredient:
Nicotine Polacrilex
Origin:
EU

Nicotinell Lakrits (Nicotine Polacrilex)

Nicotine Polacrilex, the active ingredient in Nicotinell Lakrits, is a nicotine replacement therapy presented as a buccal delivery system for buccal use. It is available over‑the‑counter and provides controlled nicotine to adults seeking to quit smoking, helping to reduce withdrawal symptoms and cravings.

GNH India supplies Nicotinell Lakrits as a licensed, GDP‑compliant international pharmaceutical supplier, adhering to EU GMP standards and providing the product to pharmacies, hospitals and clinics worldwide through a regulated distribution network, ensuring timely delivery and compliance with local regulations.

Manufacturer / TM Owner

Reddy Holding Gmbh

1
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Indications & Clinical Uses

Nicotinell Lakrits, a nicotine replacement therapy, is used in the management of nicotine dependence during smoking cessation.

  • Smoking cessation: assists adult smokers in reducing cravings and withdrawal symptoms when quitting tobacco.
  • Tobacco dependence: provides a controlled nicotine dose to replace cigarettes and support gradual reduction.
  • Relapse prevention: helps maintain abstinence by delivering nicotine without the harmful smoke constituents.

How It Works

  • Nicotine Polacrilex is a resin‑bound nicotine complex that releases nicotine slowly when placed in the buccal cavity. The nicotine is absorbed through the oral mucosa into the bloodstream, where it binds to nicotinic acetylcholine receptors in the central nervous system, partially stimulating the same pathways activated by cigarette smoke and thereby diminishing withdrawal and craving intensity.

Side Effects

Nicotinell Lakrits may cause a range of adverse reactions, most of which are mild and transient.

Common Side Effects

  • Mouth irritation: mild soreness or tingling in the oral cavity.
  • Hiccups: transient episodes after placement.
  • Nausea: occasional feeling of queasiness.
  • Headache: mild to moderate intensity.
  • Dizziness: brief light‑headedness.
  • Increased salivation: excess saliva production.

Serious or Rare Side Effects

  • Severe allergic reaction: signs include rash, swelling, or anaphylaxis.
  • Chest pain or palpitations: may indicate cardiovascular stress.
  • Arrhythmia or hypertension: abnormal heart rhythm or elevated blood pressure.
  • Oral ulceration: painful sores in the mouth.
  • Persistent vomiting: prolonged nausea and vomiting.

Precautions & Warnings

Before using Nicotinell Lakrits, consider the following precautions.

  • Assess nicotine dependence level: evaluate the patient’s smoking history before initiating therapy.
  • Avoid use in children and adolescents: product is not indicated for persons under 18 years.
  • Do not use if allergic to nicotine or excipients: discontinue immediately if hypersensitivity occurs.
  • Monitor cardiovascular status: patients with recent heart attack or uncontrolled hypertension should use under medical supervision.
  • Limit duration of use: typically not exceeding 12 weeks without professional review.
  • Store at ambient temperature: keep below 25 °C, in original packaging, protected from moisture and direct sunlight.

Avoid Interactions

Nicotinell Lakrits can interact with other medicines; review the following.

Major Interactions (Avoid)

  • Monoamine oxidase inhibitors (MAOIs): may increase risk of hypertensive crisis.
  • Other nicotine replacement products: risk of nicotine overdose.
  • CYP2A6 inhibitors (e.g., methoxsalen): may increase nicotine levels.

Moderate Interactions (Monitor Closely)

  • Antidepressants (SSRIs, SNRIs): may augment nicotine’s effect on mood; monitor for side effects.
  • Beta‑blockers: nicotine may reduce their efficacy; observe blood pressure.
  • Theophylline: nicotine may increase metabolism, requiring dose adjustment if needed.

Frequently Asked Questions

Nicotinell Lakrits is an over‑the‑counter nicotine replacement product used to help adult smokers quit by reducing cravings and withdrawal symptoms associated with nicotine dependence.

Nicotine polacrilex is a resin‑bound nicotine complex that releases nicotine slowly in the mouth. The nicotine is absorbed through the buccal mucosa, reaches the bloodstream and activates nicotinic acetylcholine receptors in the brain, mimicking the effect of cigarette smoke and easing withdrawal.

The specific dose and duration are determined by the prescribing healthcare professional based on the individual’s smoking history, level of dependence, and response to therapy. Patients should follow the prescriber’s instructions and not exceed the recommended amount.

Safety data for nicotine polacrilex in pregnancy and lactation are limited. Women who are pregnant, planning to become pregnant, or breastfeeding should discuss potential risks and benefits with their healthcare provider before using this product.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies 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 nicotine patches, gum or lozenges, Nicotinell Lakrits delivers nicotine via buccal absorption, offering rapid onset and flexible dosing. It may be preferred by users who dislike the adhesive patch or who want a discreet, chew‑free option, while still providing comparable efficacy in reducing cravings.

Store the product at ambient temperature, preferably below 25 °C, in its original packaging. Protect it from moisture, direct sunlight and extreme heat. Keep out of reach of children and do not use if the package is damaged.

Place the tablet or lozenge between the gum and cheek, allowing it to dissolve slowly. Do not chew or swallow whole. Keep the product in place for the recommended time, usually several minutes, to ensure optimal buccal absorption of nicotine.

Serious adverse reactions, although rare, include severe allergic responses such as anaphylaxis, chest pain or palpitations, arrhythmias, hypertension, and oral ulceration. Users should seek immediate medical attention if any of these symptoms occur.

The product should not be used by individuals under 18 years of age, persons with known hypersensitivity to nicotine or any excipients, and patients with recent myocardial infarction, uncontrolled hypertension, or severe cardiovascular disease without medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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