Product image of Lignox Spray (Lidocaine) supplied by GNH India

Lignox Spray

Active Ingredient:
Lidocaine
Origin:
EU

Lignox Spray (Lidocaine)

Lidocaine, the active ingredient in Lignox Spray, is a local anesthetic presented as a spray for cutaneous or oromucosal use. It provides temporary numbing of surface tissues and is used to relieve pain associated with minor skin injuries, oral lesions, and minor procedural preparations.

GNH India supplies Lignox Spray as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Chema Elektromet Spoldzielnia Pracy

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Indications & Clinical Uses

  • Lignox Spray contains lidocaine, a local anesthetic that acts on peripheral nerve sodium channels to provide surface analgesia.
  • Minor skin abrasions, burns, or insect bites: provides temporary numbing and reduces pain during daily activities.
  • Aphthous ulcers and other oral mucosal lesions: eases discomfort and facilitates eating or speaking.
  • Pre‑procedural topical anesthesia for minor dermatologic or dental procedures: numbs the targeted area to improve patient tolerance.

How It Works

  • Lidocaine reversibly blocks voltage‑gated sodium channels on neuronal membranes, preventing the initiation and propagation of nerve impulses. By stabilizing the neuronal membrane, it inhibits depolarization and reduces the transmission of pain signals from the peripheral site to the central nervous system, resulting in localized loss of sensation.

Side Effects

Lignox Spray may cause local or systemic adverse reactions, most of which are mild and transient.

Common Side Effects

  • Transient burning or stinging sensation at the application site
  • Mild itching or erythema of the skin or mucosa
  • Temporary tingling or numbness beyond the treated area

Serious or Rare Side Effects

  • Allergic reactions such as angioedema, urticaria, or anaphylaxis
  • Systemic toxicity presenting as dizziness, seizures, or cardiac arrhythmias
  • Rare methemoglobinemia, especially with extensive mucosal use

Precautions & Warnings

  • When using Lignox Spray, consider the following safety measures.
  • Allergy assessment: avoid if known hypersensitivity to lidocaine or other amide‑type anesthetics.
  • Application area: limit to intact skin or mucosa; do not apply to open wounds or heavily damaged tissue.
  • Dosage limit: do not exceed the total recommended amount per treatment session as advised by the prescriber.
  • Concurrent anesthetics: avoid using multiple lidocaine‑containing products simultaneously to prevent cumulative toxicity.
  • Pregnancy and lactation: use only if the potential benefit justifies the potential risk to the fetus or infant.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Lignox Spray may interact with other medications; consider the following.

Major Interactions (Avoid)

  • Class I antiarrhythmic agents (e.g., quinidine, procainamide): may increase systemic lidocaine concentrations.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole, erythromycin): can raise lidocaine levels and risk toxicity.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may enhance cardiac depressant effects of lidocaine.
  • Concurrent use of other local anesthetics: increases risk of cumulative systemic toxicity.
  • Epinephrine‑containing products: may alter lidocaine absorption and prolong its action.

Frequently Asked Questions

Lignox Spray is a lidocaine‑based topical formulation used to provide temporary numbness and pain relief on the skin or oral mucosa. It is commonly applied to minor abrasions, burns, insect bites, aphthous ulcers, and before minor dermatologic or dental procedures to improve patient comfort.

Lidocaine works by reversibly blocking voltage‑gated sodium channels on peripheral nerves. This inhibition prevents the initiation and propagation of nerve impulses, thereby reducing the transmission of pain signals from the site of application to the brain and producing localized anesthesia.

The appropriate amount of Lignox Spray is determined by the prescribing healthcare professional based on the size of the area to be treated and the specific clinical situation. Patients should follow the prescriber’s instructions and not exceed the recommended total amount per session.

Safety data for lidocaine spray in pregnancy and lactation are limited. It should be used only if the potential benefit to the mother outweighs any possible risk to the fetus or infant. Healthcare providers should evaluate each case individually before prescribing.

To request Lignox Spray, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, and will verify trade or institutional credentials before providing pricing, availability, shipping details and any necessary import documentation.

Lignox Spray delivers lidocaine, an amide‑type local anesthetic, which offers rapid onset and reliable surface numbness. Compared with ester‑type anesthetics such as benzocaine, lidocaine generally has a lower risk of allergic reactions and provides a longer duration of action, making it suitable for a broader range of minor procedures.

Lignox Spray should be stored at room temperature, below 25 °C, in its original container. Keep the product away from moisture, direct sunlight, and sources of heat. Ensure the spray nozzle is clean and capped when not in use to maintain product integrity.

Lignox Spray is applied directly to the target skin or oral mucosal area as a fine mist. The prescribed amount is sprayed onto the surface, allowing it to spread evenly. The spray should be used on intact tissue, and the treated area is typically left uncovered to allow absorption.

Serious risks include systemic lidocaine toxicity, which can manifest as dizziness, seizures, or cardiac arrhythmias, and severe allergic reactions such as angioedema or anaphylaxis. Rarely, extensive mucosal use may lead to methemoglobinemia. Any signs of systemic effects or allergic response require immediate medical attention.

Individuals with a known hypersensitivity to lidocaine, other amide‑type local anesthetics, or any component of the spray formulation should avoid its use. It is also contraindicated on broken skin, heavily damaged mucosa, or in patients where the prescriber determines that the risks outweigh the benefits.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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