Product image of Metoxsalene S.A.L.F. (Methoxsalen) supplied by GNH India

Metoxsalene S.A.L.F.

Active Ingredient:
Methoxsalen
Origin:
EU

Metoxsalene S.A.L.F. (Methoxsalen)

Methoxsalen, the active ingredient in Metoxsalene S.A.L.F., is a psoralen presented as a sterile solution for extracorporeal use. It is employed in PUVA therapy to treat chronic skin disorders such as psoriasis and vitiligo in adult patients.

GNH India supplies Metoxsalene S.A.L.F. as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

S.A.L.F. Spa Laboratorio Farmacologico

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Indications & Clinical Uses

Methoxsalen is used in dermatologic conditions that respond to PUVA therapy, targeting abnormal skin cell proliferation and depigmentation.

  • Psoriasis: reduces scaling, erythema and plaque thickness.
  • Vitiligo: promotes repigmentation of depigmented patches.
  • Cutaneous T‑cell lymphoma: used as part of PUVA protocols to control skin lesions.

How It Works

  • Methoxsalen intercalates into DNA strands and, upon activation by UVA light during PUVA therapy, forms covalent cross‑links between DNA bases. These cross‑links inhibit DNA synthesis and cell division, leading to reduced proliferation of hyperactive keratinocytes and melanocytes, thereby normalizing skin appearance.

Side Effects

Methoxsalen may cause a range of adverse reactions, from mild to severe, depending on exposure and patient factors.

Common Side Effects

  • Nausea: transient gastrointestinal upset after administration.
  • Headache: mild to moderate intensity during treatment.
  • Erythema: redness of skin at treated sites.
  • Itching: pruritus associated with phototoxic reaction.
  • Hyperpigmentation: darkening of exposed skin areas.
  • Phototoxicity: heightened skin sensitivity to UVA.

Serious or Rare Side Effects

  • Severe burns: deep skin injury from excessive UVA exposure.
  • Blistering: formation of fluid‑filled lesions on irradiated skin.
  • Cutaneous malignancies: increased risk of skin cancer with long‑term use.
  • Ocular cataracts: lens opacity from systemic exposure.
  • Hemolysis in G6PD deficiency: rapid destruction of red blood cells.
  • Systemic hypersensitivity: rare allergic reactions requiring medical attention.

Precautions & Warnings

Methoxsalen requires careful patient assessment and monitoring to minimize risks.

  • Assess skin type: evaluate for high phototype or history of skin cancer.
  • Avoid excessive UVA: limit exposure time and intensity during PUVA sessions.
  • Monitor ocular health: schedule regular eye examinations for cataract detection.
  • Check G6PD status: contraindicated in patients with glucose‑6‑phosphate dehydrogenase deficiency.
  • Store at ambient temperature: keep below 25°C, in original packaging, protected from moisture and light.

Avoid Interactions

Methoxsalen can interact with other agents that influence photosensitivity or coagulation.

Major Interactions (Avoid)

  • Azathioprine: additive immunosuppression may increase infection risk.
  • Cyclosporine: combined phototoxic effects can exacerbate skin damage.
  • Retinoids (e.g., acitretin): heightened photosensitivity and mucocutaneous toxicity.

Moderate Interactions (Monitor Closely)

  • Oral contraceptives: possible reduction in efficacy due to hepatic enzyme induction.
  • Antifungal azoles (e.g., ketoconazole): may alter methoxsalen metabolism.
  • Anticoagulants (e.g., warfarin): monitor INR as phototherapy can affect vitamin K levels.

Frequently Asked Questions

Metoxsalene S.A.L.F. contains methoxsalen, a psoralen used in PUVA therapy to treat chronic skin disorders such as psoriasis, vitiligo and certain types of cutaneous T‑cell lymphoma by reducing abnormal cell growth and promoting repigmentation.

Methoxsalen intercalates into DNA and, when activated by UVA light, creates covalent cross‑links between DNA strands. This blocks DNA replication and cell division, leading to decreased proliferation of hyperactive skin cells and facilitating therapeutic effects in PUVA treatment.

The dosage of Metoxsalene S.A.L.F. is determined by the prescribing physician based on the patient’s condition, skin type, and response to PUVA therapy. Only a qualified healthcare professional should set the appropriate regimen.

Safety data for methoxsalen in pregnancy and lactation are limited. It is generally advised to avoid use unless the potential benefit justifies the potential risk, and the decision should be made by a qualified healthcare provider.

To order, 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.

Metoxsalene S.A.L.F. provides methoxsalen of EU‑grade quality for PUVA therapy, comparable in efficacy to other licensed methoxsalen preparations. Differences may lie in manufacturing standards, packaging and supply chain reliability, where GNH India emphasizes GDP compliance and global distribution.

Store at ambient temperature below 25 °C. Keep the product in its original container, protect it from moisture and direct light, and ensure the seal remains intact until use.

Metoxsalene S.A.L.F. is supplied as a sterile solution for extracorporeal use. It is applied to the patient’s skin or mucous membranes before exposure to a controlled dose of UVA light in a clinical PUVA setting, following the protocol set by the treating physician.

Serious risks include severe phototoxic burns, blistering, increased long‑term risk of cutaneous malignancies, ocular cataracts, and hemolysis in patients with G6PD deficiency. Patients should be monitored closely for these events during and after treatment.

Metoxsalene S.A.L.F. should be avoided in patients with known hypersensitivity to methoxsalen or other psoralens, those with active skin cancers, severe liver disease, G6PD deficiency, or in individuals who cannot safely undergo controlled UVA exposure.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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