Product image of Oftasteril Alfa Intes (Povidone, Iodinated) supplied by GNH India

Oftasteril Alfa Intes

Active Ingredient:
Povidone, Iodinated
Origin:
EU

Oftasteril Alfa Intes (Povidone, Iodinated)

Povidone‑iodine, the active ingredient in Oftasteril Alfa Intes, is an antiseptic, disinfectant presented as a solution for ocular use. It reduces microbial contamination on the eye surface and is employed before and after eye procedures and in minor eye injuries.
GNH India supplies Oftasteril Alfa Intes as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Alfa Intes Industria Terapeutica Splendore Via Fratelli

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Indications & Clinical Uses

  • Oftasteril Alfa Intes, a povidone‑iodine ophthalmic antiseptic, provides antimicrobial protection for the eye in several clinical situations.
  • Ocular surface antisepsis: reduces microbial load prior to examinations or procedures.
  • Pre‑ and post‑operative eye preparation: helps prevent surgical site infection.
  • Minor eye injuries: minimizes risk of infection in superficial trauma.

How It Works

  • Povidone‑iodine releases free iodine when applied to the ocular surface. The iodine penetrates microbial cell walls, oxidizes cellular components and denatures proteins, leading to rapid microbial death across a broad spectrum of bacteria, viruses, fungi and protozoa.

Side Effects

Adverse reactions may occur following ocular application of povidone‑iodine.

Common Side Effects

  • Stinging or burning sensation at the site of application.
  • Redness of the conjunctiva or eyelid margin.
  • Excessive tearing or watery discharge.
  • Transient blurred vision.
  • Mild allergic contact dermatitis of the peri‑ocular skin.
  • Temporary irritation of the corneal epithelium.

Serious or Rare Side Effects

  • Anaphylactic reaction or severe systemic allergy.
  • Corneal ulceration or persistent keratitis.
  • Severe pain or photophobia.
  • Vision loss due to ocular toxicity.
  • Significant intra‑ocular inflammation.

Precautions & Warnings

Use of povidone‑iodine ophthalmic preparations requires careful consideration of patient factors and handling.

  • Allergy assessment: avoid in individuals with known iodine or povidone‑iodine hypersensitivity.
  • Pregnancy and lactation: limit use to situations where benefit outweighs potential risk, as safety data are limited.
  • Contact lens wearers: remove lenses before application and wait before reinserting.
  • Duration of use: limit to the shortest period necessary to achieve antisepsis.
  • Eye condition: avoid in patients with active corneal epithelial defects unless directed by a specialist.
  • Store at ambient temperature: keep in original container, protect from light and moisture.

Avoid Interactions

Povidone‑iodine may interact with other agents that affect iodine balance or ocular tolerance.

Major Interactions (Avoid)

  • Thyroid hormone therapy (levothyroxine): excess iodine may interfere with absorption.
  • Antithyroid medications (e.g., propylthiouracil): iodine load may reduce drug efficacy.

Moderate Interactions (Monitor Closely)

  • Concurrent use of other ocular antiseptics: may increase local irritation.
  • Preservative‑containing contact lens solutions: additive toxicity possible.
  • Systemic iodine supplements: may raise total iodine exposure.

Frequently Asked Questions

Oftasteril Alfa Intes is an ophthalmic antiseptic containing povidone‑iodine. It is applied to the eye to reduce microbial contamination before and after surgical procedures, during routine examinations, and in minor eye injuries to help prevent infection.

Povidone‑iodine releases free iodine when it contacts the ocular surface. The iodine penetrates the cell walls of microorganisms, oxidizes essential proteins and nucleic acids, and causes rapid cell death, providing broad‑spectrum antimicrobial activity.

The dose and frequency of Oftasteril Alfa Intes are determined by the prescribing clinician based on the specific procedure or condition. No fixed regimen is provided publicly; the healthcare professional will specify the appropriate amount and timing.

Safety data for povidone‑iodine ophthalmic use during pregnancy and lactation are limited. It should be used only if clearly needed and after a risk‑benefit assessment by the treating physician.

To order, submit an enquiry on the product page at gnhindia.com with 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 alternatives such as chlorhexidine eye solutions, povidone‑iodine offers a broader antimicrobial spectrum, including viruses and spores. It is inexpensive and widely available, but may cause more ocular irritation than some newer agents. Choice depends on clinical need, tolerance and institutional protocols.

Store the product at ambient temperature, preferably below 25 °C, in its original sealed container. Protect it from direct sunlight, excessive heat and moisture to maintain stability and efficacy.

The solution is instilled directly onto the ocular surface, typically as one or more drops, according to the prescriber's instructions. The eye should be closed gently for a few seconds to allow contact, and contact lenses should be removed before application.

Serious risks include severe allergic reactions such as anaphylaxis, corneal ulceration or persistent keratitis, and potential vision loss if toxicity occurs. Immediate medical attention is required if any of these symptoms develop.

Individuals with a known allergy to iodine or povidone‑iodine, patients with uncontrolled thyroid disease, and those with active corneal epithelial defects or severe ocular surface disease should avoid using this product unless directed by a specialist.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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