Product image of Infloc (Sodium Fusidate) supplied by GNH India

Infloc

Active Ingredient:
Sodium Fusidate
Origin:
EU

Infloc (Sodium Fusidate)

Sodium fusidate, the active ingredient in Infloc, is a fusidic acid antibiotic presented as a topical formulation for cutaneous use. It treats skin infections such as impetigo, folliculitis and secondary bacterial infections of dermatitis in patients requiring topical therapy.

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

Manufacturer / TM Owner

Noreva Portugal - Unipessoal, Lda

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Indications & Clinical Uses

Infloc, a fusidic acid antibiotic, is applied to bacterial skin infections.

  • Impetigo: reduces bacterial load and promotes healing of superficial skin lesions.
  • Folliculitis: eliminates the causative Staphylococcus organisms and alleviates inflammation.
  • Secondary bacterial infections of dermatitis: controls bacterial overgrowth and prevents worsening of dermatitis lesions.

How It Works

  • Sodium fusidate inhibits bacterial protein synthesis by binding to elongation factor G (EF‑G) on the ribosome, preventing its turnover and blocking the translocation step of peptide chain elongation, which halts bacterial growth.

Side Effects

Adverse reactions may occur with topical use of Infloc.

Common Side Effects

  • Skin irritation: mild redness or discomfort at the application site.
  • Itching: localized pruritus.
  • Burning sensation: transient warmth or stinging.
  • Dryness: flaking or scaling of the skin.
  • Rash: erythematous macular eruption.
  • Contact dermatitis: localized allergic response.

Serious or Rare Side Effects

  • Allergic reaction: swelling, hives, or angioedema.
  • Stevens‑Johnson syndrome: severe mucocutaneous necrosis.
  • Toxic epidermal necrolysis: extensive skin detachment.
  • Severe dermatitis: widespread inflammation.
  • Systemic hypersensitivity: fever, malaise, or organ involvement.
  • Anaphylaxis: rapid onset of life‑threatening symptoms.

Precautions & Warnings

When using Infloc, consider the following safety measures.

  • Allergy assessment: verify no known hypersensitivity to fusidic acid or formulation components.
  • Indication limitation: apply only to the specified skin infections.
  • Surface area restriction: avoid extensive application over large body areas.
  • Monitoring: watch for signs of worsening infection or systemic absorption, especially on compromised skin.
  • Avoid ocular use: do not apply to eyes or mucous membranes.
  • Store at room temperature: keep in the original packaging, protect from moisture and light.

Avoid Interactions

Potential drug interactions should be evaluated before prescribing Infloc.

Major Interactions (Avoid)

  • Concurrent systemic fusidic acid: may increase systemic exposure.
  • Topical corticosteroids: can mask infection signs and reduce efficacy.
  • Other topical antibiotics: possible antagonistic effects.

Moderate Interactions (Monitor Closely)

  • Silver‑containing dressings: may affect drug absorption.
  • Moisturizers or emollients: could dilute the concentration.
  • Phototherapy: may increase photosensitivity risk.

Frequently Asked Questions

Infloc contains sodium fusidate and is indicated for the topical treatment of bacterial skin infections such as impetigo, folliculitis, and secondary bacterial infections that complicate dermatitis. It is applied directly to the affected skin to reduce bacterial load and promote healing.

Sodium fusidate acts by binding to the bacterial elongation factor G (EF‑G) on the ribosome, preventing its release and blocking the translocation step of protein synthesis. This inhibition halts bacterial growth, allowing the immune system to clear the infection.

The dosage of Infloc is determined by the prescribing healthcare professional based on the type and severity of the skin infection, the patient’s age, and the area of skin involved. The prescriber will specify the amount to apply and frequency of use.

Safety data for sodium fusidate in pregnancy and lactation are limited. Healthcare providers should weigh the potential benefits against any possible risks before prescribing Infloc to pregnant or breastfeeding individuals.

To order Infloc, submit an enquiry on the product page at gnhindia.com, indicating 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.

Infloc’s active ingredient, sodium fusidate, offers a unique mechanism by targeting EF‑G, which differs from many other topical antibiotics that inhibit cell wall synthesis. This can be advantageous in infections caused by fusidic‑acid‑sensitive strains, though susceptibility testing is recommended.

Store Infloc at room temperature, below 25 °C. Keep the product in its original packaging, protect it from moisture and direct sunlight, and ensure the container is tightly closed when not in use.

Infloc is applied topically to the affected skin area. The prescriber will advise the amount to spread, usually a thin layer, and the frequency—commonly two to three times daily—until the infection resolves.

Serious risks include severe allergic reactions such as anaphylaxis, Stevens‑Johnson syndrome, and toxic epidermal necrolysis. Patients should discontinue use and seek immediate medical attention if they develop widespread rash, blistering, or systemic symptoms.

Infloc should not be used by individuals with a known hypersensitivity to sodium fusidate or any excipients in the formulation. It is also contraindicated on the eyes, mucous membranes, and on extensive damaged skin without medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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