Product image of Linoladiol-H N (Estradiol Hemihydrate, Prednisolone Sesquihydrate) supplied by GNH India

Linoladiol-H N

Active Ingredient:
Estradiol Hemihydrate, Prednisolone Sesquihydrate
Origin:
EU

Linoladiol-H N (Estradiol Hemihydrate, Prednisolone Sesquihydrate)

Estradiol hemihydrate and prednisolone sesquihydrate, the active ingredients in Linoladiol-H N, are an estrogen and a corticosteroid presented as a topical formulation for skin application. It treats estrogen deficiency and inflammatory skin conditions in adult women.

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

Manufacturer / TM Owner

Dr. August Wolff Gmbh & Co. Kg Arzneimittel

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Indications & Clinical Uses

  • Linoladiol-H N combines an estrogen and a corticosteroid and is used in therapeutic areas that involve hormonal regulation and inflammation.
  • Menopausal estrogen deficiency: provides localized estrogen to relieve urogenital atrophy and dryness.
  • Inflammatory dermatoses: reduces redness, swelling and itching associated with eczema or contact dermatitis.
  • Post‑menopausal skin aging: improves skin elasticity and hydration through estrogenic effects.

How It Works

  • Estradiol hemihydrate binds to estrogen receptors (ERα and ERβ) acting as an agonist, thereby promoting gene transcription that supports tissue integrity and moisture. Prednisolone sesquihydrate engages glucocorticoid receptors, inhibiting phospholipase A2 and downstream prostaglandin and cytokine production, resulting in anti‑inflammatory and immunosuppressive effects at the site of application.

Side Effects

Common Side Effects

  • Local skin irritation or burning sensation.
  • Mild itching or pruritus.
  • Dryness or peeling of the applied area.
  • Transient erythema.
  • Hyperpigmentation at the site.
  • Folliculitis or mild acneiform eruption.

Serious or Rare Side Effects

  • Allergic contact dermatitis with swelling and vesiculation.
  • Severe skin atrophy or thinning.
  • Systemic estrogenic effects such as thromboembolic events.
  • Adrenal suppression with prolonged use.
  • Cushingoid appearance or systemic corticosteroid toxicity.
  • Secondary bacterial or fungal infection of the treated skin.

Precautions & Warnings

Before using Linoladiol-H N, consider the following precautions:

  • Pregnancy: avoid use unless the prescriber determines benefits outweigh potential risks.
  • Breastfeeding: not recommended due to possible transfer of active ingredients.
  • Known hypersensitivity: discontinue immediately if allergic reaction occurs.
  • Infected or broken skin: do not apply on areas with active infection or open wounds.
  • Hormone‑sensitive conditions: use with caution in patients with a history of estrogen‑dependent tumors.
  • Store at ambient temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Linoladiol-H N may interact with other medicines as follows:

Major Interactions (Avoid)

  • Oral systemic estrogen therapy: increased risk of thromboembolic events.
  • Systemic corticosteroids: additive immunosuppression and adrenal suppression.
  • Antifungal azoles (e.g., ketoconazole): may raise local corticosteroid concentrations.

Moderate Interactions (Monitor Closely)

  • CYP450 enzyme inducers (e.g., rifampicin): may reduce corticosteroid efficacy.
  • Hormonal contraceptives: possible reduction in contraceptive effectiveness.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs) applied nearby: may increase local skin irritation.

Frequently Asked Questions

Linoladiol-H N is a topical combination of estradiol hemihydrate and prednisolone sesquihydrate designed to address estrogen deficiency‑related skin changes and to provide local anti‑inflammatory relief for conditions such as eczema, dermatitis, and post‑menopausal skin aging.

Estradiol hemihydrate acts as an estrogen receptor agonist. By binding to ERα and ERβ in skin cells, it stimulates gene expression that promotes tissue hydration, collagen synthesis, and maintenance of the epithelial barrier, helping to reverse estrogen‑related skin atrophy.

The appropriate dose of Linoladiol-H N is determined by the prescribing healthcare professional based on the patient’s condition, age, and response. The prescriber will specify the amount to apply, frequency, and duration of therapy.

Safety in pregnancy and lactation has not been established. The product should be avoided unless the prescriber judges that the potential benefit justifies any possible risk to the fetus or infant.

To place an order, submit an enquiry on the Linoladiol-H N 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 (including any cold‑chain requirements) and necessary import documentation.

Unlike single‑ingredient estrogen creams, Linoladiol-H N combines estrogen with a corticosteroid, offering both hormonal restoration and anti‑inflammatory action in one formulation. This dual mechanism can be advantageous for patients who need estrogenic skin benefits while also requiring control of inflammation.

Store the product at ambient temperature, preferably below 25 °C, in its original packaging. Keep it away from direct sunlight, moisture, and heat sources to maintain stability and potency.

Linoladiol-H N is applied topically to the affected skin area. The prescriber will advise the amount to use per application, the frequency (e.g., once or twice daily), and the total duration of treatment.

Serious risks include severe allergic reactions, systemic estrogenic effects such as thromboembolic events, adrenal suppression from the corticosteroid component, and secondary skin infections. Patients should report any signs of swelling, severe rash, unexplained bruising, or infection promptly.

Linoladiol-H N should not be used by individuals with known hypersensitivity to estradiol, prednisolone, or any excipients, by patients with active skin infections at the application site, and by those with a history of estrogen‑dependent tumors unless specifically directed by a specialist.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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