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EJAL

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Ejal40 is positioned as a next-generation skin rejuvenation therapy aimed at combatting signs of aging, dehydration, and photodamage. By revitalizing the ECM, EJAL40 stimulates the creation of new collagen and elastin fibers, ultimately improving skin compactness, smoothness, and structure.

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EJAL40 Bio-Revitalizing Gel

$49.00

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What is EJAL40?

EJAL40 is a bio-revitalizing gel formulated with medium molecular weight hyaluronic acid (HA), designed to restructure and restore the extracellular matrix (ECM) of the skin. It supports fibroblast regeneration and enhances cellular activities critical for skin health, such as the synthesis of collagen, elastin, and endogenous hyaluronic acid. With a concentration of 40 mg of HA per 2 ml syringe, EJAL40 is presented as a sterile, biodegradable, isotonic pre-filled syringe intended for intradermal application. Its innovative formulation contains different molecular weights of HA—10 mg (1200 KDa), 20 mg, and 40 mg (1200–1800 KDa)—to enhance elasticity, hydration, and skin longevity.

Check out our article detailing Ejal40 Before and After results.

How Long Does EJAL40 Last?

The duration of EJAL40's effects depends on the treatment protocol and the individual’s skin condition. Typically, the protocol involves:

  • 3 treatment sessions spaced one month apart.

  • A maintenance session every two months depending on the aging level.

  • Repeat cycle twice per year for sustained benefits.

The long-lasting improvements in skin quality result from the stimulation of fibroblasts and the enhanced biosynthesis of structural skin components, making EJAL40 not only a temporary filler but a regenerative solution.

What Are the Indications of EJAL40?

EJAL40 is particularly indicated for:

  • Skin laxity and reduced elasticity

  • Fine lines and wrinkles

  • Dehydrated or sun-damaged skin

  • Stretch marks

  • Pre-treatment before the use of dermal fillers

Its primary function is to regenerate the skin’s extracellular matrix and counteract the natural decline of hyaluronic acid associated with aging. By restoring hydration and structural integrity, it also serves as a preventive measure against photoaging and is suitable for patients preparing for more invasive aesthetic procedures.

What Contraindications or Side Effects Does EJAL40 Entail?

While EJAL40 is well-tolerated in most patients, certain contraindications and precautions must be observed:

Contraindications:

  • History of hypertrophic scars

  • Autoimmune diseases or ongoing immunotherapy

  • Known hypersensitivity to hyaluronic acid or formulation components

  • Pregnancy or breastfeeding

  • Patients under 18 years of age

Cautions:

  • Use only under physician supervision in patients on anticoagulant or anti-inflammatory medications

  • Do not inject in areas with active inflammation or infection (e.g., acne, herpes)

Side Effects:

  • As with most HA-based injectables, possible side effects include:

    • Mild swelling

    • Redness

    • Bruising at the injection site

    • Temporary discomfort These effects are typically short-lived and resolve within a few days post-treatment.

How Do You Store EJAL40?

EJAL40 must be stored in appropriate conditions to maintain product integrity:

  • Room temperature (follow exact manufacturer storage guidance)

  • Avoid exposure to direct sunlight

  • Do not freeze

  • Ensure the syringe remains in sterile packaging until use

Storage stability and sterility are critical for the safety and efficacy of this medical device, and all product use should be guided by trained professionals.

Who Manufactures EJAL40?

EJAL40 is manufactured in Italy, and the product is marketed as a CE 1984 certified medical device, indicating compliance with European safety and quality standards. It is certified under:

  • UNI EN ISO 13485 (medical devices)

  • GMP - UNI EN ISO 22716 (good manufacturing practices for cosmetics)

The product is distributed by LPG Clinics Wholesale, which operates internationally. EJAL40 is currently available in 62 countries and has seen over 200,000 treatments performed since its market entry in 2015.

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