Elotox® is a high-purity Botulinum Toxin Type A developed using advanced Quality by Design (QbD) principles to deliver consistent clinical outcomes, predictable diffusion, and reproducible potency. Designed exclusively for licensed medical professionals, Elotox meets the demands of modern aesthetic and therapeutic practice while offering a reliable, premium alternative to market-leading brands.  

Elotox® is a high-purity Botulinum Toxin Type A developed using advanced Quality by Design (QbD) principles to deliver consistent clinical outcomes, predictable diffusion, and reproducible potency. Designed exclusively for licensed medical professionals, Elotox meets the demands of modern aesthetic and therapeutic practice while offering a reliable, premium alternative to market-leading brands.  

Elotox® is a high-purity Botulinum Toxin Type A developed using advanced Quality by Design (QbD) principles to deliver consistent clinical outcomes, predictable diffusion, and reproducible potency. Designed exclusively for licensed medical professionals, Elotox meets the demands of modern aesthetic and therapeutic practice while offering a reliable, premium alternative to market-leading brands.


100% Reproducibility through QbD-Based Quality Control
100% Purity through a Patented Filtration System

Elotox is manufactured under a fully standardized and validated production system to ensure uniform performance across every vial and every batch.

  • Advanced, standardized production process

  • Consistent unit potency and biological activity

  • Full batch-to-batch traceability

  • Comprehensive safety and quality control at every stage

This QbD-driven approach ensures predictable clinical results and long-term practitioner confidence.

Elotox achieves exceptional purity through a proprietary short-term purification process designed to eliminate unnecessary proteins while preserving biological activity.

  • Unique short-term purification process (1 day / 1 week)

  • Removal of non-essential proteins for enhanced stability

  • Clean formulation designed for predictable diffusion and effect

Purity Result:
99.6% purity confirmed by SEC-HPLC, indicating near-complete removal of unwanted proteins and contaminants.

Reconstitution Instructions
  • Using a sterile syringe, draw 2.5 mL of non-preserved 0.9% Sodium Chloride (recommended diluent).

  • Insert the needle into the Elotox vial (vacuum-sealed) and slowly inject the saline.

  • Inject gently to avoid foaming or bubble formation.

  • Gently swirl until the lyophilized powder is fully dissolved and the solution is clear and particle-free.

  • Record the date and time of reconstitution.

  • Use the reconstituted solution within 24 hours.

  • Store the reconstituted product at 2–8°C until use.

Onset, Duration & Treatment Interval
  • Initial improvement: within 1 week

  • Maximum effect: 5–6 weeks

  • Duration of results: up to 4 months

  • Minimum interval between treatments: 3 months


Safety Information

Seek immediate medical attention if you experience any of the following issue: at any time (from hours to weeks) after receiving a treatment:

- Difficulty swallowing, speaking, or breathing: Weakness in the associated muscles can be severe and life-threatening, especially if you had pre-existing conditions. Swallowing difficulties may persist for several months.

Potentional side effects
Allergic reactions

In rare cases, loss of strength, general muscle weakness, vision disturbances, or dizziness may occur within hours to weeks following treatment. If such symptoms develop, patients should refrain from driving, operating heavy machinery, or engaging in other potentially hazardous activities until symptoms resolve.

Other potential side effects include dry mouth, discomfort or pain at the treatment site, fatigue, headaches, neck pain, and various eye-related issues such as double vision, blurred vision, decreased eyesight, drooping eyelids or eyebrows, eyelid swelling, and dry eyes.

 

Serious allergic reactions have been reported, including itching, rashes, red welts, wheezing, asthma symptoms, or dizziness. Seek immediate medical help if you experience wheezing, asthma symptoms, or feel faint.

Do Not Use If You

Are allergic to any ingredients in Elotox (refer to the Medication Guide for details). Have had an allergic reaction to any botulinum toxin product, such as Myobloc (rimabotulinumtoxinB), Dysport (abobofulinumtoxinA), or Xeomin (incobotulinumtoxinA). Have a skin infection at the intended application site.

Post-Treatment Care Instrustions and Safety Considerations

Avoid touching or massaging the treated area for at least 24 hours, staying upright for 4-6 hours, and avoiding strenuous exercise for 24 hours

Important Safety Warnings and Contraindications

Inform your doctor about any muscle or nerve conditions, such as ALS, myasthenia gravis, or Lambert-Eaton syndrome, as these may

increase the risk of serious side effects like difficulty swallowing or breathing.

Inform your doctor about all medical conditions, including plans for surgery, past facial surgeries, issues raising your eyebrows, drooping eyelids, unusual facial changes, and if you are pregnant or breastfeeding (it is unknown if Elotox can harm your unborn baby or ifit passes into breast milk).

Inform your doctor about all medications you are toking, including prescriptions, over-the counter drugs, vitamins, and herbal supplements Combining Elotox with certain medications may lead to serious side effects. Do not start any new medications without informing your doctor about your recent Elotox treatment.

Notify your doctor if you have: Received any other botulinum foxin product in the last four months. Recently had injections of botulinum toxin products like Myobloc, Dysport, or Xeomin (please specify which product). Recently received an antibiotic application or are taking muscle relaxants, allergy or cold medications, sleep aids, or blood thinners.