Only for Licensed Professionals
Only for Licensed Professionals

In the realm of cosmetic enhancements, precision and performance are paramount. XEOMIN® (incobotulinumtoxinA) stands out in the crowd, offering a meticulously crafted solution through its Smart Toxin Formula. What sets XEOMIN® apart is not just its effectiveness in smoothing frown lines, but also its commitment to purity and safety.
At the core of XEOMIN® lies a proprietary process known as XTRACT Technology™. This innovative technique involves a meticulous double filtration process, ensuring that the final product is free from unnecessary proteins. By stripping away these extraneous elements, XEOMIN® focuses solely on delivering the active ingredient, optimized for efficacy and safety.
XEOMIN®’s unique formulation isn't just about immediate results; it's about the journey of continued improvement. With each treatment session, patients can expect consistent outcomes, thanks to the purity and potency of XEOMIN®’s Smart Toxin Formula. Receiving XEOMIN® regularly helps maintain results over time.
Read our comprehensive article, which answers the question: "Does XEOMIN® or Botox Last Longer?"
XEOMIN® (incobotulinumtoxinA) is a prescription medication injected into muscles and used to temporarily improve the appearance of moderate to severe frown lines between the eyebrows (glabellar lines) in adults. XEOMIN® contains botulinum toxin type A, a purified botulinum toxin protein derived from Clostridium botulinum. If you're considering taking XEOMIN®, consult a licensed medical professional to determine its suitability.
XEOMIN® has undergone rigorous clinical trials to demonstrate its effectiveness in treating glabellar lines. These trials, involving 547 healthy adult patients, utilized a randomized, double-blind, multicenter, placebo-controlled design to ensure robust and reliable results.
In these studies, patients received 20 units of XEOMIN® and were evaluated based on a predefined assessment scale by both medical professionals and patients themselves. Treatment success was defined as a 2-grade improvement on a 4-point scale.
The results showed that XEOMIN® outperformed the placebo, with a significantly higher percentage of patients achieving treatment success on Day 30 in both trials. Specifically, success rates were reported at 60% and 48% for XEOMIN®, compared to 0% for the placebo in both studies. These findings provided compelling evidence of XEOMIN®'s efficacy in reducing glabellar lines, leading to XEOMIN® FDA approval for this indication in 2011.
When recommending XEOMIN® to patients for the treatment of frown lines between the eyebrows, it's essential to be vigilant about potential side effects and ensure patients are well-informed. While XEOMIN® is generally safe and effective when administered correctly, it can lead to serious adverse reactions in some individuals.
XEOMIN® has the potential to cause allergic reactions, which may manifest as itching, rash, redness, swelling, wheezing, asthma symptoms, or feelings of dizziness or faintness. If a patient experiences any of these symptoms after receiving XEOMIN®, prompt medical care should be sought. It's crucial to emphasize the importance of notifying their doctor immediately in such instances.
In clinical trials focusing on the treatment of frown lines, headache emerged as the most common side effect associated with XEOMIN®. Additionally, patients may experience other side effects, such as muscle weakness, blurred vision, or drooping eyelids, within hours to weeks of treatment initiation. Instruct patients to refrain from engaging in activities requiring concentration or coordination, such as driving or operating equipment, if they experience these symptoms.
The injection site plays a crucial role in ensuring optimal results and minimizing problems such as localized pain, bruising, or swelling. Indications and contraindications must be carefully assessed before administering XEOMIN® injections, especially in individuals with pre-existing muscle or nerve problems. Additionally, problems such as swallowing, breathing, or excessive weakness may occur in rare cases. It is essential to consult a licensed medical provider before taking XEOMIN®.
Encourage prospective patients to engage in an open dialogue with their doctor, so they can address any concerns, discuss medical history, and gain a comprehensive understanding of what to expect from XEOMIN® treatment. Providing patients access to information, such as the XEOMIN® website, FDA-approved product labeling, and dedicated helplines, enables them to make informed choices about their aesthetic journey.
For licensed medical professionals and clinics, it’s vital to buy XEOMIN® from reputable sources only to ensure authenticity and adherence to proper application standards. Many dermal fillers clinics prefer to buy XEOMIN® online to streamline their supply chain. Whether you need XEOMIN 100u for aesthetic applications or botulinum toxin products for therapeutic uses, make sure to check for trusted suppliers. Contact our team for information on how to buy XEOMIN® wholesale, ensuring quality and authenticity for your clinic’s needs.
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