They deliver from Korea Worldwide, i live in Germany, they Sometimes faster then Deliveries from Germany, i dont know how they do it. They deliver high quality at best price. You dont get all of that anywhere else.
Nikola Kolobarić
XEOMIN 100U
XEOMIN 100U is a prescription botulinum toxin type A product developed by Merz, containing 100 Units of purified 150 kDa botulinum neurotoxin type A…
XEOMIN 100U is a prescription botulinum toxin type A product developed by Merz, containing 100 Units of purified 150 kDa botulinum neurotoxin type A per vial. Formulated without accessory complexing proteins, XEOMIN offers a distinctive approach to professional aesthetic treatment of dynamic facial lines.
The Korean-market presentation is approved for the temporary improvement of moderate-to-severe upper facial lines, including glabellar lines, lateral canthal lines (crow's feet) and horizontal forehead lines in specified adult age groups.
Supplied as a lyophilized powder for solution for injection, XEOMIN 100U combines a purified neurotoxin formulation with convenient unopened storage conditions of 1–25°C and a published 36-month shelf life.
Key Features
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100 Units of botulinum toxin type A per vial
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Purified 150 kDa neurotoxin
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Formulated without accessory complexing proteins
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Contains incobotulinumtoxinA
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Developed by Merz, a German pharmaceutical company
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Approved in South Korea for temporary improvement of specified upper facial lines
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Lyophilized powder for solution for injection
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Unopened storage at 1–25°C
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Published shelf life of 36 months
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Single-vial presentation for professional medical use
Applications & Indications
The Korean-market XEOMIN 100U presentation is approved for the temporary improvement of moderate-to-severe upper facial lines associated with facial muscle activity.
Glabellar Lines (Frown Lines)
Temporary improvement of moderate-to-severe glabellar lines associated with corrugator and/or procerus muscle activity in adults aged 18–65 years.
Lateral Canthal Lines (Crow's Feet)
Temporary improvement of moderate-to-severe lateral canthal lines associated with orbicularis oculi muscle activity in adults aged 18–60 years.
Horizontal Forehead Lines
Temporary improvement of moderate-to-severe horizontal forehead lines associated with frontalis muscle activity in adults aged 18–65 years.
These indications and age ranges reflect the published South Korean product information.
Composition
Each XEOMIN 100U vial contains:
Active Ingredient
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IncobotulinumtoxinA (Clostridium botulinum neurotoxin type A): 100 Units
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Neurotoxin molecular weight: 150 kDa
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Accessory complexing proteins: None
Excipients
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Human Serum Albumin
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Sucrose
The product is supplied as a lyophilized powder for solution for injection.
Product Specifications
Product Name: XEOMIN 100U
Product Category: Botulinum Toxin Type A
Active Ingredient: IncobotulinumtoxinA
Strength: 100 LD50 Units per Vial
Neurotoxin Molecular Weight: 150 kDa
Complexing Proteins: None
Formulation: Lyophilized Powder for Solution for Injection
Presentation: Single Vial
Quantity: 1 Vial per Box
Brand: XEOMIN by Merz
Manufacturer: Merz Pharma GmbH & Co. KGaA
Brand Origin: Germany
Market Presentation: South Korea
Unopened Storage: 1–25°C
Shelf Life: 36 Months from Manufacture
Purified 150 kDa Neurotoxin Formulation
XEOMIN contains purified botulinum neurotoxin type A without the accessory complexing proteins found in certain other botulinum toxin formulations.
The active 150 kDa neurotoxin is responsible for XEOMIN's pharmacological activity. Its formulation without complexing proteins is a defining characteristic of the product.
XEOMIN's potency Units are specific to its biological assay and are not interchangeable with the Units of other botulinum toxin products.
How XEOMIN Works
XEOMIN temporarily inhibits the release of acetylcholine at peripheral cholinergic nerve endings, reducing activity in the targeted muscles.
In aesthetic medicine, this mechanism temporarily reduces the muscle contractions responsible for dynamic facial lines, improving the appearance of approved upper facial wrinkles.
The effects are temporary, with clinical outcomes varying according to the individual and the approved treatment indication.
What's in the Box
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1 × XEOMIN 100U vial containing lyophilized botulinum toxin type A
Storage & Handling
Unopened Korean-market XEOMIN 100U should be stored in a sealed container at 1–25°C.
Shelf Life: 36 months from the date of manufacture.
Refrigeration is not required for unopened vials when stored within the approved temperature range.
Following reconstitution, the prepared solution may be refrigerated at 2–8°C for up to 24 hours. As XEOMIN contains no antimicrobial preservative, Merz Korea recommends using the prepared solution promptly.
Storage, handling and administration must follow the current approved Korean product information and applicable professional requirements.
Professional Use Only
This product is intended for qualified medical or aesthetic professionals and is not intended for self-administration.
Before Use
Always review the product packaging, labeling, and manufacturer information before use. Do not use if the product in the package is damaged or if product integrity is in question; contact us.
Regulatory Notice
Product requirements and permitted uses may vary by country. Buyers are responsible for ensuring compliance with applicable local regulations.
Disclaimer: Product information provided on this website is for general informational purposes only and does not constitute medical advice, treatment guidance, or instructions for use.
Intended Use
This product should be used only for its intended purpose and in accordance with the manufacturer’s product information.
Before Use
Always review the product packaging, labeling, and manufacturer information before use. Do not use if the product in the package is damaged or if product integrity is in question; contact us.
Regulatory Notice
Product requirements and permitted uses may vary by country. Buyers are responsible for ensuring compliance with applicable local regulations.
Disclaimer: Product information provided on this website is for general informational purposes only and does not constitute medical advice, treatment guidance, or instructions for use.
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Brunodermafiller is committed to offering you the most competitive prices. Depending on the products and quantities you purchase, you can save up to 20% compared to other distributors.
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How long does the shipping take?
- USA, Canada, Japan: 2–5 business days
- Europe (excluding Germany and Italy): 3–5 business days
- Germany & Italy: 3–6 business days (tracking available after about 5 working days)
- South Africa: 7+ business days
- Dominican Republic: 8–12 business days
Average worldwide delivery time is 3–5 business days. Delays may occur due to customs clearance or flight schedules.
How is my order packaged?
For aesthetic treatment products such as injectables, we use temperature-controlled packaging when required, following strict safety and hygiene standards. All parcels are shipped in discreet packaging by default. No product names or medical terms appear on the outside of the box.
How to modify or cancel my order?
To modify or cancel your order, please contact us as soon as possible at info@brunodermalfiller.com.If your order hasn’t been processed or shipped yet, we’ll do our best to accommodate your request. Once it’s been dispatched, changes or cancellations are no longer possible, but you may be eligible for a return or exchange after delivery
The product packaging looks different. Is it authentic?
Yes, in many cases this is completely normal. Manufacturers may update their packaging, labels, security features, or product design without changing the product itself.
Packaging, logos, colours, security seals, QR codes, and labels may vary between production batches. If you have any concerns, please contact our support team with your order number and clear photos of the product and packaging.
Which saline or lidocaine should I use with this product?
Please follow the manufacturer's instructions for the specific product you have purchased. Preparation requirements vary between products and manufacturers.
Always refer to the manufacturer's official instructions supplied with the product. Products should only be prepared and administered by appropriately qualified healthcare professionals in accordance with applicable local regulations.
