You are currently viewing Keep exploring what works for you and brings you joy.

Keep exploring what works for you and brings you joy.

GP Joy – September

Xeomin is a uniquely purified antiwrinkle injection (free of unnecessary proteins) that temporarily treats frown lines. Call us to learn more today!

#DareToSelfCare #LaterFrownLines #HelloXeomin
For full Prescribing Information including Boxed Warning and Medication Guide, see xeominaesthetic.com.

Intended for US audiences only. Xeomin® is an FDA-approved treatment used to temporarily improve the look of moderate to severe frown lines between the eyebrows (glabellar lines) in adults. Ask your doctor to tell you all about Xeomin. The effects of Xeomin may
spread hours to weeks after injection causing serious symptoms. Alert your doctor right away as difficulty swallowing, speaking, breathing, eye problems or muscle weakness can be a sign of a life-threatening condition. Side effects may include allergic reactions or injection-site pain, eyelid drooping, and swelling.

Xeomin is available by prescription only.

Xeomin Questions Answered – September

We consider ourselves quite the Xeomin Xperts. The best treatments begin with research. Contact us to learn more about Xeomin, a
uniquely purified antiwrinkle injection (free of unnecessary proteins) for frown lines today!

#DareToSelfCare #LaterFrownLines #HelloXeomin

For full Prescribing Information including Boxed Warning and Medication Guide, see xeominaesthetic.com.
Intended for US audiences only. Xeomin® is an FDA-approved treatment used to temporarily improve the look of moderate to severe frown lines between the eyebrows (glabellar lines) in adults. Ask your doctor to tell you all about Xeomin. The effects of Xeomin may
spread hours to weeks after injection causing serious symptoms. Alert your doctor right away as difficulty swallowing, speaking, breathing, eye problems or muscle weakness can be a sign of a life-threatening condition. Side effects may include allergic reactions or injection-site pain, eyelid drooping, and swelling.

Xeomin is available by prescription only.

National Coffee Day – 9/29

Coffee is the perfect excuse to catch a break. While you’re at it, give us a call and we can chat about Xeomin, a uniquely purified antiwrinkle injection (free of unnecessary proteins) that’s proven to temporarily relax your frown lines.

#DareToSelfCare #LaterFrownLines # HelloXeomin

For full Prescribing Information including Boxed Warning and Medication Guide, see xeominaesthetic.com. Intended for US audiences only. Xeomin® is an FDA-approved treatment used to temporarily improve the look of moderate to severe frown lines between the eyebrows (glabellar lines) in adults. Ask your doctor to tell you all about Xeomin. The effects of Xeomin may spread hours to weeks after
injection causing serious symptoms. Alert your doctor right away as difficulty swallowing, speaking, breathing, eye problems or muscle
weakness can be a sign of a life-threatening condition. Side effects may include allergic reactions or injection-site pain, eyelid drooping, and swelling.

Xeomin is available by prescription only.

$50 Off

Want to save money + earn points while getting the beauty treatments you love? We’re now offering the Xperience+ Loyalty Program
with the most loyalty rewards for Xeomin, Radiesse, and Belotero treatments*! Ask us about the program and how you can start
saving today!

*Products not studied in combination use.

For full Prescribing Information including Boxed Warning and Medication Guide, see xeominaesthetic.com.

Intended for US audiences only. Xeomin® is an FDA-approved treatment used to temporarily improve the look of moderate to
severe frown lines between the eyebrows (glabellar lines) in adults. Ask your doctor to tell you all about Xeomin. The effects
of Xeomin may spread hours to weeks after injection causing serious symptoms. Alert your doctor right away as difficulty swallowing,
speaking, breathing, eye problems or muscle weakness can be a sign of a life-threatening condition. Side effects may include allergic
reactions or injection-site pain, eyelid drooping, and swelling.

Xeomin is available by prescription only.

Indications and Usage

XEOMIN® (incobotulinumtoxinA) for injection, for intramuscular use is indicated for the temporary improvement in the appearance of moderate to severe glabellar lines with corrugator and/or procerus muscle activity in adult patients.

Important Safety Information

WARNING: DISTANT SPREAD OF TOXIN EFFECT
See full prescribing information for complete BOXED WARNING.

The effects of XEOMIN and all botulinum toxin products may spread from the area of injection to produce symptoms consistent with botulinum toxin effects. These symptoms have been reported hours to weeks after injection. Swallowing and breathing difficulties can be life threatening and there have been reports of death. The risk of symptoms is probably greatest in children treated for spasticity but symptoms can also occur in adults, particularly in those patients who have underlying conditions that would predispose them to these symptoms.

CONTRAINDICATIONS

Hypersensitivity reactions have been reported with botulinum toxin products (anaphylaxis, serum sickness, urticaria, soft tissue edema, and dyspnea). If serious and/or immediate hypersensitivity reactions occur further injection of XEOMIN should be discontinued and appropriate medical therapy immediately instituted. XEOMIN is contraindicated in patients with known hypersensitivity to any botulinum toxin preparation or to any of the components in the formulation.

Use in patients with an infection at the injection site could lead to severe local or disseminated infection.
XEOMIN is contraindicated in the presence of infection at the proposed injection site(s).

WARNINGS AND PRECAUTIONS

  • The potency units of XEOMIN are specific to the preparation and assay method used and are not interchangeable with other preparations of botulinum toxin products. Therefore, Units of biological activity of XEOMIN cannot be compared to or converted into Units of any other botulinum toxin products.
  • Treatment with XEOMIN and other botulinum toxin products can result in swallowing or breathing difficulties. Patients with pre-existing swallowing or breathing difficulties may be more susceptible to these complications. When distant effects occur, additional respiratory muscles may be involved. Patients may require immediate medical attention should they develop problems with swallowing, speech, or respiratory disorders. Dysphagia may persist for several months, which may require use of a feeding tube. Aspiration may result from severe dysphagia [See BOXED WARNING].
  • Individuals with peripheral motor neuropathic diseases, amyotrophic lateral sclerosis, or neuromuscular junctional disorders (e.g., myasthenia gravis or Lambert-Eaton syndrome) should be monitored particularly closely when given botulinum toxin. Patients with neuromuscular disorders may be at increased risk of clinically significant effects including severe dysphagia and respiratory compromise from typical doses of XEOMIN.
  • Glabellar Lines: Do not exceed the recommended dosage and frequency of administration of XEOMIN. In order to reduce the complication of ptosis the following steps should be taken:
    • avoid injection near the levator palpebrae superioris, particularly in patients with larger brow depressor complexes;
    • corrugator injections should be placed at least 1 cm above the bony supraorbital ridge.
  • XEOMIN contains human serum albumin. Based on effective donor screening and product manufacturing processes, it carries an extremely remote risk for transmission of viral diseases and variant Creutzfeldt-Jakob disease (vCJD). There is a theoretical risk for transmission of CreutzfeldtJakob disease (CJD), but if that risk actually exists, the risk of transmission would also be considered extremely remote. No cases of transmission of viral diseases, CJD or vCJD have ever been reported for albumin.

ADVERSE REACTIONS

Glabellar Lines: The most commonly observed adverse reaction (incidence ≥ 2% of patients and greater
than placebo) for XEOMIN was Headache (5.4%). DRUG INTERACTIONS Co-administration of XEOMIN
and aminoglycoside or other agents interfering with neuromuscular transmission, (e.g., muscle relaxants),
should only be performed with caution as these agents may potentiate the effect of the toxin.
Use of anticholinergic drugs after administration of XEOMIN may potentiate systemic anticholinergic effects.
The effect of administering different botulinum toxin products at the same time or within several months of
each other is unknown. Excessive neuromuscular weakness may be exacerbated by administration of
another botulinum toxin prior to the resolution of the effects of a previously administered botulinum toxin.

USE IN PREGNANCY

There are no adequate data on the developmental risk associated with the use of XEOMIN in pregnant
women. XEOMIN should be used during pregnancy only if the potential benefit justifies the potential risk to
the fetus.

PEDIATRIC USE

Safety and effectiveness of XEOMIN in patients less than 18 years of age have not been established.
US-XEA-2100169
Copyright © 2021 Merz North America, Inc. All rights reserved. Merz Aesthetics and Xeomin are registered
trademarks of Merz Pharma GmbH & Co. KGaA.
To learn more about other Merz North America brands, please visit www.merzusa.com.

Leave a Reply