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Advanced technology targets and eliminates unwanted hair, leaving your skin feeling silky and rejuvenated.
IPL Skin Rejuvenation
IPL uses the power of intense pulse light to minimize the appearance of age spots, sun spots, broken vessels, and more.
Sublative RF
A revolutionary treatment that utilizes RF technology and heat to enhance your complexion, smooth skin texture, and promote collagen renewal
Vivace Ultra Microneedling RF
This best in class device combines microneedling with radiofrequency energy and a specialized treatment serum and a cooling peptide mask to provide patients with superior, natural-looking results.
Plasma Pen Fibroblast
A non-invasive treatment harnessing plasma technology to tighten and rejuvenate, leaving you with a smoother, youthful appearance.
Red Light Therapy
Relax in a quiet, private room while the red light heals and reduces the signs of aging.
lasers + lights
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Email
info@lakeshoreskinandbody.com
Phone
906-273-0512
Location
153 W. Washington Street, LL
Marquette, MI 49855
longevity
6-9 months
recovery
no downtime
WHAT IT TREATS
FROWN LINES, FOREHEAD WRINKLES, CROWSFEET, GUMMY SMILE
We are thrilled to have been selected by Revance Aesthetics to be one of the first practices in the world, and the only practice in the region to offer Daxxify, the world’s first peptide-powered neurotoxin that has been proven effective for twice as long as other wrinkle relaxers on the market.
IMPORTANT SAFETY INFORMATION
for DAXXIFYTM (daxibotulinumtoxinA-Ianm) injection DAXXIFYTM may cause serious side effects that can be life threatening. Get medical help right away if you have any of these problems any time (hours to weeks) after injection of DAXXIFYTM: • Problems swallowing, speaking, or breathing due to weakening of associated muscles can be severe and result in loss of life. You are at the highest risk if these problems are pre-existing before injection. Swallowing problems may last for several months. • Spread of toxin effects. The effect of botulinum toxin may affect areas away from the injection site and cause serious symptoms that include loss of strength and all-over muscle weakness, double vision, blurred vision and drooping eyelids, hoarseness or change or loss of voice, trouble saying words clearly, loss of bladder control, trouble breathing, and trouble swallowing. Do not receive DAXXIFYTM if you are allergic to any of the ingredients in DAXXIFYTM (see Medication Guide for ingredients); had an allergic reaction to any other botulinum toxin product such as rimabotulinumtoxinB (MYOBLOC®), onabotulinumtoxinA (BOTOX®/BOTOX® Cosmetic), abobotulinumtoxinA (DYSPORT®), incobotulinumtoxinA (XEOMIN®) or prabotulinumtoxinA-xvfs (JEUVEAU®); or have a skin infection at the planned injection site. DAXXIFYTM dosing units are not the same as, or comparable to, any other botulinum toxin product. Tell your healthcare provider about all your medical conditions, including any side effects from botulinum toxin products, including dry eye; breathing, swallowing, bleeding, or heart problems; plans to have surgery; weakness of forehead muscles; drooping eyelids; have had surgery on your face; are pregnant or breastfeeding or plan to become pregnant or breastfeed. Tell your healthcare provider about all the medicines you take, including prescription and over-the- counter medicines, vitamins, and herbal supplements. Using DAXXIFYTM with certain other medicines may cause serious side effects. Do not start any new medicines until you have told your healthcare provider that you have received DAXXIFYTM in the past. Especially tell your healthcare provider if you have received any other botulinum toxin product in the last 4 months or any in the past, and exactly which product you received (such as BOTOX®, BOTOX® Cosmetic, MYOBLOC®, DYSPORT®, XEOMIN®, or JEUVEAU®). DAXXIFYTM may cause serious side effects, including allergic reactions (such as itching, rash, redness, swelling, wheezing, trouble breathing, or dizziness or feeling faint), heart problems (such as irregular heartbeat and heart attack), and eye problems (including dry eye, reduced blinking, and corneal problems). Tell your healthcare provider or get medical help right away if you experience a serious side effect. No serious adverse events of distant spread of toxin effect associated with dermatologic use of DAXXIFYTM have been reported in clinical studies at the dose of 40 Units for glabellar lines. The most common side effects of DAXXIFYTM include headache, eyelid drooping, and loss of ability to move the muscles in your face. These are not all the possible side effects of DAXXIFYTM. For more information, see the full Prescribing Information including Boxed Warning, and refer to the Medication Guide or talk with your doctor. To report side effects associated with DAXXIFYTM, please call 1-877-373-8669. You may also report side effects to the FDA at 1-800-FDA-1088 or visit www.fda.gov/medwatch. APPROVED USE DAXXIFYTM is a prescription medicine that is injected into muscles and used in adults to temporarily improve the look of moderate to severe frown lines between the eyebrows. DAXI-001723
Why are peptides important?
All frown line treatments require a special ingredient to stabilize botulinum toxin A, the protein responsible for helping smooth moderate to severe frown lines. For instance, BOTOX® Cosmetic uses human serum albumin (HSA), a blood product, as its stabilizer. Dysport®, another frown line treatment, uses HSA as a stabilizer and cow’s milk protein as a protectant.
DAXXIFY is unique because it is the only formulation that uses a novel peptide as a stabilizer and does not contain human or animal byproducts.
Is DAXXIFY well studied?
DAXXIFY was studied in the largest-ever clinical study conducted for a frown line treatment and included more than 2,400 people across different ages and skin types. There were no serious treatment-related side effects in clinical trials for DAXXIFY.
The active ingredient in DAXXIFY is botulinum toxin type A, an ingredient that has been used in frown line treatments for more than 20 years
96% of people treated with DAXXIFY were satisfied with their results†
†96% of patients reported they were satisfied on a 7-point scale when evaluated at 4 weeks in clinical studies.
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