DMK Skin Revision

DMK Skin Revision

Rejuvenate & Refresh

You exercise and give your body solid nutrition to help it feel its best. Why wouldn’t you treat your skin the same way, to have it looking and feeling its best? Treat acne scarring, fine lines and wrinkles, redness, skin pigmentation and other issues with DMK Skin Revision. The program is backed by science — biochemistry to be exact — and keeps the unique needs and wants of your skin in mind when matching you with a treatment plan that will leave your skin looking younger, healthier, and refreshed.

DMK Skin Revision is a customized treatment series. A cornerstone is enzyme therapy, a treatment plan based on a series of four principles: remove, rebuild, protect and maintain. Remove dead skin cells and detox the surface of your skin. Rebuild your skin’s natural processes using exfoliating techniques. Protect your skin with consistent care provided to you as part of your treatment plan. Maintain an optimal balance of collagen production and the resulting rejuvenating effects with continued revision treatments. 

If you’re seeking that ideal recipe for rejuvenated skin, get on board with DMK Skin Revision in Orange County. Our experts at the Med Lounge can help develop a customized plan for you that will take years off your skin.

Benefits of DMK Skin Revision

Restore skin

Improve tone and texture

Feel young again

Individualized skincare

Reverse effects of aging

Detox your skin

Exfoliate and rejuvenate

Bring skin back to balance

Education on skincare

Safe and effective

Frequently Asked Questions

DMK Skin Revision is a treatment program based on your personal biochemistry that matches you with products and a range of treatments that result in healthier, younger-looking skin. Reverse the signs of aging and improve the overall health of your skin with DMK Skin Revision.

All DMK products are made of a blend of natural ingredients that mimic the skin’s biological processes. Keeping ingredients as close to your skin’s natural biochemistry as possible allows your skin to respond more favorably to treatments and embrace your treatment plan as a natural solution to problems with your skin.

DMK Skin Revision works by addressing exactly what your skin chemistry needs at the time of your consultation and treatment plan. DMK uses enzyme treatment to achieve desired results. These enzymes aim to strengthen the structural integrity of your skin and create a healthy environment that detoxifies and teaches your skin to embrace collagen production while improving elasticity, all of which will brighten and firm up your skin. 

All of this is achieved with a formulated range of treatment plans based on your skin’s biochemistry.

After a DMK Skin Revision treatment, most will see immediate results, leaving their provider’s office looking fresh-faced and rejuvenated. For long-lasting results and to address the root cause of your skin issues, like acne, redness and fine lines, you’ll want to follow the treatment plan recommended to you by your provider.

You’ll be teaching your skin how to respond to adversity moving forward, including how to bump up collagen production and maintain a more vibrant appearance.

How often you get a DMK facial will depend on your skin type and treatment plan. Most benefit from DMK enzyme facial treatments every week or so, besides regular treatments at home to maintain results and protect your skin.

As DMK Skin Revision treatments are individualized based on your skin’s unique needs, how much your DMK will cost will depend on that treatment plan. Our staff at the Med Lounge in Orange County can help you come up with packages that make sense for your skin’s needs and your personal goals for feeling your best.

What to Expect With DMK Skin Revision

For the best results and to reduce the chance of any side effects after your treatment, our experts at the Med Lounge have a few tips around what to expect with DMK Skin Revision before and after your procedure.

PRE-TREATMENT

  • Come to your appointments early to leave time for skincare consultations. Your provider will want to know your goals for your treatment that day and any progress reports if this is not your first treatment in your series.
  • Dress comfortably. You’ll need to put on a drape if your treatment plan for the day involves enzyme therapy, so it’s best to come in loose clothing.
  • Arrive at your appointment fresh-faced. That means no makeup and no topical creams. Your provider would remove anything you’ve applied anyway ahead of your treatment, as the first step involves cleansing your skin.
  • Avoid a blowout the morning of your appointment, too. We’ll do our best to keep your hair looking fresh, but it’s not unheard of to get some product in your hair during a treatment. Your skin is the focus here.
  • Prepare to relax. Treatments can take up to 2 hours, depending on what’s on the agenda that day. 
  • Depending on your treatment that day, you may expect some tightness or minor discomfort. This is normal and a signal that the treatment is doing its work to detoxify your skin. If discomfort increases or you feel a burning sensation during treatment, let your provider know immediately.

POST-TREATMENT

  • There is no downtime with most DMK Skin Revision treatments. The goal is to have you looking dewy and fresh at the end of your session.
  • Avoid extensive sun exposure in the days following your treatment. If you have to spend time outside, make sure to apply a protective sunscreen.
  • How long you can expect your results to last depends on where you are in your treatment plan and whether you’re also using regular at-home prescriptives. Longevity improves with a regular treatment plan and treating your new skin right. 
  • Your provider will have recommendations for a regular series of treatments to address your skin’s ills. Following your treatment plan as recommended will include time for the skin to heal and rebuild and maintain the beautiful results you’ll see after your treatments.
  • Your provider will also have recommendations for home prescriptions at the end of your treatment. Follow your treatment plan to not only maintain your glowing results but to continue teaching your skin how to look and feel its best.
  • Some dryness or tightness in targeted areas is typical after a treatment but will go away as your skin’s health improves. You may experience an acne outbreak due to bringing those impurities to the surface, but this is all a part of teaching your skin how to react to the treatments. Contact your provider if you experience any pain, itching, burning or skin pigmentation following a treatment. 

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BOTOX® Cosmetic (onabotulinumtoxinA) Important Information

 

Indications

BOTOX® Cosmetic (onabotulinumtoxinA) is indicated in adult patients for the temporary improvement in the appearance of:

– Moderate to severe glabellar lines associated with corrugator and/or procerus muscle activity

– Moderate to severe lateral canthal lines associated with orbicularis oculi activity

 

– Moderate to severe forehead lines associated with frontalis activity

 

IMPORTANT SAFETY INFORMATION, INCLUDING BOXED WARNING

 

WARNING: DISTANT SPREAD OF TOXIN EFFECT

Postmarketing reports indicate that the effects of BOTOX® Cosmetic and all botulinum toxin products may spread from the area of injection to produce symptoms consistent with botulinum toxin effects. These may include asthenia, generalized muscle weakness, diplopia, ptosis, dysphagia, dysphonia, dysarthria, urinary incontinence, and breathing difficulties. 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 treated for spasticity and other conditions, particularly in those patients who have an underlying condition that would predispose them to these symptoms. In unapproved uses and approved indications, cases of spread of effect have been reported at doses comparable to those used to treat cervical dystonia and spasticity and at lower doses.

CONTRAINDICATIONS

BOTOX® Cosmetic is contraindicated in the presence of infection at the proposed injection site(s) and in individuals with known hypersensitivity to any botulinum toxin preparation or to any of the components in the formulation.

WARNINGS AND PRECAUTIONS

Lack of Interchangeability Between Botulinum Toxin Products

The potency units of BOTOX® Cosmetic are specific to the preparation and assay method utilized. They are not interchangeable with other preparations of botulinum toxin products and, therefore, units of biological activity of BOTOX® Cosmetic cannot be compared to nor converted into units of any other botulinum toxin products assessed with any other specific assay method.

Spread of Toxin Effect

Please refer to Boxed Warning for Distant Spread of Toxin Effect.

No definitive serious adverse event reports of distant spread of toxin effect associated with dermatologic use of BOTOX® Cosmetic at the labeled dose of 20 Units (for glabellar lines), 24 Units (for lateral canthal lines), 40 Units (for forehead lines with glabellar lines), 44 Units (for simultaneous treatment of lateral canthal lines and glabellar lines), and 64 Units (for simultaneous treatment of lateral canthal lines, glabellar lines, and forehead lines) have been reported. Patients or caregivers should be advised to seek immediate medical care if swallowing, speech, or respiratory disorders occur.

Serious Adverse Reactions With Unapproved Use

Serious adverse reactions, including excessive weakness, dysphagia, and aspiration pneumonia, with some adverse reactions associated with fatal outcomes, have been reported in patients who received BOTOX® injections for unapproved uses. In these cases, the adverse reactions were not necessarily related to distant spread of toxin, but may have resulted from the administration of BOTOX® to the site of injection and/or adjacent structures. In several of the cases, patients had pre-existing dysphagia or other significant disabilities. There is insufficient information to identify factors associated with an increased risk for adverse reactions associated with the unapproved uses of BOTOX®. The safety and effectiveness of BOTOX® for unapproved uses have not been established.

Hypersensitivity Reactions

Serious and/or immediate hypersensitivity reactions have been reported. These reactions include anaphylaxis, serum sickness, urticaria, soft-tissue edema, and dyspnea. If such reactions occur, further injection of BOTOX® Cosmetic should be discontinued and appropriate medical therapy immediately instituted. One fatal case of anaphylaxis has been reported in which lidocaine was used as the diluent and, consequently, the causal agent cannot be reliably determined.

Cardiovascular System

There have been reports following administration of BOTOX® of adverse events involving the cardiovascular system, including arrhythmia and myocardial infarction, some with fatal outcomes. Some of these patients had risk factors including pre-existing cardiovascular disease. Use caution when administering to patients with pre-existing cardiovascular disease.

Increased Risk of Clinically Significant Effects With Pre-existing Neuromuscular Disorders

Individuals with peripheral motor neuropathic diseases, amyotrophic lateral sclerosis, or neuromuscular junction disorders (eg, myasthenia gravis or Lambert-Eaton syndrome) should be monitored when given botulinum toxin. Patients with neuromuscular disorders may be at increased risk of clinically significant effects including generalized muscle weakness, diplopia, ptosis, dysphonia, dysarthria, severe dysphagia, and respiratory compromise from onabotulinumtoxinA (see Warnings and Precautions).

Dysphagia and Breathing Difficulties

Treatment with BOTOX® 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. In most cases, this is a consequence of weakening of muscles in the area of injection that are involved in breathing or oropharyngeal muscles that control swallowing or breathing (see Boxed Warning).

Pre-existing Conditions at the Injection Site

Caution should be used when BOTOX® Cosmetic treatment is used in the presence of inflammation at the proposed injection site(s) or when excessive weakness or atrophy is present in the target muscle(s).

Dry Eye in Patients Treated With BOTOX® Cosmetic

There have been reports of dry eye associated with BOTOX® Cosmetic injection in or near the orbicularis oculi muscle. If symptoms of dry eye (eg, eye irritation, photophobia, or visual changes) persist, consider referring patients to an ophthalmologist.

Human Albumin and Transmission of Viral Diseases

This product contains albumin, a derivative of human blood. 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 Creutzfeldt-Jakob 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 identified for licensed albumin or albumin contained in other licensed products.

ADVERSE REACTIONS

The most frequently reported adverse reactions following injection of BOTOX® Cosmetic for glabellar lines were eyelid ptosis (3%), facial pain (1%), facial paresis (1%), and muscular weakness (1%).

The most frequently reported adverse reaction following injection of BOTOX® Cosmetic for lateral canthal lines was eyelid edema (1%).

The most frequently reported adverse reactions following injection of BOTOX® Cosmetic for forehead lines with glabellar lines were headache (9%), brow ptosis (2%), and eyelid ptosis (2%).

DRUG INTERACTIONS

Co-administration of BOTOX® Cosmetic and aminoglycosides or other agents interfering with neuromuscular transmission (eg, curare-like compounds) should only be performed with caution as the effect of the toxin may be potentiated. Use of anticholinergic drugs after administration of BOTOX® Cosmetic may potentiate systemic anticholinergic effects.

The effect of administering different botulinum neurotoxin 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.

Excessive weakness may also be exaggerated by administration of a muscle relaxant before or after administration of BOTOX® Cosmetic.

USE IN SPECIFIC POPULATIONS

There are no studies or adequate data from postmarketing surveillance on the developmental risk associated with use of BOTOX® Cosmetic in pregnant women. There are no data on the presence of BOTOX® Cosmetic in human or animal milk, the effects on the breastfed child, or the effects on milk production.

 

Please see BOTOX® Cosmetic full Prescribing Information including Boxed Warning and Medication Guide.

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