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CoolSculpting Elite in Orange County

CoolSculpting Elite in Orange County

Target & Reduce

CoolSculpting Elite is the upgrade to CoolSculpting, a technology that uses a process called cryolipolysis to freeze fat cells in areas that refuse to cooperate with traditional diet and exercise. This non-invasive, non-surgical body contouring procedure essentially sucks fat cells into a vacuum, never to be heard from again once they’re frozen, broken down and eliminated. What’s left behind is a slimmer, trimmer you, all thanks to the power of the deep freeze.

CoolSculpting Elite is the ideal treatment for those that are oh-so-close to their body goals and already at or near their goal weight. It’s for men and women who want to trim up those love handles, give their booties a lift by reducing fat on their backsides, or slimming down their upper arms once and for all. It also works on belly fat, double chins and fat reduction in the thighs. 

Are you ready to try CoolSculpting in Orange County? Our Med Lounge staff is waiting to share what we can do, even if you’re looking to target multiple areas at a time. Ask about our Elite upgrade if that’s what you’re after. That beach body is waiting.

Benefits of CoolSculpting Elite


Proven fat loss

Safe and effective

Targeted fat reduction

Fat cells are permanently gone

Treat multiple areas at a time

Noticeable results

Zero downtime

Minimal discomfort

Confidence boost

Frequently Asked Questions

CoolSculpting Elite uses a process called cryolipolysis to freeze fat cells in targeted areas of the body. It is an upgrade to its predecessor, CoolSculpting, promising a more efficient, comprehensive process that reduces fat more quickly and over a larger surface area.

Yes, CoolSculpting works! It’s a non-invasive treatment to target problem areas in a safe, effective way. Those fat cells are also gone for good once they’re frozen, leaving you with an overall fat reduction of an average of 20% in targeted areas. 

CoolSculpting Elite works best for men and women who have been unable to reduce fat in stubborn areas through traditional diet and exercise. The treatment is not a weight-loss tool but a body contouring procedure to trim and reduce fat in targeted areas. It works best with those who are at or close to their ideal weight but are having difficulties with targeted fat reduction.

The treatment is most often used in nine areas of the body, all cleared by the FDA: the inner and outer thighs, belly, underneath the buttocks, upper arms, love handles and anywhere along your flank, excess fat along the bra straps, and underneath the chin.

Women who are pregnant or thinking about becoming pregnant, have chronic fatigue or an autoimmune disease or have had injuries or previous surgeries in the targeted areas are not candidates for CoolSculpting sessions. 

If you’re just not sure whether the treatment is right for you, contact our experts at the Med Lounge for a free CoolSculpting consultation. They’ll go over your options with you, even if that means coming up with an alternative treatment that’s a better fit for your body goals.

The cost of your CoolSculpting treatment plan will depend on how many treatments you elect to have. Your provider will talk you through your options and help you decide how many treatments you’ll need to achieve your desired results. Some patients will want to target multiple areas with CoolSculpting, especially after they’ve seen fat reduction improvements after just one session. 

Our experts at Med Lounge can work within your budget to recommend a plan to help you reach your body goals.

CoolSculpting works by attaching a device to treatment areas that essentially works like a vacuum, sucking up the top layer of skin into the Elite applicator. CoolSculpting Elite allows for dual applicators simultaneously, which means you can target two problem areas in one session for maximum efficiency.

It sounds like science fiction, but the procedure itself is actually based on proven science behind freezing fat cells. That means you’ll likely feel some cold at targeted areas, along with some pulling and tugging. Throughout your treatment, which can last up to an hour depending on targeted areas, the site will numb quite a bit from the cooling properties of the treatment. 

Some patients report some discomfort after the treatment, not unlike an intense workout in the gym. Your provider will massage the area after your treatment to relieve some of that discomfort and maximize the procedure’s effectiveness.

Most patients see a fat reduction in the 20% range in treated areas targeted by CoolSculpting treatments. Some may see even more impressive results in the 25% range. It’s a safe, effective tool that permanently reduces fat cells in areas that can be difficult to address with diet and exercise alone.

See the amazing difference in our clients, before and after treatment.

Click the image to see an enlarged preview.

What to Expect With CoolSculpting Elite

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 CoolSculpting before and after your procedure.


  • Follow a regular exercise and healthy diet routine before your treatments. The best candidates for CoolSculpting Elite are at or near their goal weight and in good health.
  • Wear loose, comfortable clothing to your CoolSculpting Elite appointment. Your provider will need easy access to areas being treated by the device.
  • Drink plenty of water before your appointment so that you aren’t dehydrated. This will improve elasticity in the skin and kick your metabolism into gear.
  • Remove any jewelry and put away electronic devices before starting your treatment. 
  • A light meal is fine before treatment. Try to avoid large meals or foods that can increase bloating, including processed foods or salty items.
  • Talk to your provider about any conditions you have or any injuries or surgeries you’ve experienced in the areas you’d like to target. Your provider will be able to tell you whether CoolSculpting Elite is safe for you or whether you’re a better candidate for a different kind of treatment. 


  • There is no expected downtime after a CoolSculpting Elite session. You’ll be able to resume normal activities after your treatment. 
  • The recommended number of sessions for optimal results will depend on the areas you’re targeting, but most patients schedule anywhere from one to 3 sessions. Schedule your sessions as recommended by your provider at the end of your CoolSculpting Elite appointment, and follow treatment instructions to the letter. 
  • It is recommended that you schedule a follow-up appointment a few months after your final session so that you and your provider can take a look at your results at that time and schedule additional treatments if needed.
  • Regular exercise and a healthy eating plan will go a long way in extending your results. Weight gain doesn’t mean those frozen fat cells will return to treatment areas, but it doesn’t mean you’re immune from fat cells congregating in other regions. 
  • After a session, cramping, soreness, or sensitivity at the treatment site is normal and should go away within a few days. Your skin may feel cool to the touch after your treatments. This is also normal.
  • Talk to your provider if you’re experiencing any severe symptoms after your session, such as lumps or bumps underneath the skin or severe pain that won’t go away at the treatment site. Some cramping or muscle soreness is normal but should go away within a few days after treatment.

CoolSculpting® and CoolSculpting® Elite are FDA-cleared for the treatment of visible fat bulges in the submental (under the chin) and submandibular (under the jawline) areas, thigh, abdomen, and flank, along with bra fat, back fat, underneath the buttocks (also known as banana roll), and upper arm. It is also FDA-cleared to affect the appearance of lax tissue with submental area treatments. CoolSculpting® and CoolSculpting® Elite are not treatments for weight loss.

Important Safety Information
These procedures are not for everyone. You should not be treated with CoolSculpting® or CoolSculpting® Elite if you suffer from cryoglobulinemia, cold agglutinin disease, or paroxysmal cold hemoglobinuria.

Tell your doctor if you have any medical conditions including recent surgery, pre-existing hernia, and any known sensitivities or allergies.

During the procedure you may experience sensations of pulling, tugging, mild pinching, intense cold, tingling, stinging, aching, and cramping at the treatment site. These sensations subside as the area becomes numb. Following the procedure, typical side effects include temporary redness, swelling, blanching, bruising, firmness, tingling, stinging, tenderness, cramping, aching, itching, or skin sensitivity, and sensation of fullness in the back of the throat after submental or submandibular area treatment.
Rare side effects may also occur. CoolSculpting® and CoolSculpting® Elite may cause a visible enlargement in the treated area, which may develop 2 to 5 months after treatment and requires surgical intervention for correction.

Please see CoolSculpting® full Important Safety Information and CoolSculpting® Elite full Important Safety Information for additional information.

Patient Results May Vary.

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BOTOX® Cosmetic (onabotulinumtoxinA) Important Information



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





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.


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.


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.


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%).


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.


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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