Different products for your distinctive needs

Many leading nonsurgical products to help address concerns with your appearance are part of the Brilliant Distinctions® Program. Scroll down to learn more and see the before-and-after journeys of people treated with some of these products.

UPPER
MID
LOWER
SKIN

Discover different treatment options for you

Select a facial area to learn how your aesthetic specialist can treat these areas to improve their look.

The safety and efficacy of these products for combined use have not been studied.

MODERATE TO SEVERE FROWN LINES AND CROW’S FEET

BOTOX® Cosmetic targets one of the underlying causes of frown lines and crow’s feet—the repeated muscle contractions from frowning and squinting over the years.

BOTOX® Cosmetic is the only FDA-approved treatment to temporarily improve the look of both moderate to severe crow’s feet lines and frown lines between the eyebrows in adults. It targets one of the underlying causes of these deepening lines to create a smoothing effect that’s subtle.

Please see Approved Uses and Important Safety Information about BOTOX® Cosmetic, including Boxed Warning, below.

INADEQUATE OR NOT ENOUGH LASHES

LATISSE® is an FDA-approved treatment to grow eyelashes for people with inadequate or not enough lashes. As early as 4 weeks, you may see longer lashes, and enjoy the full effect of longer, fuller, and darker lashes by 16 weeks.

Please see Approved Uses and Important Safety Information about LATISSE® below.

The safety and efficacy of these products for combined use have not been studied.

MIDFACE VOLUME LOST TO AGING

As you age, your cheeks flatten, and the skin may begin to sag. This is caused by loss of fullness, or what the experts call age-related midface volume loss.

JUVÉDERM VOLUMA® XC injectable gel instantly adds volume to the cheek area to correct age-related volume loss in adults over 21. It’s the only HA filler proven to last up to 2 years.*

*With optimal treatment. Results may vary.

Please see Approved Uses and Important Safety Information about JUVÉDERM VOLUMA® XC below.

PROMINENT WRINKLES AND FOLDS AROUND THE NOSE AND MOUTH

Age, genetics, and environmental factors like sun and smoking can cause visible wrinkles and folds to appear, like the “parentheses” and corner lines around your mouth.

JUVÉDERM® XC instantly smooths moderate to severe wrinkles and folds around your nose and mouth. It’s the only HA filler proven to last up to 1 year in wrinkles and folds.*

*With optimal treatment. Results may vary.

Please see Approved Uses and Important Safety Information about JUVÉDERM® XC below.

LIP AUGMENTATION AND VERTICAL LIP LINES

Wishing you could add subtle volume to your lips, or soften the vertical lines above them? JUVÉDERM VOLBELLA® XC makes a difference with long-lasting results.

JUVÉDERM VOLBELLA® XC is the first and only FDA-approved filler proven to increase lip fullness and soften the appearance of vertical lip lines for up to 1 year.*

*With optimal treatment. Results may vary.

Please see Approved Uses and Important Safety Information about JUVÉDERM VOLBELLA® below.

Whether you’ve noticed your lips thinning over time, or simply want fuller lips, JUVÉDERM® Ultra XC injectable gel can give you natural-looking results that last up to 1 year.*

JUVÉDERM® Ultra XC gel is for lip augmentation in adults over 21.

*With optimal treatment. Results may vary.

Please see Approved Uses and Important Safety Information about JUVÉDERM® Ultra XC below.

SUBMENTAL FULLNESS DUE TO SUBMENTAL FAT

Submental fullness, also commonly called a “double chin,” may be caused by several factors, such as weight gain, genetics, and aging. Sometimes, even with diet and exercise, the unwanted fullness beneath your chin simply won’t go away.

KYBELLA® is the only FDA-approved injectable treatment for adults that destroys fat cells in the treatment area under the chin to improve your profile—whether you have a moderate amount of chin fullness or a bit more.

Please see Approved Uses and Important Safety Information about KYBELLA® below.

The safety and efficacy of these products for combined use have not been studied.

ROUGH TEXTURE/UNEVEN SKIN TONE AND DULLNESS/FINE LINES AND WRINKLES

Has your skin lost its youthful glow? Over time, your skin’s appearance may change with the formation of fine lines and wrinkles, as well as brown spots.

SkinMedica® is science that makes beauty a reality. This line of innovative skin care products supports your skin’s ability to restore itself to deliver remarkable results.

SkinMedica® is a physician-dispensed, cosmetic, and nonprescription skin care product line.

See results

In the stories below, you’ll see the journeys of 5 different people. Each person’s recommended treatment included products featured in the Brilliant Distinctions® Program.

Check out their photos to see the differences between before and their exciting after reveal.

Brilliant Distinctions® Program

BEGIN YOUR JOURNEY TODAY AND SAVE >

Know the difference

Watch Dr. Tina Alster explain how different aesthetic treatments work at this exclusive Town & Country Magazine event.

Special savings for you

The Brilliant Distinctions® rewards add up when you receive treatments in our portfolio of products.

Did you know?

The Natrelle® Collection of breast implants is part of the Brilliant Distinctions® Program too.
Ever considered breast augmentation?

Approved Uses, Important Safety Information, and Prescribing Information

BOTOX® Cosmetic (onabotulinumtoxinA) Important Information

IMPORTANT SAFETY INFORMATION

BOTOX® Cosmetic 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 BOTOX® Cosmetic:

BOTOX® Cosmetic dosing units are not the same as, or comparable to, any other botulinum toxin product.

There has not been a confirmed serious case of spread of toxin effect when BOTOX® Cosmetic has been used at the recommended dose to treat frown lines, crow’s feet lines, or both at the same time.

BOTOX® Cosmetic may cause loss of strength or general muscle weakness, vision problems, or dizziness within hours to weeks of taking BOTOX® Cosmetic. If this happens, do not drive a car, operate machinery, or do other dangerous activities.

Serious and/or immediate allergic reactions have been reported. They include: itching, rash, red itchy welts, wheezing, asthma symptoms, or dizziness or feeling faint. Get medical help right away if you are wheezing or have asthma symptoms, or if you become dizzy or faint.

Do not take BOTOX® Cosmetic if you: are allergic to any of the ingredients in BOTOX® Cosmetic (see Medication Guide for ingredients); had an allergic reaction to any other botulinum toxin product such as Myobloc® (rimabotulinumtoxinB), Dysport® (abobotulinumtoxinA), or Xeomin® (incobotulinumtoxinA); have a skin infection at the planned injection site.

Tell your doctor about all your muscle or nerve conditions, such as ALS or Lou Gehrig’s disease, myasthenia gravis, or Lambert-Eaton syndrome, as you may be at increased risk of serious side effects including difficulty swallowing and difficulty breathing from typical doses of BOTOX® Cosmetic.

Tell your doctor about all your medical conditions, including: plans to have surgery; had surgery on your face; weakness of forehead muscles: trouble raising your eyebrows; drooping eyelids; any other abnormal facial change; are pregnant or plan to become pregnant (it is not known if BOTOX® Cosmetic can harm your unborn baby); are breast-feeding or plan to (it is not known if BOTOX® Cosmetic passes into breast milk).

Tell your doctor about all the medicines you take, including prescription and nonprescription medicines, vitamins, and herbal products. Using BOTOX® Cosmetic with certain other medicines may cause serious side effects. Do not start any new medicines until you have told your doctor that you have received BOTOX® Cosmetic in the past.

Tell your doctor if you have received any other botulinum toxin product in the last 4 months; have received injections of botulinum toxin such as Myobloc®, Dysport®, or Xeomin® in the past (tell your doctor exactly which product you received); have recently received an antibiotic by injection; take muscle relaxants; take an allergy or cold medicine; take a sleep medicine; take aspirin-like products or blood thinners.

Other side effects of BOTOX® Cosmetic include: discomfort or pain at the injection site; headache; and eye problems: double vision, blurred vision, drooping eyelids, and swelling of your eyelids.

For more information refer to the Medication Guide or talk with your doctor.

To report a side effect, please call Allergan at 1-800-678-1605.

Approved Uses

BOTOX® Cosmetic is a prescription medicine that is injected into muscles and used to temporarily improve the look of both moderate to severe crow’s feet lines and frown lines between the eyebrows in adults.

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

LATISSE® (bimatoprost ophthalmic solution) 0.03% Important Information

Approved Use

LATISSE® is an FDA-approved treatment to grow eyelashes for people with inadequate or not enough lashes.

Important Safety Information

If you use/used prescription products for eye pressure problems, use LATISSE® under doctor care. May cause brown darkening of the colored part of the eye which is likely permanent. LATISSE® may cause eyelid skin darkening which may be reversible. Only apply at base of upper lashes. DO NOT APPLY to lower lid. Hair may grow outside the treatment area. If you have eye problems/surgery, consult your doctor. Common side effects include itchy and red eyes. If discontinued, lashes gradually return to previous appearance.

To report a side effect, please call Allergan at 1-800-678-1605.

Please see LATISSE® full Prescribing Information.

KYBELLA® (deoxycholic acid) injection 10 mg/mL Important Information

Approved Use

KYBELLA is a prescription medicine used in adults to improve the appearance and profile of moderate to severe fat below the chin (submental fat), also called “double chin.”

It is not known if KYBELLA is safe and effective for use outside of the submental area or in children less than 18 years of age.

IMPORTANT SAFETY INFORMATION

Who should not receive KYBELLA?

You should not receive KYBELLA if you have an infection in the treatment area.

Before receiving KYBELLA, tell your healthcare provider about all of your medical conditions, including if you: Have had or plan to have surgery on your face, neck, or chin; have had cosmetic treatments on your face, neck, or chin; have had or have medical conditions in or near the neck area; have had or have trouble swallowing; have bleeding problems; are pregnant or plan to become pregnant (it is not known if KYBELLA will harm your unborn baby); are breastfeeding or plan to breastfeed (it is not known if KYBELLA passes into your breast milk; talk to your healthcare provider about the best way to feed your baby if you receive KYBELLA).

Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. Especially tell your healthcare provider if you take a medicine that prevents the clotting of your blood (antiplatelet or anticoagulant medicine).

What are the possible side effects of KYBELLA?

KYBELLA can cause serious side effects, including nerve injury in the jaw (which can cause an uneven smile or facial muscle weakness), or trouble swallowing.

The most common side effects of KYBELLA include swelling, bruising, pain, numbness, redness, and areas of hardness in the treatment area.

These are not all of the possible side effects of KYBELLA. Call your healthcare provider for medical advice about side effects.

Please see KYBELLA® full Prescribing Information.

CoolSculpting® Treatment Important Information

The CoolSculpting® procedure is FDA-cleared for the treatment of visible fat bulges in the submental area, thigh, abdomen and flank, along with bra fat, back fat, underneath the buttocks (also known as banana roll), and upper arm. Please talk to your healthcare provider or see full Important Safety Information for additional information.

JUVÉDERM® Injectable Gel Fillers Important Information

Approved Uses

JUVÉDERM VOLUMA® XC injectable gel is for deep injection in the cheek area to correct age-related volume loss in adults over 21.

JUVÉDERM® XC and JUVÉDERM VOLLURE™ XC injectable gels are for injection into the facial tissue for the correction of moderate to severe facial wrinkles and folds, such as nasolabial folds. JUVÉDERM VOLLURE™ XC injectable gel is for adults over 21.

JUVÉDERM® Ultra XC is for injection into the lips and perioral area for lip augmentation in adults over 21.

JUVÉDERM VOLBELLA® XC injectable gel is for injection into the lips for lip augmentation and for correction of perioral lines in adults over 21.

IMPORTANT SAFETY INFORMATION

Are there any reasons why I should not receive any JUVÉDERM® injectable gel formulation?

Do not use these products if you have a history of multiple severe allergies or severe allergic reactions (anaphylaxis), or if you are allergic to lidocaine or the Gram-positive bacterial proteins used in these products.

What precautions should my doctor advise me about?

What are possible side effects?

The most commonly reported side effects with JUVÉDERM® injectable gels included injection-site redness, swelling, pain, tenderness, firmness, lumps/bumps, bruising, discoloration, and itching. For JUVÉDERM VOLBELLA® XC, dryness was also reported. For JUVÉDERM VOLUMA® XC, most side effects were moderate and lasted 2 to 4 weeks. For JUVÉDERM® XC, JUVÉDERM VOLLURE™ XC, and JUVÉDERM® Ultra XC injectable gels, most side effects were mild or moderate and lasted 14 days or less. For JUVÉDERM VOLBELLA® XC, most side effects were mild or moderate and lasted 30 days or less.

One of the risks with using these products is unintentional injection into a blood vessel, and, while rare, the complications can be serious and may be permanent. These complications, which have been reported for facial injections, can include vision abnormalities, blindness, stroke, temporary scabs, or permanent scarring.

As with all skin injection procedures, there is a risk of infection.

To report a side effect with any JUVÉDERM® product, please call Allergan at 1-800-433-8871. Please visit Juvederm.com or talk to your doctor for more information.

Available by prescription only.

Natrelle® Breast Implants Important Information

Who may get breast implants?

Natrelle® Breast Implants are approved for women for the following:

Breast augmentation includes primary breast augmentation to increase breast size, as well as revision surgery to correct or improve the result of a primary breast augmentation surgery.

IMPORTANT SAFETY INFORMATION

Who should NOT get breast implants?

What should I know before getting breast implants?

What should I tell my doctor?

Tell your doctor if you have any of the following conditions, as the risk of breast implant surgery may be higher:

What are some complications with breast implants?

Key complications are reoperation, implant removal with or without replacement, implant rupture with silicone-filled implants, implant deflation with saline-filled implants, and severe capsular contracture (severe scar tissue around the implant). Other complications include asymmetry, nipple/breast/skin sensation changes, scarring, or wrinkling/rippling. Talk to your doctor about other complications.

Talk to your doctor. For more information or to report a problem with Natrelle® Breast Implants, please call Allergan at 1-800-433-8871. Please also see the patient brochures at www.allergan.com/labeling/usa.html.

Natrelle® Breast Implants are available by prescription only.

REVOLVE™ Advanced Adipose System

Important Safety Considerations for REVOLVE™ System

REVOLVE™ System is a single use, sterile, disposable canister that is intended for processing, filtering, and transferring of autologous adipose tissue. The device is intended to be used by a plastic surgeon to perform autologous fat grafting in aesthetic body contouring procedures.

Autologous fat grafting should not be performed in the presence of any disease process that adversely affects wound healing, and in patients who are in poor overall health. Some common adverse effects associated with autologous fat transfer are asymmetry, over- and/or under correction of the treatment site, tissue lumps, bleeding, and scarring.

Every patient’s situation is different, so be sure to ask your surgeon if the use of REVOLVE™ System is right for you. This brochure is not intended to replace a patient’s discussion with a surgeon. It does not describe all the potential risks and potential benefits associated with fat grafting procedures.

REVOLVE™ System is available only through licensed plastic surgeons. Complete product and safety information is available at lifecell.com.

SkinMedica®

Most of the SkinMedica® products described on this website are intended to meet the FDA’s definition of a cosmetic product, an article applied to the human body to cleanse, beautify, promote attractiveness, and alter appearances. These SkinMedica® products are not intended to be drug products that diagnose, treat, cure, or prevent any disease or condition. These products have not been approved by the FDA, and the statements on these pages have not been evaluated by the FDA.

SkinMedica® Total Defense + Repair Broad Spectrum Sunscreens (SPF 34, SPF 34 Tinted, and SPF 50+), Essential Defense Broad Spectrum Sunscreens (Everyday Clear SPF 47, Mineral Shield Tinted SPF 32, and Mineral Shield SPF 35), SkinMedica Daily Physical Defense® Sunscreen Broad Spectrum SPF 30+, Environmental Defense Sunscreen™ SPF 50+ with UV ProPlex™, and TNS Ultimate Daily Moisturizer™ SPF 20 Sunscreen are over-the-counter drug products which are formulated and marketed pursuant to FDA’s governing regulations set forth at 21 C.F.R. Part 352.

SkinMedica® Acne System, Acne Treatment Lotion, Purifying Foaming Wash, and Purifying Toner, are over-the-counter drug products which are formulated and marketed pursuant to FDA’s governing regulations set forth at 21 C.F.R. § 333.301 et seq.

Approved Uses and Important Safety Information

BOTOX® Cosmetic (onabotulinumtoxinA) Important Information

IMPORTANT SAFETY INFORMATION

BOTOX® Cosmetic 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 BOTOX® Cosmetic:

  • 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 including: 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, trouble swallowing