Frequently Asked Questions

You can earn points and redeem coupons for the following Allergan products and treatments:

  • BOTOX® Cosmetic (onabotulinumtoxinA)
  • JUVÉDERM® XC
  • JUVÉDERM VOLUMA® XC
  • JUVÉDERM VOLLURE XC
  • JUVÉDERM VOLBELLA® XC
  • KYBELLA® (deoxycholic acid) injection 10 mg/mL
  • SkinMedica® products
  • Natrelle® Gel Breast Implants
  • LATISSE® (bimatoprost ophthalmic solution) 0.03%

SkinMedica® products are cosmetic and nonprescription and only available through provider offices. For BOTOX® Cosmetic, points can only be earned on treatments with out-of-pocket costs greater than $200.

The program will continue to grow. The latest program news along with the most up-to-date list of ways to earn and redeem points can be found on the program website and within the Brilliant Distinctions® mobile app.

Joining is easy. You can even use your existing Facebook and Google+ credentials. You can join the program in the following ways:

  • Follow the instructions provided in the tri-fold brochure available at your provider’s office
  • Visit BrilliantDistinctionsProgram.com on any desktop computer or mobile device and click on Become a Member at the top of the homepage
  • Download the Brilliant Distinctions® mobile app and follow the registration prompts

Once registered, there are many ways you can access your account.

  • Visit BrilliantDistinctionsProgram.com on any desktop computer or mobile device and click on Sign In at the top of the homepage
  • Download the Brilliant Distinctions® mobile app and follow the log-in prompts

To find a participating provider, visit BrilliantDistinctionsProgram.com and click on Find a Doctor in the navigation.

Not all providers carry all of the participating products. Contact the provider for more information on their products and participation in the program.

Yes, log on to BrilliantDistinctionsProgram.com and select My Profile in the drop-down menu under your username and icon. You will be able to select a preferred provider or change your existing preferred provider in the Account Details section. Note: you must be a Brilliant Distinctions® member to store your provider in your profile.

No, there is no need to specify a provider. Participating providers can all redeem Brilliant Distinctions® coupons for products or treatments they qualify you for.

Each patient can have only one account, but can earn and redeem points at any participating provider.

For example, if you live in another city for part of the year, as long as the providers at both locations participate in the Brilliant Distinctions® program, points can be earned and coupons redeemed for eligible product treatments and purchases at both locations. If you have more than one account, please contact customer support at 1-888-324-2745 (9 AM-8 PM ET, M-F) and request that the profiles be merged.

Yes, points will expire 9 months from the date issued.

Points cannot be reinstated after they expire, but you will be sent an email reminding you of the date of expiration.

No information will ever be shared when donating to a charity. To make a donation you will need to acknowledge that the donation is being made by Allergan on your behalf. An email will be sent to you to confirm your donation. You can refer to www.makeawish.org and www.dressforsuccess.org for more information on the selected charity.

NOTE: Charity donations are made by Allergan on your behalf. Donations are not tax deductible.

We’d like you to let us know if this program doesn’t meet your needs, but any account can be closed online by logging on to BrilliantDistinctionsProgram.com and selecting My Profile in the drop-down menu under your username and icon. You will be able to close your account in the Account Details section by clicking on Remove My Account, under Account Actions. You may also call the customer support line at 1-888-324-2745 (9 AM-8 PM ET, M-F).

The information that you provide in connection with Brilliant Distinctions® may be used for Allergan’s business and marketing purposes and to send you information about the program and other Allergan products and services, in accordance with Allergan’s Privacy Statement and Terms of Use. By participating, you agree that Allergan may collect and use your personal information that you provide us in accordance with Allergan’s Privacy Statement and Terms of Use.

Federal government regulations (HIPAA) prevent us from allowing joint accounts.

Each individual is welcome to have their own individual program account.

This program is designed to allow all communications with members to take place via the Internet and email. Nothing will ever be sent from Brilliant Distinctions® to your home address without your permission.

No, you can go to any participating provider to receive points.

Latest program news along with the most up-to-date list of ways to earn and redeem points can be easily found on the program website. You can

  • View currently running promotions on your dashboard in the Current Offers section once logged in
  • View our Points Earning Guide for a list of participating products and their Brilliant Distinctions® points values

My Rewards History only tracks transactions made through the Brilliant Distinctions® Program and is not meant to be used as an electronic recording system for your health records. Please see your provider for records beyond the transactions made in Brilliant Distinctions®.

The Brilliant Distinctions® Mall allows you to shop at popular online retailers and earn Brilliant Distinctions® points redeemable for participating Allergan treatments and products.
  • Once a purchase is made, it will show in your Rewards History as pending for 45 days. After 45 days, your points will show as issued and available for use
  • If you return your Brilliant Distinctions® Mall purchase, those points will be removed from your account

Promotions may occur regularly and will often utilize the Brilliant Distinctions® program for processing. Please refer to the information and rules that are provided with the promotion.

You can earn points towards future savings at participating providers on each BOTOX® Cosmetic, JUVÉDERM® XC, JUVÉDERM VOLUMA® XC, JUVÉDERM VOLLURE XC, or JUVÉDERM VOLBELLA® XC  treatment, or KYBELLA® (deoxycholic acid) injection 10 mg/mL, every LATISSE®  or SkinMedica® purchase, and any Natrelle® Gel Breast Implants. Only your doctor can determine which products and treatments are right for you.

SEE EARNINGS GUIDE

Since injection intervals of BOTOX® (onabotulinumtoxinA) Cosmetic should be no more frequent than every 3 months, you will not be awarded points for a BOTOX® Cosmetic treatment less than 3 months from your last treatment. Since treatments with KYBELLA® (deoxycholic acid) injection 10mg/mL should be no more frequent than once a month, receiving a treatment less than one month from your last treatment or more than 7 total single treatments will not result in awarded points. Points are awarded for only one breast augmentation procedure with Natrelle® Gel Breast Implants. There are no restrictions on the frequency of JUVÉDERM® XC, JUVÉDERM VOLUMA® XC, JUVÉDERM VOLLURE XC, or JUVÉDERM VOLBELLA® XC treatments, or the purchase of LATISSE® or SkinMedica® skin care products.

Points will be issued by the provider for each treatment and purchase. At the end of the transaction, an itemized list of the point breakdown will be displayed in the Rewards History tab of your profile on the program website or mobile app.

Your provider must issue points for a treatment or product purchase. Points will be deposited into your account within 2-3 days after your provider has issued them. You can utilize the earned points as early as your next treatment or purchase.

Due to Federal regulations, points are non-transferable.

No, points will automatically be added to your account within 2-3 days of the point issuance.

Points can be redeemed for coupons. You may create coupons based upon your earned points and present that coupon to a participating Brilliant Distinctions® provider to redeem for savings on qualifying treatments.

Points Redeem For
100 POINTS = $10
200 POINTS = $20
300 POINTS = $30
400 POINTS = $40
500 POINTS = $50
Points Redeem For
600 POINTS = $60
700 POINTS = $70
800 POINTS = $80
900 POINTS = $90
1000 POINTS = $100

Coupons can be created for a maximum amount of $100.

Yes, when you create a coupon, it is issued with an expiration date of 60 days. It is best to wait until a treatment is scheduled before creating a coupon.

If printing is not an option, you can either write down the coupon code listed on your created coupon, or utilize the Email Coupon function that displays after a coupon is created. This will allow you to send a message to any email address that will contain all of the information needed by the provider. If you are on a mobile device you can also download a coupon to your mobile wallet from either the mobile website or the Brilliant Distinctions® mobile app.

The following states may require LATISSE® to be dispensed via the pharmacy: Massachusetts, Montana, New York, Texas, and Puerto Rico.

To earn points at the pharmacy, create a Points-Earning Certificate.
  1. Log in to your account at BrilliantDistinctionsProgram.com
  2. Click on Shop and Earn in the navigation
  3. Look for the Going to the Pharmacy? callout at the bottom of the page under the Points for Treatments tab
  4. Click on Create Certificate
  5. Print the certificate, email it to yourself, or add it to your mobile wallet (if on a mobile device) and take it to the pharmacy to earn Brilliant Distinctions® points for your LATISSE® purchase

You will receive an email confirmation from us within 5-7 days of your transaction letting you know that you have earned points from your LATISSE® kit(s) purchase.

To redeem a coupon at the pharmacy, create a LATISSE® coupon.

  1. Log in to your account at BrilliantDistinctionsProgram.com
  2. Click on Create a LATISSE® Pharmacy Coupon in the coupon summary section at the top of the homepage
  3. Select the coupon amount and click Activate Coupon (Note: Pharmacy coupons can only be created for $20 or $40)
  4. Print the coupon, email it to yourself, or add it to your mobile wallet (if on a mobile device) and take it to the pharmacy for redemption

There is no need to also create a Points-Earning Certificate; the coupon will also allow you to earn points on your transaction.

There are a few steps that can be taken to correct this issue.

  1. Try to log-in using the credentials you provided at registration. If unable to sign in, it’s likely that you did not fully complete registration. Try to register again
  2. If you are able to log into your account, check your patient details to ensure they are accurate (Last Name, Birth Date, Zip Code). These are the data points that your provider will use to find you in their system
  3. You can also supply your provider with your Member ID, found on your homepage under Membership or your member card ID, found above the bar code on the back of your member card
  4. If you continue to have problems, please contact customer support at 1-888-324-2745 (9AM-8PM EST, M-F)

The points confirmation email is not necessary, but you should check to make sure your email address is correct by looking under My Profile after you have signed in.

Note: Make sure to add BrilliantDistinctions@BrilliantDistinctionsprogram.com as a safe sender to ensure these emails are being delivered.

You have the option to cancel a coupon once it’s been created.

  1. Log in to your account at BrilliantDistinctionsProgram.com
  2. At the top of the page, under the profile icon, click on My Profile
  3. Click on the Rewards History tab on the My Profile page
  4. Locate the coupon you would like to cancel within the table and click on Cancel in the Action column at the far right of your screen

Note: You cannot cancel a coupon after it has expired (60 days from creation), and your points used for the coupon will revert to their original expiration date. If that date has passed, your points will be removed.

You should cancel the coupon on the program site. See detailed instructions for canceling a coupon in the “What if I accidentally create a coupon?” FAQ above.

If additional assistance is needed, you can contact the customer support line at 1-888-324-2745 (9 AM-8 PM ET, M-F) and speak to a representative who can help issue a new coupon.

The program is only accessible through the Internet. This includes program registration and redeeming points. If you don’t personally have Internet access, we suggest that you ask if your provider has Wifi available in office, or visit either a local library or Internet café.

You do not need a member card to participate in the Brilliant Distinctions® program. We encourage all members to have one, as it speeds your check-in and –out times by helping your provider to quickly locate your account and apply your rewards accurately.

A participating Brilliant Distinctions® provider can supply you with a member card at your next visit.

To activate your member card, select the corresponding option under the Account Actions column found on your profile page. Just follow the prompts and your card will be linked to your account.

  1. Log in to your account at BrilliantDistinctionsProgram.com
  2. Click on the Welcome, Your Name message at the top of the page
  3. Click on My Profile
  4. On the Account Details tab, under Account Actions, click on Activate Member Card
  5. Enter the 9-digit number found on the back of your member card when prompted, and click Activate My Card

To download the Brilliant Distinctions® mobile app you can follow the download link found on the homepage of this website. You can also search for “Brilliant Distinctions” in the App Store® on your Apple mobile device, or the Google PlayTM Store on your Android mobile device.

No. We use your social media accounts to help identify you. We do not share any of your information, nor do we have the ability to post anything on your behalf.

Participating Products

Available by prescription only

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Available by prescription only

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Available by prescription only

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Available by prescription only

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Available by prescription only

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Physician-dispensed skin care product line

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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

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.

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

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.

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 Product 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.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.FDA.gov/safety/MedWatch or call 1-800-FDA-1088.

Please talk to your healthcare provider or see full Prescribing 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 injectable gel is 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 injection into the facial tissue for the correction of moderate to severe facial wrinkles and folds, such as nasolabial folds in adults over 21.

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

JUVÉDERM VOLBELLA® XC injectable gel is for injection into the lips for lip augmentation and for correction of perioral lines in adults over the age of 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?
  • Tell your doctor if you are pregnant or breastfeeding. The safety of these products for use during pregnancy or while breastfeeding has not been studied
  • The safety of JUVÉDERM VOLUMA® XC in patients under 35 years or over 65 years, the safety of JUVÉDERM® XC and JUVÉDERM® Ultra XC injectable gels in patients under 18 years, and the safety of JUVÉDERM VOLLURE™ XC and JUVÉDERM VOLBELLA® XC in patients under 22 years has not been studied
  • The safety and effectiveness of JUVÉDERM VOLUMA® XC in areas other than the cheek area, JUVÉDERM® XC and JUVÉDERM VOLLURE™ XC for areas other than facial wrinkles and folds, and JUVÉDERM® Ultra XC and JUVÉDERM VOLBELLA®XC in areas other than the lips and perioral area have not been established in clinical studies
  • Tell your doctor if you have a history of excessive scarring (eg, hypertrophic scarring and keloid formations) or pigmentation disorders, as use of these products may result in additional scars or changes in pigmentation
  • Tell your doctor if you are planning other laser treatments or a chemical peel, as there is a possible risk of inflammation at the treatment site if these procedures are performed after treatment
  • Patients who experience skin injury near the site of injection with this product may be at higher risk for side effects
  • Tell your doctor if you are on immunosuppressive therapy used to decrease the body’s immune response, as use of these products may result in an increased risk of infection
  • Tell your doctor if you are using medications that can prolong bleeding, such as aspirin, ibuprofen, or other blood thinners, as this may result in increased bruising or bleeding at the injection site
  • Minimize strenuous exercise, exposure to extensive sun or heat, and alcoholic beverages within the first 24 hours following treatment

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 for women at least 22 years old for silicone-filled implants.
  • Breast augmentation for women at least 18 years old for saline-filled implants.

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?
  • Women with active infection anywhere in their body.
  • Women with existing cancer or precancer of their breast who have not received adequate treatment for those conditions.
  • Women who are currently pregnant or nursing.
What should I know before getting breast implants?
  • Breast implants are not lifetime devices, and not necessarily a one-time surgery.
  • Many of the changes to your breasts following implantation cannot be undone. If you later choose to have your implant(s) removed and not replaced, you may experience unacceptable dimpling, puckering, wrinkling, or other cosmetic changes of the breast, which may be permanent.
  • Breast implants may affect your ability to breast-feed, either by reducing or eliminating milk production.
  • Rupture of a silicone-filled breast implant is most often silent and may not be detected by you or your doctor. You should have an MRI 3 years after your surgery and then every 2 years after that for as long as you have your breast implants to determine if rupture is present. If implant rupture is noted on an MRI, you should have the implant removed, with or without replacement.
  • With breast implants, a routine screening mammography and self-examinations for breast cancer will be more difficult. Ask your doctor to help you distinguish the implant from your breast tissue. Symptoms of a ruptured implant may be hard knots or lumps surrounding the implant or in the armpit, change or loss of size or shape of the breast or implant, pain, tingling, swelling, numbness, burning, or hardening. Tell your doctor of these symptoms and remove ruptured implants.
  • Inform any other doctor who treats you of the presence of your implants to minimize the risk of damage to the 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:
  • Autoimmune diseases (for example, lupus and scleroderma).
  • A weakened immune system (for example, currently taking drugs that weaken the body’s natural resistance to disease).
  • Planned chemotherapy following breast implant placement.
  • Planned radiation therapy to the breast following breast implant placement.
  • Conditions or medications that interfere with wound healing and blood clotting.
  • Reduced blood supply to breast tissue.
  • Clinical diagnosis of depression or other mental health disorders, including body dysmorphic disorder and eating disorders. Please discuss any history of mental health disorders with your surgeon prior to surgery. Patients with a diagnosis of depression or other mental health disorders should wait for resolution or stabilization of these conditions prior to undergoing breast implantation surgery.

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.htm.

Natrelle® Breast Implants are available by prescription only.

Most of the SkinMedica® products described here 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 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

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.

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

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.

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 Product 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.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.FDA.gov/safety/MedWatch or call 1-800-FDA-1088.

Please talk to your healthcare provider or see full Prescribing 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 injectable gel is 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 injection into the facial tissue for the correction of moderate to severe facial wrinkles and folds, such as nasolabial folds in adults over 21.

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

JUVÉDERM VOLBELLA® XC injectable gel is for injection into the lips for lip augmentation and for correction of perioral lines in adults over the age of 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?
  • Tell your doctor if you are pregnant or breastfeeding. The safety of these products for use during pregnancy or while breastfeeding has not been studied
  • The safety of JUVÉDERM VOLUMA® XC in patients under 35 years or over 65 years, the safety of JUVÉDERM® XC and JUVÉDERM® Ultra XC injectable gels in patients under 18 years, and the safety of JUVÉDERM VOLLURE™ XC and JUVÉDERM VOLBELLA® XC in patients under 22 years has not been studied
  • The safety and effectiveness of JUVÉDERM VOLUMA® XC in areas other than the cheek area, JUVÉDERM® XC and JUVÉDERM VOLLURE™ XC for areas other than facial wrinkles and folds, and JUVÉDERM® Ultra XC and JUVÉDERM VOLBELLA®XC in areas other than the lips and perioral area have not been established in clinical studies
  • Tell your doctor if you have a history of excessive scarring (eg, hypertrophic scarring and keloid formations) or pigmentation disorders, as use of these products may result in additional scars or changes in pigmentation
  • Tell your doctor if you are planning other laser treatments or a chemical peel, as there is a possible risk of inflammation at the treatment site if these procedures are performed after treatment
  • Patients who experience skin injury near the site of injection with this product may be at higher risk for side effects
  • Tell your doctor if you are on immunosuppressive therapy used to decrease the body’s immune response, as use of these products may result in an increased risk of infection
  • Tell your doctor if you are using medications that can prolong bleeding, such as aspirin, ibuprofen, or other blood thinners, as this may result in increased bruising or bleeding at the injection site
  • Minimize strenuous exercise, exposure to extensive sun or heat, and alcoholic beverages within the first 24 hours following treatment

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 for women at least 22 years old for silicone-filled implants.
  • Breast augmentation for women at least 18 years old for saline-filled implants.

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?
  • Women with active infection anywhere in their body.
  • Women with existing cancer or precancer of their breast who have not received adequate treatment for those conditions.
  • Women who are currently pregnant or nursing.
What should I know before getting breast implants?
  • Breast implants are not lifetime devices, and not necessarily a one-time surgery.
  • Many of the changes to your breasts following implantation cannot be undone. If you later choose to have your implant(s) removed and not replaced, you may experience unacceptable dimpling, puckering, wrinkling, or other cosmetic changes of the breast, which may be permanent.
  • Breast implants may affect your ability to breast-feed, either by reducing or eliminating milk production.
  • Rupture of a silicone-filled breast implant is most often silent and may not be detected by you or your doctor. You should have an MRI 3 years after your surgery and then every 2 years after that for as long as you have your breast implants to determine if rupture is present. If implant rupture is noted on an MRI, you should have the implant removed, with or without replacement.
  • With breast implants, a routine screening mammography and self-examinations for breast cancer will be more difficult. Ask your doctor to help you distinguish the implant from your breast tissue. Symptoms of a ruptured implant may be hard knots or lumps surrounding the implant or in the armpit, change or loss of size or shape of the breast or implant, pain, tingling, swelling, numbness, burning, or hardening. Tell your doctor of these symptoms and remove ruptured implants.
  • Inform any other doctor who treats you of the presence of your implants to minimize the risk of damage to the 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:
  • Autoimmune diseases (for example, lupus and scleroderma).
  • A weakened immune system (for example, currently taking drugs that weaken the body’s natural resistance to disease).
  • Planned chemotherapy following breast implant placement.
  • Planned radiation therapy to the breast following breast implant placement.
  • Conditions or medications that interfere with wound healing and blood clotting.
  • Reduced blood supply to breast tissue.
  • Clinical diagnosis of depression or other mental health disorders, including body dysmorphic disorder and eating disorders. Please discuss any history of mental health disorders with your surgeon prior to surgery. Patients with a diagnosis of depression or other mental health disorders should wait for resolution or stabilization of these conditions prior to undergoing breast implantation surgery.

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.htm.

Natrelle® Breast Implants are available by prescription only.

Most of the SkinMedica® products described here 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 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.