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PRT143930 02/21

Earning double Allē points is as simple as making one appointment to get treated with both! Earn up to $180 in points and redeem them on a variety of Allergan Aesthetics treatments. Make sure you’re an Allē Member to take advantage of this limited-time opportunity. 

LEARN HOW TO EARN

Consult a specialist about getting treated with both a JUVÉDERM® product and BOTOX® Cosmetic. Make sure you’re an Allē Member before treatment to earn double points. If you're not a member, sign up now!

Get treated with BOTOX® Cosmetic and any product from the JUVÉDERM® Collection of Fillers during the same appointment between February 9 and May 9 by a participating Allē provider. Only your doctor or specialist can determine if BOTOX® Cosmetic and JUVÉDERM® are right for you.


YOUR ALLE POINTS CAN BE USED TO:

Smooth

Fill

Sculpt

WITH JUVÉDERM® Collection of Fillers

WITH COOLSCULPTING®

The #1 selling product of its kind used to temporarily smooth the appearance of moderate to severe frown lines, crow's feet, and forehead lines in adults. 

The #1 chosen filler collection with products that treat different areas of the face.

Transform

WITH SKINMEDICA®

Get a personalized skin care regimen made with proven ingredients.

Glow

Get a next-level skin treatment that leaves the skin looking luminous, nourished, and renewed.

Strengthen, tone, and firm the muscles of the abdomen, buttocks, and thighs.

Improve

WITH KYBELLA® 
(deoxycholic acid) injection 10 mg/mL

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).

Grow

WITH LATISSE®
(bimatoprost ophthalmic solution) 0.03%

The first FDA-approved prescription treatment to grow lashes for people with inadequate or not enough eyelashes.

Tone

WITH COOLTONE®

WITH BOTOX® COSMETIC

 LIMITED-TIME OFFER.

@botoxcosmetic

@juvederm

BOOK A CONSULTATION

The #1 nonsurgical fat reducing treatment used by doctors.*

Enhance

WITH NATRELLE®

Get state-of-the-art gel breast implants made with gummy technology.

FOLLOW US ON INSTAGRAM TO STAY IN THE LOOP

*CoolSculpting® is the treatment doctors use most for nonsurgical fat reduction.

WITH DIAMONDGLOWTM

EARN DOUBLE POINTS ON JUVÉDERM® WHEN ADDED TO A BOTOX® COSMETIC (onabotulinumtoxinA) APPOINTMENT

The safe and effective use of these products has not been studied together.

FIND A SPECIALIST

POWERED BY

EARN DOUBLE POINTS WITH THE #1 SELLING PRODUCTS OF THEIR KIND.

GET TREATED

STEP 1

STEP 2

HOW TO EARN DOUBLE POINTS

Double Points on JUVÉDERM® Promotion
TERMS AND CONDITIONS
•  Members who purchase treatments with both BOTOX® Cosmetic (onabotulinumtoxinA) and at least one of any 
   JUVÉDERM® Collection of Fillers products in the same visit will earn double AllēSM Loyalty Program points on up to four 
   qualifying syringes of any JUVÉDERM® product (1,600 maximum JUVÉDERM® points).  

•  Members will earn standard Allē points on all other eligible purchases. 

•  A healthcare provider will determine if a member is an appropriate candidate for a JUVÉDERM® Collection of Fillers and 
   a BOTOX® Cosmetic treatment. 

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

•  BOTOX® Cosmetic and JUVÉDERM® treatments must occur in the same visit and be part of the same Allē transaction to 
   qualify for Double Points offer. 

•  Treatments must occur between February 9, 2021 and May 9, 2021 to be eligible for Double Points offer. 

•  Standard Allē Loyalty Program Terms and Conditions apply, including Earnings Caps

•  Double Points offer cannot be applied to past transactions. 

•  Please allow up to 48 hours for points to deposit into members’ Allē accounts. 

•  Double Points Offer can be combined with other Allē, BOTOX® Cosmetic and JUVÉDERM® offers, Allē, BOTOX® Cosmetic 
   and JUVÉDERM® gift cards or Allē points. 

•  If you have questions, please contact Allē Customer Support at 1-888-912-1572 Monday — Friday, 8 am — 6 pm CT.

•  Allergan Aesthetics, an AbbVie company, reserves the right to alter or cancel this offer at any time. 

EARN DOUBLE POINTS ON 
JUVÉDERM® 
WHEN ADDED 
TO A BOTOX® COSMETIC 
APPOINTMENT

Double Points on JUVÉDERM® Promotion
TERMS AND CONDITIONS
•  Members who purchase treatments with both 
   BOTOX® Cosmetic (onabotulinumtoxinA) and at least 
   one of any 
   JUVÉDERM® Collection of Fillers products in the 
   same visit will earn double AllēSM Loyalty Program 
   points on up to four qualifying syringes of any 
   JUVÉDERM® product (1,600 maximum 
   JUVÉDERM® points).  

•  Members will earn standard Allē points on all other      eligible purchases. 

•  A healthcare provider will determine if a member 
   is an appropriate candidate for a JUVÉDERM® 
   Collection of Fillers and a BOTOX® 
   Cosmetic treatment. 

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

•  BOTOX® Cosmetic and JUVÉDERM® treatments must 
   occur in the same visit and be part of the same Allē 
   transaction to qualify for Double Points offer. 

•  Treatments must occur between February 9, 2021 
    and May 9, 2021 to be eligible for Double Points 
    offer. 

•  Standard 
   Allē Loyalty Program Terms and Conditions apply, 
   including Earnings Caps

•  Double Points offer cannot be applied to past 
   transactions. 

•  Please allow up to 48 hours for points to deposit 
   into members’ Allē accounts. 

•  Double Points Offer can be combined with other 
   Allē, BOTOX® Cosmetic and JUVÉDERM® offers, Allē, 
   BOTOX® Cosmetic and JUVÉDERM® gift cards or 
   Allē points. 

•  If you have questions, please contact Allē Customer 
   Support at 1-888-912-1572 Monday — Friday, 
   8 am — 6 pm CT.

•  Offer can be combined with Allē and specific brand 
   gift cards, offers, and points excluding BOTOX® 
   Cosmetic offers.

•  Allergan Aesthetics, an AbbVie company, reserves 
   the right to alter or cancel this offer at any time. 

BOTOX® Cosmetic IMPORTANT SAFETY INFORMATION & APPROVED USES

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, and 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, and/or forehead lines.


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 receive  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; have 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 over-the-counter medicines, vitamins, and herbal supplements. 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: dry mouth; discomfort or pain at the injection site; tiredness; headache; neck pain; and eye problems: double vision, blurred vision, decreased eyesight, drooping eyelids and eyebrows, swelling of your eyelids and dry eyes.


APPROVED USES


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


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 


JUVÉDERM® Injectable Gel Fillers Important Information
APPROVED USES
JUVÉDERM® VOLUMA™ XC injectable gel for deep injection in the cheek area to correct age-related volume loss and for augmentation of the chin region to improve the chin profile in adults over 21.

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

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


IMPORTANT SAFETY INFORMATION

Are there any reasons why I should not receive any JUVÉDERM® 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?
• Minimize strenuous exercise and exposure to extensive sun or heat within the first 24 hours following treatment. Exposure to any of these may cause temporary redness, swelling, and/or itching at the injection site
• 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 has not been studied in patients under 35 years or over 65 years for cheek augmentation, or under 22 years and over 80 years for chin augmentation. The safety of JUVÉDERM® VOLLURE™XC and JUVÉDERM® VOLBELLA™ XC has not been studied in patients under 22 years, and the safety of JUVÉDERM® XC and JUVÉDERM® Ultra XC has not been studied in patients under 18 years
• JUVÉDERM® VOLUMA™ XC is intended for use in the chin and cheek areas. JUVÉDERM® VOLLURE™ XC and JUVÉDERM®® XC are intended for use in facial wrinkles and folds. JUVÉDERM® VOLBELLA™ XC and JUVÉDERM® Ultra XC are intended for use in the lips and perioral area. The safety and effectiveness for treatment in other areas have not been established in clinical studies
• Tell your doctor if you have a history of excessive scarring (thick, hard scars) or pigmentation disorders. The safety of JUVÉDERM® products has not been studied in these patients and may result in additional scars or changes in pigmentation
• Tell your doctor if you are on therapy used to decrease the body’s immune response (immunosuppressive therapy). Use may result in an increased risk of infection
• Tell your doctor before treatment if you are using substances that can prolong bleeding, such as aspirin, ibuprofen, or other blood thinners. As with anyinjection, this may result in increased bruising or bleeding at the injection site
• Patients who experience skin injury near the site of injection may be at a higher risk for adverse events
• JUVÉDERM® VOLUMA™ XC was not studied in patients with significant loose skin of the chin, neck, or jaw
• The effect of JUVÉDERM® VOLUMA™ XC injection into the chin on facial hair growth has not been studied

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 resolved withing 2 to 4 weeks. For JUVÉDERM® VOLLURE™ XC, JUVÉDERM® XC, and JUVÉDERM® Ultra XC injectable gels, most resolved within 14 days or less. For JUVÉDERM® VOLBELLA™ XC
most resolved within 30 days or less. These side effects are consistent with other facial injection procedures.

Most side effects will resolve with time. Your doctor may choose to treat side effects persisting over 30 days with antibiotics, steroids, or hyaluronidase (an enzyme that breaks down hyaluronic acid). scarring.

One of the risks with these products is unintentional injection into a blood vessel. The chances of this happening are very small, but if it does happen, 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 of the skin. 

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

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

Products in the JUVÉDERM® Collection are available only by a licensed physician or properly licensed practitioner.


COOLSCULPTING® TREATMENT IMPORTANT INFORMATION

USES
The CoolSculpting® procedure is 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. The CoolSculpting® procedure is not a treatment for weight loss.

IMPORTANT SAFETY INFORMATION
The CoolSculpting® procedure is not for everyone. You should not have the CoolSculpting® procedure 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® may cause a visible enlargement in the treated area which may develop two to five months after treatment and requires surgical intervention for correction.

Please see full Important Safety Information for additional information.


COOLTONE® TREATMENT IMPORTANT INFORMATION


USES
The CoolTone® device is FDA-cleared for improvement of abdominal tone, strengthening of the abdominal muscles, and development for firmer abdomen. CoolTone® is also FDA-cleared for strengthening, toning, and firming of buttocks and thighs.

IMPORTANT SAFETY INFORMATION
The CoolTone® procedure is not for everyone. You should not have the CoolTone® treatment in areas with metal, electrical, or electronic implants/devices like cardiac pacemakers, implanted hearing devices, implanted defibrillators, implanted neurostimulators, drug pumps, or hearing aids.

Tell your doctor if you have any medical conditions as CoolTone® should not be used over a menstruating uterus, over areas of the skin that lack normal sensation, in patients with fever, malignant tumor, hemorrhagic conditions, epilepsy, recent surgical procedure, pulmonary insufficiency, or pregnancy.

CoolTone® should be used with caution in patients with Graves’ disease (an autoimmune disorder that causes overactive thyroid), active bleeding disorders, or seizure disorders.

Women who are close to menstruation may find that it comes sooner, or cramping is increased or intensified with CoolTone® treatments, therefore, it is recommended to not undergo treatment during this time of the month.

CoolTone® should not be used in the heart or head areas, areas of new bone growth, over the carotid sinus nerves, or over the neck or mouth. CoolTone® should not be applied over swollen, infected, inflamed areas or skin eruptions. Caution should be used for patients with suspected or diagnosed heart problems.

Common side effects may include, but may not be limited to, muscular pain, temporary muscle spasm, temporary joint or tendon pain, and redness at or near the treatment site.

Ask your Healthcare Provider if CoolTone® is right for you.

Please see full Important Safety Information for additional information at coolsculpting.com/cooltone.


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+) and Essential Defense Broad Spectrum Sunscreens (Everyday Clear SPF 47, Mineral Shield Tinted SPF 32, and Mineral Shield SPF 35) 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® Purifying Foaming Wash is an over-the-counter drug product which is formulated and marketed pursuant to the FDA’s governing regulations set forth at 21 C.F.R. Part 333, Subpart D.

DIAMONDGLOW™ TREATMENT IMPORTANT INFORMATION

USES

The DiamondGlow™ device is a general dermabrasion device that gently removes the top layer of skin and delivers topical cosmetic serums onto the skin.

IMPORTANT SAFETY INFORMATION

The DiamondGlow™ treatment is not for everyone. You should not have a DiamondGlow™ treatment if you have compromised skin quality. Tell your provider if you are pregnant or lactating, or if you have any medical conditions, including allergies, and if you are using topical medication on the area to be treated.

Typical side effects include a scratchy, stinging sensation during the treatment and temporary tightness, redness or slight swelling after the treatment. Rare serious side effects may also occur and include severe skin irritation and allergic reactions.

SkinMedica® Pro-Infusion Serums Disclaimer
The SkinMedica® Pro-Infusion Serums 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 products are not intended to be drugs 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.

Please talk to your provider for additional information.


KYBELLA® (deoxycholic acid) injection 10 mg/mL IMPORTANT SAFETY INFORMATION

What is KYBELLA®?

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 the treatment of fat outside of the submental area or in children under 18 years of age.

Who should not receive KYBELLA®?
Do 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).

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)
• Trouble swallowing
• Injection site problems including: a collection of blood under the skin (hematoma) or bruising, damage to an artery or vein if KYBELLA® is inadvertently injected into it, hair loss, open sores (ulcers), damage and tissue cell-death (necrosis) around the injection site. Call your healthcare provider if you: begin to develop weakness in the muscles of your face, or your smile becomes uneven; have difficulty swallowing, or if any of the symptoms that you already have get worse; develop open sores or drainage from the treatment area

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

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

Please see KYBELLA® full Prescribing Information.

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

Do not use LATISSE® if you are allergic to one of its ingredients. 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.

These are not all the possible side effects of LATISSE®. For more information, please talk to your doctor.

Please see LATISSE® full Product Information.

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.

• Breast reconstruction. Breast reconstruction includes primary reconstruction to replace breast tissue that has been removed due to cancer or trauma or that has failed to develop properly due to a severe breast abnormality. Breast reconstruction also includes revision surgery to correct or improve the result of a primary breast reconstruction 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 breastfeed, 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 see the patient brochures at www.allergan.com/products
To report a problem with Natrelle® Breast Implants, please call Allergan at 1-800-433-8871.

Natrelle® Breast Implants are available by prescription only.

The safe and effective use of these products has not been studied together.