Prepare for your
consultation
Heidi, age 43, mom of 2
Actual patient.
Individual results may vary.

This interactive tool is designed to help you learn about available surgeries and treatments. You can create a list of treatment options to bring to your surgeon for discussion during your consultation. This will help you get the most out of your appointment.

To use the interactive tool, simply choose the surgery or treatment options of interest. When you’re finished, you will have created your own list of treatment options, along with helpful questions to ask your surgeon.

Let’s get started!

Breast implants before and after

Natrelle INSPIRA® Style SRF-415
Individual results may vary.

BREAST

Learn about Natrelle® Gel breast implants for breast augmentation


BREAST AUGMENTATION

If you've never had breast implants, Natrelle® offers you and your surgeon the most breast implant options to help you find the full look you want.

BREAST REVISION

If you’ve already had breast implants and would like to change your look, Natrelle® offers you a full range of breast implant options that are right for you. Have saline breast implants? Talk to your doctor about switching to Natrelle® cohesive silicone-filled gel implants. You’ll experience rewards and savings you won’t find anywhere else.

NO THANKS
YES
Body before and after

Individual results may vary.

BODY

FIRM AND FLATTEN WITHOUT SURGERY

While many moms opt for a tummy tuck to address loose skin after pregnancy, there are nonsurgical body contouring options as well.

Talk to your surgeon about your specific concerns and which treatments are right for you.

NONSURGICAL BODY CONTOURING

NO THANKS
YES
PREVIOUS
Tummy before and after

Individual results may vary.

TUMMY TUCK

With a tummy tuck, your doctor will remove extra fat and skin to create a smoother, firmer, and flatter look in your tummy area.

NO THANKS
YES
PREVIOUS
SKINMEDICA(R) scar Recovery Gel with Centelline(R) before and after

Individual results may vary. Data on file at SkinMedica®.

SCARS

Learn about improving the appearance of scars

Scar Recovery Gel with Centelline®

Help minimize the appearance of new scars with this first-of-its-kind, proprietary gel formulation with Centelline®.

  • Works to smooth and minimize the appearance of existing scars
  • Diminishes the look of scars from cosmetic, general, and reconstruction surgeries, as well as C-sections and everyday cuts

Diminish the appearance of red or pink scars

NO THANKS
YES
PREVIOUS

Actual patient. Results may vary. Prescription only.

Photos taken at maximum frown before and after treatment with BOTOX® Cosmetic at day 7. In clinical studies, physicians assessed 80% of people had significant improvement at day 30.

Side effects associated with the injection include localized pain, infection, inflammation, tenderness, swelling, redness, and/or bleeding/bruising.

FROWN LINES

Learn about temporarily improving moderate to severe frown lines between your brows

BOTOX® Cosmetic targets one of the underlying causes of frown lines—the repeated muscle contractions from frowning over the years. Your provider will inject these muscles with
BOTOX® Cosmetic to temporarily reduce muscle activity. You will begin to notice a visible smoothing of your frown lines between your brows.

Tell your doctor about all your medical conditions, including if you are breast-feeding or plan to (it is not known if BOTOX® Cosmetic passes into breast milk).

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

Please click here for BOTOX® Cosmetic Indications and Important Safety Information, including Boxed Warning and Medication Guide.

Soften Frown lines

NO THANKS
YES
PREVIOUS
Before and after pictures of moderate to severe crow’s feet treated with Botox Cosmetic (onabotulinumtoxinA)

Actual patient. Results may vary. Prescription only.

Photos taken at full smile before and after treatment with BOTOX® Cosmetic at day 7. In two clinical studies, 26.1% and 20.3% of people had ≥ 2-grade improvement at day 30. In one of these studies, 67.9% of people had mild or no crow’s feet at day 30 after treatment.

Side effects associated with the injection include localized pain, infection, inflammation, tenderness, swelling, redness, and/or bleeding/bruising.

CROW'S FEET

Learn about temporarily improving moderate to severe crow’s feet lines

BOTOX® Cosmetic targets one of the underlying causes of crow’s feet—the repeated muscle contractions from squinting over the years. Your provider will inject these muscles with
BOTOX® Cosmetic to temporarily reduce muscle activity. You will begin to notice a visible smoothing of your crow’s feet lines.

Tell your doctor about all your medical conditions, including if you are breast-feeding or plan to (it is not known if BOTOX® Cosmetic passes into breast milk).

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

Please click here for BOTOX® Cosmetic Indications and Important Safety Information, including Boxed Warning and Medication Guide.

Less noticeable crow’s feet lines

NO THANKS
YES
PREVIOUS

Actual patient. Results may vary. Prescription only.
Unretouched photos taken before treatment and 1 month after treatment. A total of 3.5 mL of JUVÉDERM VOLUMA® XC was injected into the cheek area. The average volume of JUVÉDERM VOLUMA® XC injected during the clinical study was 6.8 mL to achieve optimal correction for the cheek area.

CHEEKS

Learn about correcting age-related volume loss in the cheeks

As we age, our 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 is designed to add just enough volume to subtly and instantly lift and contour the cheek area, and is also the only filler proven to last up to 2 years in the cheek area with optimal treatment.

Lift and contour cheeks

NO THANKS
YES
PREVIOUS

Actual patient. Results may vary. Prescription only.
Unretouched photos taken before treatment and 2 weeks after treatment. A total of 3.2 mL of JUVÉDERM® XC was injected into the parentheses, corner, and marionette lines. These photos are not of a clinical trial subject. The average amount of JUVÉDERM® XC injected was 1.6 mL per treatment to achieve optimal correction.

LINES & WRINKLES

Learn about smoothing moderate to severe parentheses lines and wrinkles to create a smoother appearance

JUVÉDERM® XC is a nonsurgical filler your doctor uses to instantly smooth out the lines along the sides of your nose and mouth. It can provide natural-looking results for up to 1 year with optimal treatment.

Smooth parentheses lines & wrinkles

NO THANKS
YES
PREVIOUS

Actual patient. Results may vary. Prescription only.
Unretouched photos taken before treatment and 1 month after treatment. A total of 1.2 mL of JUVÉDERM® Ultra XC was injected into the lips.

LIPS

Learn about adding fullness to lips

Whether you’ve noticed your lips thinning over time or simply want fuller lips, JUVÉDERM® Ultra XC can give you the natural-looking, long-lasting results you desire. JUVÉDERM® Ultra XC is the only filler proven to last up to 1 year in the lips with optimal treatment.

Plump and fill lips

NO THANKS
YES
PREVIOUS
Before and after pictures of patient treated with Kybella injection

Unretouched photos of paid model.
Sex: F   Age: 35   
Weight (before/after): 142.5 lbs/145.5 lbs
Individual results may vary.


Unretouched photos of paid model.
Sex: F   Age: 48   
Weight (before/after): 132.5 lbs/135 lbs
Individual results may vary.

DOUBLE CHIN

Learn about reducing the fullness beneath the chin*

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.

HELP IMPROVE YOUR CHIN PROFILE

NO THANKS
YES
PREVIOUS

FEMALE, AGE 35
Treatment: 12 weeks of twice-daily application of LYTERA® Skin Brightening Complex.
Unretouched photographs taken with cross-polarized lighting.
Individual results may vary. Data on file at SkinMedica®.

SKIN QUALITY

Learn about improving the appearance of skin tone and texture

Improve the appearance of fine lines and wrinkles, smooth and brighten skin, and enhance skin texture, tone, and resiliency with SkinMedica® products.

Brighten skin, even skin tone, and reduce the appearance of dark spots—without hydroquinone—with LYTERA® Skin Brightening Complex.

CAUTION: Do not use LYTERA® if you are pregnant, lactating, or planning to become pregnant.

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

Improve the appearance of skin tone and texture

NO THANKS
YES
PREVIOUS

Retinol Complex 0.5

FEMALE, AGE 54
Unretouched photos. Individual results may vary. Data on file at SkinMedica®.


Retinol Complex 1.0

FEMALE, AGE 59
Unretouched photos. Individual results may vary. Data on file at SkinMedica®.

LEARN ABOUT ENHANCING SKIN TONE, TEXTURE, AND RESILIENCY

Improve the appearance of overall sun damage, enhance skin tone and texture, and diminish the appearance of fine lines and coarse wrinkles.

This exclusive retinol formula is encapsulated with PhytoShield™ Complex—a proprietary, advanced antioxidant complex that maximizes retinol delivery and minimizes irritation typically associated with retinoids.

CAUTION: Do not use Retinol Complex if you are pregnant, lactating, or planning to become pregnant.

ENHANCE SKIN TONE, TEXTURE, AND RESILIENCY

NO THANKS
YES
PREVIOUS
SkinMedica(R) ILLUMINIZE PEEL(R)

LEARN ABOUT BRIGHTENING THE OVERALL APPEARANCE OF SKIN WITH MINIMAL DOWNTIME

Often referred to as The Red Carpet or Lunchtime Peel, this in-office treatment requires little to no downtime, and is appropriate for mild skin imperfections.

Peels are an in-office procedure. Ask your healthcare professional if this is right for you.

FOR PROFESSIONAL USE ONLY.
Peels must be administered by a licensed medical professional (a physician, aesthetician, or a nurse under a physicians supervision). Please contact your physician.

CAUTION: Do not use Illuminize Peel® if you are pregnant, lactating, or planning to become pregnant.

LYTERA® and Retinol Complex should be discontinued 2 to 3 days before the peel and can be resumed once the peeling process is complete.

BRIGHTEN OVERALL APPEARANCE OF SKIN

NO THANKS
YES
PREVIOUS

Unretouched photos of a paid LATISSE® model at weeks 0 and 16.
Individual results may vary.

Common side effects include itchy and red eyes.

Please see additional Important Safety Information about LATISSE®.

EYELASHES

Learn about longer, fuller, darker eyelashes

For people with inadequate or not enough lashes, LATISSE® grows lashes fuller and longer in 16 weeks so you—and your mascara—have more to work with. Whether you have always wanted longer fuller lashes or if your lashes have changed over time, LATISSE® may be able to help you get the lashes you are looking for.

Longer, fuller, darker eyelashes

NO THANKS
YES
PREVIOUS
Save with Brilliant Distinctions®
Join the Brilliant Distinctions® Rewards Program to earn and redeem points on Allergan aesthetic products.
Promotional financing with the CareCredit® credit card*
Finance your treatments with payments that fit your budget.*
*Subject to credit approval. Minimum monthly payment required. See CareCredit.com for details.
Get more with the Natrelle® Gel Rewards program
Natrelle Gel Rewards logo
Receive a complimentary BOTOX® Cosmetic (onabotulinumtoxinA) or LATISSE® (bimatoprost ophthalmic solution) 0.03% treatment* for you and a friend when you and your surgeon choose Natrelle® Gel breast implants for breast augmentation. Only a doctor can determine if BOTOX® Cosmetic or LATISSE® is right for you.
*Terms and conditions apply; for qualified patients only. Patient has the ability to choose any physician of her choice.
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Natrelle®, Natrelle INSPIRA®, and Natrelle® 410 Shaped Silicone-Filled Breast Implants Important Information

Who may get breast implants?

Approved for women for the following:

  • Breast augmentation for women at least 22 years old for silicone-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 pre-cancer of their breast who have not received adequate treatment for those conditions.
  • Women who are currently pregnant or nursing.

What else 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 risks 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, 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®, Natrelle INSPIRA®, and Natrelle® 410 Breast Implants, please call Allergan at 1-800-433-8871. Please see all the patient brochures at www.allergan.com/labeling/usa.htm.

Natrelle®, Natrelle INSPIRA®, and Natrelle® 410 Breast Implants are available by prescription only.

BOTOX® Cosmetic (onabotulinumtoxinA) Important Information

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.

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 1-800-433-8871.

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

JUVÉDERM VOLUMA® XC, JUVÉDERM® XC, and JUVÉDERM® Ultra XC 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® 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® 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® XC and JUVÉDERM® Ultra XC injectable gels in patients under 18 years, and the safety of JUVÉDERM VOLUMA® XC in patients under 35 years or over 65 years has not been studied
  • The safety and effectiveness of JUVÉDERM® XC for areas other than facial wrinkles and folds, and JUVÉDERM® Ultra XC for areas other than the lips and perioral area for lip augmentation, or facial wrinkles and folds, have not been established in clinical studies
  • The safety and effectiveness of JUVÉDERM VOLUMA® XC in areas other than the cheek 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 these products may be at a 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 common side effects include tenderness, swelling, firmness, lumps/bumps, bruising, pain, redness, discoloration, and itching. With JUVÉDERM® XC and JUVÉDERM® Ultra XC injectable gels, most side effects are mild or moderate and last 14 days or less. For JUVÉDERM VOLUMA® XC, side effects are moderate (uncomfortable) and last 2 to 4 weeks.

One of the risks with using this product 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 JUVÉDERM® XC, JUVÉDERM® Ultra XC, or JUVÉDERM VOLUMA® XC, please call Allergan Product Surveillance at 1-800-624-4261.

For more information, please see Juvederm.com or call Allergan Medical Information at 1-800-433-8871.

Available by prescription only.

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

Approved Use

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 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 talk to your healthcare provider or click here for 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

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 1-800-433-8871.

Please see the full LATISSE® Product Information.

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

Most of the SkinMedica® products described here are intended to meet the FDAs 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+) are over-the-counter drug products that are formulated and marketed pursuant to the FDA's governing regulations set forth at 21 CFR § 352.

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