Frequently Asked
Questions

Coverage, Limits, and Eligibility

How to Enroll

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Who is eligible?

You are eligible if you:

  • Are currently receiving BOTOX® treatment for an FDA-approved therapeutic indication for BOTOX®
  • Are commercially insured
  • Are not enrolled in or eligible for Medicare, Medicaid, or other federal or state healthcare programs
  • Are 18 years or older (or are the parent or caregiver of a patient under the age of 18 who is receiving BOTOX® treatment)
  • Receive treatment in the United States or territories

Void where prohibited by law, taxed, or restricted. Please see full Terms and Conditions.

Coverage and Limits

About the BOTOX® Savings card

Coverage, Limits, and Eligibility

Using the Digital BOTOX® Specialty Pharmacy Card

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Does the BOTOX® Savings Program help with costs related to my BOTOX® procedure?

Yes, the BOTOX® Savings Program helps eligible patients save on out-of-pocket costs related to both BOTOX® medicine and the injection procedure. This could be a co-pay, co-insurance, or deductible amount; sometimes these charges are billed separately from one another.* The BOTOX® Savings Program does not provide help for office visit co-pay costs.

*For residents of some states, offer applies only to the cost of BOTOX® and not to any related medical service(s).

How to Submit or Check on a Claim

Using Your BSP Dashboard

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How do I file a claim?

  1. Enroll at BOTOXSavingsProgram.com or call 1-800-44-BOTOX.
  2. After completing your BOTOX® treatment and receiving your Explanation of Benefits (EOB) from your insurance, you are ready to submit your claim.
  3. Enter your treatment details on the website and upload your EOB and any other documents to show your out-of-pocket (OOP) costs and prove you were treated for an FDA-approved indication.
  4. We will confirm you received BOTOX® treatment for an FDA-approved indication and verify your OOP responsibility.
  5. Upon approval, you will be mailed a check for your OOP costs up to the allowed amount. Expect to receive your check 2-3 weeks after submitting your claim.

We will keep you updated at each step of the way by mail, email, or text message (if you opted in to receive text messages) so you know where your claim is at any time. You will be notified if we need additional information. You can also log in to BOTOXSavingsProgram.com to check the status of your claim.

Be sure to submit a claim and follow the same process after every future treatment with BOTOX®.

Coverage, Limits, and Eligibility

Using the Digital BOTOX® Specialty Pharmacy Card

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Is there a time limit for submitting my claim?

Yes. All claims must be submitted within 6 months (180 days) from the treatment date. You may ask for a one-time exception if your claim is beyond 180 days by calling 1-800-44-BOTOX. We are unable to process any claims beyond 365 days.

How to Enroll

Using the Digital BOTOX® Specialty Pharmacy Card

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What if I use a specialty pharmacy (SP)?

After enrolling at BOTOXSavingsProgram.com prior to treatment, you should receive a welcome email with your digital SP Card details. When you are due for BOTOX® treatment:

  1. Your physician will send the BOTOX® prescription to the SP to be filled.
  2. When your SP calls you to collect your out-of-pocket (OOP) responsibility (co-pay/co-insurance), simply provide the BIN, PCN, GRP#, and ID# from your digital SP Card to the SP. The SP applies the eligible benefit from the digital SP Card toward your OOP.
  3. After treatment, you may still submit an Explanation of Benefits (EOB) for reimbursement of procedure expenses* at BOTOXSavingsProgram.com. For each additional treatment, repeat step 2 above.

*For residents of some states, offer applies only to the cost of BOTOX® and not to any related medical service(s).

How to Submit or Check on a Claim

Using the Digital BOTOX® Specialty Pharmacy Card

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What is an EOB?

An EOB, or Explanation of Benefits, is a statement from your health insurance plan describing what costs it will cover for your BOTOX® treatment and if you have any out-of-pocket costs. Other terms for an EOB may include Summary of Benefits, Claim Details, or Coverage Determination. After your BOTOX® treatment, you will receive an EOB either by mail or email from your insurance provider.

Using Your BSP Dashboard

Using the Digital BOTOX® Specialty Pharmacy Card

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Will my EOB be the only document I need to submit?

Sometimes, submitting an Explanation of Benefits (EOB) will meet the documentation requirements. Occasionally, an EOB will not include the information needed for us to verify that you received BOTOX® treatment for an FDA-approved indication. In this situation, we may require you to submit additional documentation, such as an itemized receipt or bill from your doctor showing your out-of-pocket expense for the BOTOX® medicine and procedure.

How to Submit or Check on a Claim

Using the Digital BOTOX® Specialty Pharmacy Card

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When will I receive my BOTOX® Savings Program check?

Upon approval, expect your check to arrive in the mail within 2-3 weeks from claim submission. If you do not receive your check by then, or if you lose your check, please call 1-800-44-BOTOX to speak to a representative.

How to Enroll

Using the Digital BOTOX® Specialty Pharmacy Card

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How do I enroll in the BOTOX® Savings Program?

There are 3 easy ways to enroll:

How to Enroll

Using the Digital BOTOX® Specialty Pharmacy Card

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Where can I find my username and password?

Your username is the email address that you used to register for the program. If you have forgotten your password:

  1. Click “Log In” at the top right portion of the BOTOXSavingsProgram.com screen.
  2. Scroll down to click “Forgot Password”.
  3. You’ll receive a temporary password at the email address that you used to register for the program. Be sure to check your spam folder if you don't see the temporary password email in your in-box.

Please call 1-800-44-BOTOX if this does not resolve the issue. 

How to Enroll

Using the Digital BOTOX® Specialty Pharmacy Card

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What do AbbVie and its authorized partners do with my information?

AbbVie and its authorized partners use the information you provide for legitimate business purposes only and will not sell, share, or otherwise distribute your personal information to third parties. Please see BOTOX® Savings Program Terms and Conditions, Privacy Notice, and Mobile Terms and Conditions for more information.

How to Enroll

Using the Digital BOTOX® Specialty Pharmacy Card

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What if I still have questions about the BOTOX® Savings Program?

You can speak with a representative Monday through Friday, from 8 AM to 8 PM ET by simply calling 1-800-44-BOTOX.

How to Enroll

Using the Digital BOTOX® Specialty Pharmacy Card

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Where can I go for more information about my condition?

Select your condition:

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INDICATIONS

BOTOX® (onabotulinumtoxinA) is a prescription medicine that is injected into muscles and used:

IMPORTANT SAFETY INFORMATION

BOTOX 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 :


IMPORTANT SAFETY INFORMATION

BOTOX 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:

  • 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 preexisting 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; drooping eyelids; hoarseness or change or loss of voice; trouble saying words clearly; loss of bladder control; trouble breathing; and trouble swallowing.

INDICATIONS

BOTOX® (onabotulinumtoxinA) is a prescription medicine that is injected into muscles and used:

  • To treat overactive bladder symptoms such as a strong need to urinate with leaking or wetting accidents (urge urinary incontinence), a strong need to urinate right away (urgency), and urinating often (frequency) in adults 18 years and older when another type of medicine (anticholinergic) does not work well enough or cannot be taken
  • To treat leakage of urine (incontinence) in adults 18 years and older with overactive bladder due to a neurologic disease when another type of medicine (anticholinergic) does not work well enough or cannot be taken
  • To treat overactive bladder due to a neurologic disease in children 5 years of age and older when another type of medicine (anticholinergic) does not work well enough or cannot be taken
  • To prevent headaches in adults with chronic migraine who have 15 or more days each month with headache lasting 4 or more hours each day in people 18 years and older
  • To treat increased muscle stiffness in people 2 years of age and older with spasticity
  • To treat the abnormal head position and neck pain that happens with cervical dystonia (CD) in people 16 years and older
  • To treat certain types of eye muscle problems (strabismus) or abnormal spasm of the eyelids (blepharospasm) in people 12 years of age and older

BOTOX is also injected into the skin to treat the symptoms of severe underarm sweating (severe primary axillary hyperhidrosis) when medicines used on the skin (topical) do not work well enough in people 18 years and older.

It is not known whether BOTOX is safe and effective to prevent headaches in patients with migraine who have 14 or fewer headache days each month (episodic migraine).

BOTOX has not been shown to help people perform task-specific functions with their upper limbs or increase movement in joints that are permanently fixed in position by stiff muscles.

It is not known whether BOTOX is safe and effective for severe sweating anywhere other than your armpits.

IMPORTANT SAFETY INFORMATION (continued)

There has not been a confirmed serious case of spread of toxin effect away from the injection site when BOTOX has been used at the recommended dose to treat chronic migraine, severe underarm sweating, blepharospasm, or strabismus.

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

Do not receive BOTOX if you are allergic to any of the ingredients in BOTOX (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.

Do not receive BOTOX for the treatment of urinary incontinence if you have a urinary tract infection (UTI) or cannot empty your bladder on your own and are not routinely catheterizing. Due to the risk of urinary retention (difficulty fully emptying the bladder), only patients who are willing and able to initiate catheterization posttreatment, if required, should be considered for treatment.

Patients treated for overactive bladder: In clinical trials, 36 of the 552 patients had to self-catheterize for urinary retention following treatment with BOTOX compared to 2 of the 542 treated with placebo. The median duration of postinjection catheterization for these patients treated with BOTOX 100 Units (n = 36) was 63 days (minimum 1 day to maximum 214 days), as compared to a median duration of 11 days (minimum 3 days to maximum 18 days) for patients receiving placebo (n = 2). Patients with diabetes mellitus treated with BOTOX were more likely to develop urinary retention than nondiabetics.

Adult patients treated for overactive bladder due to a neurologic disease: In clinical trials, 30.6% of adult patients (33/108) who were not using clean intermittent catheterization (CIC) prior to injection required catheterization for urinary retention following treatment with BOTOX 200 Units, as compared to 6.7% of patients (7/104) treated with placebo. The median duration of postinjection catheterization for these patients treated with BOTOX 200 Units (n = 33) was 289 days (minimum 1 day to maximum 530 days), as compared to a median duration of 358 days (minimum 2 days to maximum 379 days) for patients receiving placebo (n = 7).

Among adult patients not using CIC at baseline, those with multiple sclerosis were more likely to require CIC postinjection than those with spinal cord injury.

The dose of BOTOX is not the same as, or comparable to, another botulinum toxin product.

Serious and/or immediate allergic reactions have been reported, including itching; rash; red, itchy welts; wheezing; asthma symptoms; dizziness; or feeling faint. Get medical help right away if you experience symptoms; further injection of BOTOX should be discontinued.

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.

Tell your doctor if you have any breathing-related problems. Your doctor may monitor you for breathing problems during treatment with BOTOX for spasticity or for detrusor overactivity associated with a neurologic condition. The risk of developing lung disease in patients with reduced lung function is increased in patients receiving BOTOX.

Cornea problems have been reported. Cornea (surface of the eye) problems have been reported in some people receiving BOTOX for their blepharospasm, especially in people with certain nerve disorders. BOTOX may cause the eyelids to blink less, which could lead to the surface of the eye being exposed to air more than is usual. Tell your doctor if you experience any problems with your eyes while receiving BOTOX. Your doctor may treat your eyes with drops, ointments, contact lenses, or with an eye patch.

Bleeding behind the eye has been reported. Bleeding behind the eyeball has been reported in some people receiving BOTOX for their strabismus. Tell your doctor if you notice any new visual problems while receiving BOTOX.

Bronchitis and upper respiratory tract infections (common colds) have been reported. Bronchitis was reported more frequently in adults receiving BOTOX for upper limb spasticity. Upper respiratory infections were also reported more frequently in adults with prior breathing-related problems with spasticity. In pediatric patients treated with BOTOX for upper limb spasticity, upper respiratory tract infections were reported more frequently. In pediatric patients treated with BOTOX for lower limb spasticity, upper respiratory tract infections were not reported more frequently than placebo.

Autonomic dysreflexia in patients treated for overactive bladder due to a neurologic disease. Autonomic dysreflexia associated with intradetrusor injections of BOTOX could occur in patients treated for detrusor overactivity associated with a neurologic condition and may require prompt medical therapy. In clinical trials, the incidence of autonomic dysreflexia was greater in adult patients treated with BOTOX 200 Units compared with placebo (1.5% versus 0.4%, respectively).

Tell your doctor about all your medical conditions, including if you have or have had bleeding problems; have plans to have surgery; had surgery on your face; have weakness of forehead muscles, trouble raising your eyebrows, drooping eyelids, and any other abnormal facial change; have symptoms of a UTI and are being treated for urinary incontinence (symptoms of a UTI may include pain or burning with urination, frequent urination, or fever); have problems emptying your bladder on your own and are being treated for urinary incontinence; are pregnant or plan to become pregnant (it is not known if BOTOX can harm your unborn baby); are breastfeeding or plan to (it is not known if BOTOX 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 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 in the past.

Tell your doctor if you 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 include dry mouth; discomfort or pain at the injection site; tiredness; headache; neck pain; eye problems such as double vision, blurred vision, decreased eyesight, drooping eyelids, swelling of your eyelids, and dry eyes; drooping eyebrows; and upper respiratory tract infection. In adults being treated for urinary incontinence, other side effects include UTI and painful urination. In children being treated for urinary incontinence, other side effects include UTI and bacteria in the urine. In patients being treated for urinary incontinence, another side effect includes the inability to empty your bladder on your own. If you have difficulty fully emptying your bladder on your own after receiving BOTOX, you may need to use disposable self-catheters to empty your bladder up to a few times each day until your bladder is able to start emptying again.

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

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

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

If you are having difficulty paying for your medicine, AbbVie may be able to help. Visit AbbVie.com/myAbbVieAssist to learn more.

For questions about the program, please call 1-800-44-BOTOX .