BOTOX® is a prescription medicine that is injected 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 or 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®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®: 

JUVÉDERM® Injectable Gel Fillers Important Information


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

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

JUVÉDERM® VOLBELLA® XC injectable gel is for injection into the lips for lip augmentation and correction of perioral lines, and for injection into the undereye hollows to improve the appearance of undereye hollows in adults over the age of 21. 


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), if you are allergic to lidocaine or the Gram-positive bacterial proteins used in these products, or if you have had previous allergic reactions to hyaluronic acid fillers. 



Xeomin® (incobotulinumtoxinA) is a prescription medication injected into muscles and used to temporarily improve the appearance of moderate to severe frown lines between the eyebrows (glabellar lines) in adults. Xeomin® contains botulinum toxin type A, a protein purified from the bacterium Clostridium botulinum. 

Do not use XEOMIN® if you are allergic to XEOMIN® or any of the ingredients in XEOMIN® (see the end of this Guide for a list of ingredients in XEOMIN®, had an allergic reaction to any other botulinum toxin products such as rimabotulinumtoxinB (MYOBLOC®), onabotulinumtoxinA (BOTOX®, BOTOX® COSMETIC), or abobotulinumtoxinA (DYSPORT®) or have a skin infection at the planned injection site. 


Revanesse Versa+Lidocaine 

Revanesse Versa is an excellent noninvasive treatment choice for almost anyone looking to smooth lines or treat age-related facial volume loss. This FDA- approved filler is available for any patient: 

  • Over the age of 22 
  • In generally good health 
  • That fully understands the procedure 

Your provider will discuss everything with you in depth during your consultation, but generally, we do not recommend Revanesse fillers for anyone pregnant or breastfeeding or with: 

  • Visible scars at the treatment site 
  • A history of allergic reactions 
  • Acne or other inflammatory diseases of the skin like: 
  • Rosacea 
  • Psoriasis 
  • Dermatitis 

Revanesse is made up of Hyaluronic Acid, (HA) – an ingredient which is found naturally in your body as a carbohydrate and is an exceptionally homogenous filler that is enhanced by advanced technology and proprietary formula. 

If you are under the age of 22 you should not be treated with Revanesse Versa. Warning: One of the risks with using this product 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. 



. SCULPTRA® Aesthetic (injectable poly-L-lactic acid) The SCULPTRA Aesthetic implant package (i.e., lyophilized vials) is provided sterile. Caution: Federal (USA) law restricts this device to sale by or on the order of a licensed physician or properly licensed practitioner. Information for the use of SCULPTRA Aesthetic is provided in this Labeling for Physicians and the Instructions for Use, as well as in Labeling for Patients. BEFORE USING SCULPTRA Aesthetic PLEASE READ THE FOLLOWING INFORMATION THOROUGHLY. Please direct any questions to Galderma Laboratories, L.P. Fort Worth, TX 76177 USA 1-855- 425-8722 DEVICE DESCRIPTION SCULPTRA Aesthetic is an injectable implant containing microparticles of poly-L-lactic acid (PLLA), carboxymethylcellulose (USP), non-pyrogenic mannitol (USP) and sterile water for injection (USP). SCULPTRA Aesthetic is available in 367.5 mg dose vials and is to be reconstituted prior to use by the addition of 5 mL of Sterile Water for Injection, USP (SWFI) to form a sterile non-pyrogenic suspension. INTENDED USE / INDICATIONS SCULPTRA Aesthetic is indicated for use in immune-competent people as a single regimen for correction of shallow to deep nasolabial fold contour deficiencies and other facial wrinkles in which deep dermal grid pattern (cross-hatch) injection technique is appropriate. (This corresponds to Wrinkle Assessment Scores (WAS) of 2 to 4 in Figure 2 and the cross-hatch injection technique presented in Figures 3-7 in the Instructions for Use Section). CONTRAINDICATIONS SCULPTRA Aesthetic should not be used in any person who has hypersensitivity to any of the components of SCULPTRA Aesthetic (see DEVICE DESCRIPTION). SCULPTRA Aesthetic should not be used in patients with known history of or susceptibility to keloid formation or hypertrophic scarring. 2 (31) WARNINGS • SCULPTRA Aesthetic has unique injection requirements, which include injection with tunneling technique in a grid pattern that is medial to the nasolabial fold contour defect that is to be corrected (see Figures 3-7 in the INSTRUCTIONS FOR USE). The safety of other methods of injection has not been evaluated in clinical studies. 


What are RADIESSE® and RADIESSE® (+)? 

RADIESSE® and RADIESSE® (+) are dermal fillers that are used for smoothing moderate to severe facial wrinkles and folds, such as nasolabial folds (the creases that extend from the corner of your nose to the corner of your mouth). RADIESSE® is also used for correcting volume loss in the back of the hands. 


Who should not use RADIESSE® or RADIESSE® (+)? 

You should not use RADIESSE® or RADIESSE® (+) if you have an allergy to any component of the product, if you have a history of severe allergies, if you have a bleeding disorder, or if you are pregnant or breastfeeding. You should not use RADIESSE® (+) if you have an allergy to lidocaine or medicines like it. 

What is the most important information I should know about RADIESSE® and RADIESSE® (+)? 

One of the risks with using 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. If you have changes in your vision, signs of a stroke (including sudden difficulty speaking, numbness or weakness in your face, arms, or legs, difficulty walking, face drooping, severe headache, dizziness, or confusion), white appearance of the skin, or unusual pain during or shortly after treatment, you should notify your health care practitioner immediately. 

As with all procedures that involve an injection through the skin, there is a risk of infection. 

Do not use RADIESSE® or RADIESSE® (+) if you have a skin infection until it has healed. 

It is not known if RADIESSE® or RADIESSE® (+) is safe or effective in the lips, or in the area around the eyes. 

The microspheres in RADIESSE® and RADIESSE® (+) can be seen in X-rays and CT Scans. It is very important that you tell your health care provider that you have had RADIESSE® or RADIESSE® (+) dermal filler. 

If you have a history of herpes, you may experience a herpes breakout after receiving RADIESSE® or RADIESSE® (+). 

Injection in the back of the hand may result in temporary difficulty performing activities. RADIESSE® may cause nodules, bumps or lumps in the back of the hand and can last up to 1 year. 

You should minimize strenuous activity and avoid extensive sun or heat exposure for about 24 hours after treatment and until any swelling or redness has resolved. 

What should I tell my doctor before using RADIESSE® or RADIESSE® (+)? 

Tell your health care provider if you are taking blood thinners or medicines that can interfere with the clotting of blood, such as aspirin or warfarin. These medicines might make it more likely that you will experience bruising or bleeding at the injection site. Tell your health care provider if you have any diseases, injuries or disabilities of the hand, if you have a history forming large, raised scars or if you have had any other skin treatments such as skin peels. 

What are the most common adverse events with RADIESSE® or RADIESSE® (+)? 

The most common adverse events seen in clinical studies of RADIESSE® used in the hands include bruising, redness, swelling, pain, itching, nodules or bumps/lumps, difficulty performing activities, loss of sensation and other local side effects. The most common adverse events seen in clinical studies of RADIESSE® or RADIESSE® (+) used in the face include bruising, redness, swelling, pain, itching and other local side effects. 

These are not all of the possible side effects with RADIESSE® or RADIESSE® (+). Merz collects information about adverse events seen with RADIESSE® and RADIESSE® (+) outside of clinical studies. These events are included in the RADIESSE® and RADIESSE® (+) Patient Information Guide based on an assessment of seriousness and potential causal relationship to RADIESSE® or RADIESSE® (+). Please see the Patient Information Guide available at for list of these events. Tell your health care provider about any side effects that bother you or do not go away. 

Important: For full safety information, please visit or call MyMerz Solutions at 1-844-469-6379 

RADIESSE® and RADIESSE® (+) are available by prescription only. 


Botox is a drug made from a protein that works on facial muscles and causes them to relax. It can be injected into specific areas of the face in order to smooth wrinkles and lines. It can also be used to treat conditions such as excessive sweating.

When Botox is injected into a muscle, it decreases the signals that allow that muscle to tighten. The muscle can no longer contract as tightly, making skin appear smoother and preventing the lines from worsening.

The injections only take a few minutes and can be performed in one visit.

Side effects are very rare with Botox. Possible side effects include mild itching or rash, stiffness, pain, temporary muscle weakness, headache, bruising or pain near the injection site, and swelling. If a patient is allergic, a reaction may also occur. More serious side effects can occur but are rare. If you experience any unusual side effects, contact our doctor or your primary care doctor.

While the time may vary depending on the symptoms, most side effects should dissipate within a few hours to a few days.

While you may notice results within the first few days, it typically takes up to a week to achieve the full effect.

Botox injections will last anywhere from three to six months.

To maintain your best results, it’s recommended that you receive injections every four to six months.

When done correctly, Botox looks very natural.

If you’re ready to experience the magic of Botox, make an appointment with Gotox today! First time customers will receive an introductory price of $10/unit for Botox and $570 for Juvaderm lip fillers.