May 6, 2018

Eyelash Enhancement

Discover the benefits of Latisse!

With Latisse®, you can finally grow your own eyelashes… darker, fuller and longer than ever before!  Latisse® is the first and only FDA-approved eyelash growth serum for women and men with thin or sparse eyelashes.  In just a few weeks of regular Latisse®use, lashes appear:

  • Darker
  • Fuller
  • Longer
  • Thicker

The quick and simple once-daily application of Latisse® eyelash growth to the base of the upper eyelashes is all that it takes to grow more beautiful long lashes. Latisse® users can experience thicker, more youthful eyelashes in as little as six weeks, with full results in 16 weeks. To maintain the results, continued eyelash growth treatment with Latisse® is recommended. Latisse® is recommended even if eyelash extensions are used to promote healthy lash growth and give lash extensions structure to fill.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

LATISSE® (bimatoprost ophthalmic solution) 0.03% Important Information Indication

LATISSE® (bimatoprost ophthalmic solution) 0.03% is indicated to treat hypotrichosis of the eyelashes by increasing their growth, including length, thickness, and darkness.

Important Safety Information
Contraindications: LATISSE® is contraindicated in patients with hypersensitivity to bimatoprost or to any

of the ingredients.

Warnings and Precautions: In patients using LUMIGAN® (bimatoprost ophthalmic solution) or other prostaglandin analogs for the treatment of elevated intraocular pressure (IOP), the concomitant use of LATISSE® may interfere with the desired reduction in IOP. Patients using prostaglandin analogs including LUMIGAN® for IOP reduction should only use LATISSE® after consulting with their physician and should be monitored for changes to their intraocular pressure.

Increased iris pigmentation has occurred when bimatoprost solution was administered. Patients should be advised about the potential for increased brown iris pigmentation, which is likely to be permanent.

Bimatoprost has been reported to cause pigment changes (darkening) to periorbital pigmented tissues and eyelashes.

There is the potential for hair growth to occur in areas where LATISSE® solution comes in repeated contact with skin surfaces. Apply LATISSE® only to the skin of the upper eyelid margin at the base of the eyelashes.

LATISSE® solution should be used with caution in patients with active intraocular inflammation (eg, uveitis) because the inflammation may be exacerbated. LATISSE® should be used with caution in aphakic patients, in pseudophakic patients with a torn posterior lens capsule, or in patients with known risk factors for macular edema.

Adverse Reactions: The most frequently reported adverse reactions were eye pruritus, conjunctival hyperemia, skin hyperpigmentation, ocular irritation, dry eye symptoms, and periorbital erythema. These reactions occurred in less than 4% of patients.

Postmarketing Experience: The following adverse reactions have been identified during postapproval use of LATISSE®: dry skin of the eyelid and/or periocular area, eye swelling, eyelid edema, hypersensitivity (local allergic reactions), lacrimation increased, madarosis and trichorrhexis (temporary loss of a few eyelashes to loss of sections of eyelashes, and temporary eyelash breakage, respectively), periorbital and lid changes associated with a deepening of the eyelid sulcus, rash (including macular and erythematous), skin discoloration (periorbital), and vision blurred.

For more information on LATISSE®, please see the accompanying full Prescribing Information.