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Latisse® is the only FDA-approved prescription treatment for inadequate or sparse eyelashes, a condition known as eyelash hypotrichosis.
Its active ingredient is bimatoprost 0.03%, a prostaglandin analog that was originally developed to treat glaucoma under the brand name Lumigan®.
Latisse works by affecting the natural eyelash growth cycle. It:
Most people begin noticing results within 4 to 8 weeks, with full results typically appearing after 12 to 16 weeks of consistent use.
With nightly application, patients can expect:
Keep in mind that results require ongoing use. If you stop applying Latisse, your eyelashes will gradually return to their original appearance over the next few months.
Latisse is the FDA-approved option specifically indicated for eyelash growth.
Benefits include:
Its main drawback is that it is typically the most expensive option.
Lumigan contains the same active ingredient, bimatoprost, usually in concentrations of 0.01% or 0.03%.
Although FDA-approved for glaucoma—not eyelash growth—it is sometimes prescribed off-label for cosmetic lash enhancement.
Advantages include:
However:
Compounded lash serums have become increasingly popular in aesthetic practices because they allow providers to customize treatment based on a patient's needs.
Common compounded formulations include:
Latisse is generally well tolerated, but patients should be aware of potential side effects, including:
For the safest and most effective results:
We offer both FDA-approved and customized treatment options based on your goals, sensitivity, and budget.
For patients seeking the gold-standard treatment, Latisse® remains our preferred recommendation. For others, a compounded bimatoprost formula may provide excellent results while offering additional conditioning ingredients and greater flexibility.