Complete an online visit with a Rory-affiliated doctor or nurse practitioner and get Latisse delivered to your door. You’ll get free shipping, and you can pause or cancel your plan at any time. No questions asked.
Latisse® delivered to your door. Free 2-day shipping. Pause or cancel your plan at any time.
Medical evaluation and prescriptions by board-certified physicians & nurse practitioners
Secure handling of your personal data
Continued support from your doctor or nurse & our care team
Real people. Real results.
I ordered and received my order in just a couple of days! Easy, smooth process! Can’t wait for my lashes to grow!
“I’ve been using Latisse for six months now and as you can see—it really works. I’ll definitely keep using Latisse so I can maintain the look I have now. And Rory makes it super easy to continue with free 2-day shipping.”
This stuff works! My hairdresser just asked me if my lashes were real!
savannah.marie15 I was very impressed with how easy it is to navigate the Rory website and apply for approval for Latisse. I was able to complete the process in just a few minutes while in my lunch break at the office!
Just got my shipment of Latisse through Rory. 1,000 times more convenient than going to a doctor’s office. So glad I found this company
vanityandsuch I am SO excited to have long, voluminous lashes again! 😍 After hearing so many good things about @rory, I decided to kick off a trial using Latisse.
Latisse is absolutely amazing!! Saved my lashes after extensions!! I use it every day!!
The above opinions were shared by Rory members who were prescribed Latisse and received their medication at no cost.
Important Safety Information About Latisse®
Latisse is FDA approved for the treatment of thin or not enough eyelashes (eyelash hypotrichosis). Do not use Latisse if you are pregnant, possibly pregnant, or breastfeeding, if you are allergic to Latisse or its ingredients, or if you have glaucoma or are currently using medicated drops for glaucoma. Latisse may cause brown darkening of the colored part of the eye (iris) which is likely permanent or eyelid skin darkening which may be reversible. If discontinued, lashes gradually return to previous appearance. For more risk information, please read this important safety information.
What are the most important things I need to know about LATISSE®?
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 (brown darkening of the colored part of the eye) has occurred when bimatoprost solution was administered. Please be advised of the potential for increased brown iris pigmentation, which is likely to be permanent.
Bimatoprost has been reported to cause pigment changes (darkening) to the tissues around the eyes and eyelashes. The pigmentation is expected to increase as long as bimatoprost is administered, but has been reported to be reversible upon discontinuation of bimatoprost in most patients.
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. DO NOT APPLY LATISSE® to the lower lid.
LATISSE® solution should be used with caution in patients with active intraocular inflammation (eg, uveitis) because the inflammation may be exacerbated.
Who should not use LATISSE®?
Do not use LATISSE® if you:
Are allergic to one of the ingredients in LATISSE®
Are under 18 or if you are pregnant, trying to become pregnant or breastfeeding
If you use/used prescription products for eye pressure problems, use LATISSE® under your doctor’s care.
What are the most common side effects of LATISSE®?
In clinical trials of LATISSE®, the most frequently reported side effects were:
conjunctival hyperemia (redness of the eye)
skin hyperpigmentation (darkening of the skin)
dry eye symptoms
and erythema (redness) of the eyelid.
These adverse events occurred in less than 4% of participants.
Postmarketing Experience: The following reactions have been identified during postmarketing use of LATISSE® in clinical practice:
eyelid edema (swelling)
hypersensitivity (local allergic reactions)
increased tear production
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 (fold where the eyelid meets the lower eyebrow)
rash (including macular and erythematous)
skin discoloration around the eye (periorbital)
and vision blurred.
What is the FDA-approved use of LATISSE®?
LATISSE® (bimatoprost ophthalmic solution) 0.03% is indicated to treat hypotrichosis (thinning of the eyelashes) of the eyelashes by increasing their growth, including length, thickness, and darkness.
When should I call my primary provider?
Call your primary provider right away if you:
Experience a new eye condition (trauma or infection or injury)
Experience a sudden change/decrease in vision
Have eye surgery
Develop any eye reactions, especially eye redness and eyelid reactions
Develop any new symptom while on Latisse
Start a medication to lower the pressure in your eye. Patients on eye pressure lowering medications should not use Latisse without prior consultation with their eye physician.
If you are experiencing a medical emergency, call 911 or seek immediate medical attention.
What should I tell my Rory-affiliated provider before using LATISSE®?
Tell your Rory-affiliated provider all of the medications you are currently taking, if you are pregnant, planning to become pregnant, or breastfeeding, or if you have a history of:
Glaucoma or increased intraocular pressure
Have or have a history of macular edema
Have or have a history of intraocular inflammation
Have any other condition affecting your eyes
Have recently had a procedure on one or both eyes, including lasik surgery
Are using any intraocular medications
Withholding or providing inaccurate information about your health and medical history in order to obtain treatment may result in harm, including, in some cases, death.
You are encouraged to report negative side effects of prescription products to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088.