UPNEEQ®
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UPNEEQ® Non-surgical EYE LIFT

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With years of feedback, it’s become clear that this eyedrop is performing as promised by lifting low-lying, droopy lids.

  • In fact, in clinical trials 84% of patients report improvement in eyelid lift with Upneeq.

So whether they use it daily or want a refreshed look before an important work presentation or a date night, people with drooping eyelids are turning to Upneeq to give them more awake-looking eyes for the moments that matter.

Meet Upneeq® (oxymetazoline hydrochloride ophthalmic solution), 0.1%, the first and only FDA-approved prescription eye drop for adults with low-lying lids (also known as acquired blepharoptosis or ptosis).


  • It provides a non-surgical eye lift, quickly lifting eyelids for more awake-looking eyes.
  • Just one drop per eye, once daily, is clinically proven to give visible results — lifted and open eyelids in as fast as 5 minutes that can last up to 8 hours.
  • Say bye-bye to tired-looking eyelids, and hello to a more refreshed, awake-looking you.
  • If you have low-lying eyelids, find out if Upneeq is right for you.


Upneeq is the only FDA-approved prescription eyedrop for acquired ptosis (low-lying lids) that lifts your upper eyelids to open your eyes.

Love Your Lift!
20% OFF UPNEEQ®
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CONSULTATION IS REQUIRED PRIOR TO RECEIVING TREATMENT

$200.00

Upneeq is the only FDA-approved prescription eyedrop for acquired ptosis (low-lying lids) that lifts your upper eyelids to open your eyes

More Information
Benefits
  • Lifts eyelid(s) quickly
  • Most patients in clinical trials had a lift in their eyelids in as little as 2 hours
  • 84% of patients had some form of improvement
  • 74% of patients had more than a 50% improvement
  • In one study, some patients saw a lift in their eyelids as fast as 5 minutes after the first dose
  • Significantly improves upper field of vision
  • In clinical trials, Upneeq helped patients with acquired ptosis see more—on the first day of treatment!
  • 7.8% of patients had some form of improvement
  • 40.8% of patients had at least a 50% improvement on Day 14 (2 hours after applying Upneeq)
FAQs

What warnings and precautions are associated with UPNEEQ®?

  • Low-lying lids may be related to conditions such as stroke and/or brain aneurysm, Horner syndrome, myasthenia gravis, loss of the ability to move eye muscles, eye infection, and eye tumors. Tell your doctor if you have any of these conditions.
  • UPNEEQ® is a type of medication that may affect your blood pressure. If you have heart disease, uncontrolled high or low blood pressure, or feel faint at rest or when quickly standing up, you should call your doctor if your symptoms get worse.
  • Patients with reduced blood flow to the brain or heart, or patients who experience eye or mouth dryness due to an immune system disorder (Sjögren’s syndrome), should use care when taking UPNEEQ®. Call your doctor immediately if you feel your symptoms may be getting worse.
  • UPNEEQ® may increase the risk of eye pressure due to fluid buildup (angle-closure glaucoma) in patients with untreated narrow-angle glaucoma. Call your doctor immediately if you feel an increased pressure in your eye after using UPNEEQ®.

Do not let the tip of the UPNEEQ® vial touch your eye or any other surface. This can help prevent eye injury or contamination. Each UPNEEQ® vial is for one-time use and should be discarded after being used.

What are the most common side effects of UPNEEQ®?

The most common adverse reactions with UPNEEQ® (occurring in 1-5% of patients) were eye inflammation, eye redness, dry eye, blurred vision, eye pain at the time of use, eye irritation, and headache.

What should my doctor know about before prescribing me UPNEEQ®?

Your doctor should review your full medical history before prescribing UPNEEQ®.
UPNEEQ® belongs to a class of medications (alpha-adrenergic agonists) that may affect your blood pressure. Use UPNEEQ® carefully if you currently take an alpha-adrenergic agonist medication to treat heart disease or an enlarged prostate. Patients taking beta-blockers, or other medications to treat hypertension or an abnormal heartbeat, should also be careful when using UPNEEQ®.

Patients who use a certain class of antidepressant medication (monoamine oxidase inhibitors) should also be careful when using UPNEEQ®, as it may affect the way your body absorbs the medication.

These are not all of the possible side effects of UPNEEQ®. Tell your doctor if you have any side effect that bothers you or does not go away. Call your doctor for medical advice about side effects.

This is a summary of the most important safety information for UPNEEQ. For more in-depth safety information, please review the full Prescribing Information for UPNEEQ.

Size 30 Dropperette Single-use Drop Dispenser
Brand Upneeq

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How Do I Apply Upneeq®?

Apply Upneeq® to your affected eye(s) in 2 easy steps

Step 1: Cut open the foil wrapper and remove the single-use vial

Step 2: Apply one drop of Upneeq® in each affected eye as directed, once a day

Do not let the tip of the vial touch your eye or any other surface

  • Vials should not be re-used after opening and should be thrown away after applying drop(s)
  • If you wear contact lenses, remove them before applying Upneeq® eyedrops
  • You may put them back in 15 minutes after applying Upneeq®
  • If more than one topical ophthalmic drug is being used, the drugs should be administered at least 15 minutes between applications

Upneeq® should only be used as directed

  • Upneeq® is designed to only be applied as an eyedrop
  • Each vial contains enough Upneeq® solution to allow for one drop in each affected eye
  • The solution should never be swallowed or ingested in any other way Storage requirements:
  • Upneeq® should be stored at 68°F-77°F (20°C-25°C) and should be protected from excessive heat
  • Keep out of reach of children 

Each mL of UPNEEQ® (oxymetazoline hydrochloride ophthalmic solution) 0.1% contains 1 mg of oxymetazoline hydrochloride, equivalent to 0.09 mg (0.09%) of oxymetazoline free base. The ophthalmic solution contains the following inactive ingredients: calcium chloride, hydrochloric acid (used to adjust pH to 5.8 to 6.8), hypromellose, magnesium chloride, potassium chloride, sodium acetate, sodium chloride, sodium citrate, and water for injection.

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