Boost Your Client’s Confidence with Allergan® Aesthetics LATISSE®: The Revolutionary Eyelash Treatment

LATISSE®: A Scientific Approach to Eyelash Growth

⚠️ Important Safety Information: LATISSE® (bimatoprost ophthalmic solution) 0.03% is a prescription treatment for hypotrichosis used to grow eyelashes, making them longer, thicker, and darker. Common side effects include eye itching or redness. LATISSE® may cause darkening of the eyelid skin, which may be reversible, and increased brown pigmentation of the colored part of the eye, which is likely permanent. Hair growth outside the treatment area may occur if the solution is repeatedly applied to surrounding skin. LATISSE® should be used under the supervision of a licensed medical provider and in accordance with the FDA-approved Prescribing Information.

In the world of aesthetic medicine, LATISSE® by Allergan® Aesthetics stands out as the first and only FDA-approved prescription treatment for hypotrichosis of the eyelashes — a condition characterized by inadequate or insufficient lashes. This groundbreaking ophthalmic solution harnesses the power of bimatoprost, a prostaglandin analog, to stimulate the eyelash growth cycle and deliver measurable, visible results.

Disclaimer: LATISSE® is a registered trademark of Allergan, Inc., an AbbVie company.

By lengthening the anagen (growth) phase of the hair cycle, LATISSE® helps patients achieve longer, thicker, and darker eyelashes over time. It has proven especially effective for individuals with sparse, short, or thinning lashes, enabling them to enhance their appearance naturally and boost self-confidence.

For healthcare professionals, offering LATISSE® means providing a clinically proven, FDA-approved solution to meet growing patient demand for effective, natural-looking eyelash enhancement.

Understanding LATISSE®

What is LATISSE®?

LATISSE® is a prescription-only treatment developed by Allergan® Aesthetics to improve eyelash growth in adults with inadequate lashes. Its active ingredient, bimatoprost ophthalmic solution, was originally developed for ocular hypertension. During clinical use, researchers observed a remarkable secondary effect: significant eyelash growth — leading to the development and FDA approval of LATISSE® for cosmetic use.

Patients using LATISSE® under the supervision of a licensed professional can expect noticeable improvement in the length, thickness, and darkness of their eyelashes, typically within a structured 16-week treatment period.

How LATISSE® Works: The Science Behind It

Bimatoprost, the active compound in LATISSE®, prolongs the anagen phase of the eyelash hair cycle — increasing both the number of hairs in this growth phase and the duration of the phase itself. This dual mechanism results in denser, longer, and more pigmented eyelashes over time. Clinical studies have confirmed that with consistent application, LATISSE® provides significant improvement by the 16-week mark.

For medical and aesthetic professionals, understanding the pharmacological action of bimatoprost is key to educating patients, setting realistic expectations, and ensuring adherence to treatment protocols.

Benefits of LATISSE®

Clinically Proven Results

In FDA-reviewed clinical studies, patients using LATISSE® demonstrated measurable improvements in lash length, thickness, and darkness over 16 weeks of consistent use. Results are gradual and dependent on patient compliance and individual response.

Boosting Patient Confidence

Patients who achieve noticeable enhancement of their eyelashes often report increased self-esteem and confidence, both in professional and social settings. Many also appreciate the reduced need for mascara or false lashes, aligning with today’s preference for natural beauty.

By empowering patients to enhance their natural features, LATISSE® promotes a sense of autonomy and self-care that extends beyond physical appearance.

Application Process: How to Use LATISSE®

Step-by-Step Application Instructions

1. Preparation
   • Wash the face thoroughly and remove all makeup.
   • Remove contact lenses before application.
2. Application
   • Place one drop of LATISSE® solution on the sterile, single-use applicator.
   • Apply evenly to the base of the upper lash line only.
   • Blot any excess solution with a clean tissue.
   • Use a new sterile applicator for the other eye.
3. Post-Application
   • Do not rinse the eye area.
   • Reinsert contact lenses only after at least 15 minutes.
   • Wash hands after application.

Professional Guidance and Safety Considerations

• Prescription Requirement:
  LATISSE® is available only by prescription. Providers must assess the patient’s suitability and monitor use to prevent inappropriate application.
• Role of Healthcare Providers:
  Providers educate patients about correct usage, set expectations for gradual results, and manage any adverse effects.
• Potential Side Effects:
  Mild itching, redness, and darkening of the eyelid skin may occur. Rarely, unwanted hair growth outside the application area can result if the product spreads beyond the lash line. Patients should promptly report significant side effects to their provider.

⚠️ Fair Balance Callout Like all prescription treatments, LATISSE® carries potential risks and side effects. Common adverse reactions include itching, redness, and darkening of the eyelid skin. In rare cases, increased iris pigmentation has been reported. LATISSE® should only be prescribed and supervised by trained, licensed professionals, and patients should carefully follow the FDA-approved Prescribing Information.

Addressing Hypotrichosis with LATISSE®

What is Hypotrichosis?

Hypotrichosis refers to having less hair than normal in one or more hair-bearing areas of the body. While it can affect any area, it is particularly noticeable — and often distressing — when it involves the eyelashes or eyebrows.

Eyelash hypotrichosis describes inadequate or insufficient lashes, which can impact both appearance and function. Beyond aesthetics, eyelashes protect the eyes from dust, debris, and foreign particles. Reduced lash density compromises this barrier, increasing the risk of irritation and potential eye infections.

Hypotrichosis may be congenital (present at birth) or acquired later in life due to factors such as trauma, medical treatments, or underlying health conditions.

LATISSE® as a Solution for Eyelash Hypotrichosis

For individuals affected by eyelash hypotrichosis, LATISSE® (bimatoprost ophthalmic solution) offers a clinically proven, FDA-approved treatment. Believed to extend the growth phase of the eyelash cycle, LATISSE® promotes longer, thicker, and darker lashes — improving both aesthetic appearance and functional protection.

In clinical studies, patients typically noticed visible improvements in lash length, density, and pigmentation within 16 weeks of consistent use. However, individual results may vary, and proper supervision by a licensed healthcare professional is critical to ensure safety and maximize efficacy.

Important Considerations When Prescribing LATISSE®

While LATISSE® is effective, it is essential to counsel patients about possible risks and set realistic expectations:

Clinical Background

• LATISSE® was developed after bimatoprost — originally used to treat high intraocular pressure (e.g., glaucoma) — was observed to stimulate eyelash growth as a side effect. The 2012 FDA Prescribing Information provides an early reference to its approved uses and precautions.”

Possible Side Effects

• Iris Pigmentation: LATISSE® may cause permanent brown darkening of the colored part of the eye.
• Eyelid Skin Darkening: Reversible darkening of the eyelid skin may occur.
• Unintended Hair Growth: Hair may grow outside the treatment area if the solution comes into contact with adjacent skin.
• Return to Baseline: If treatment is discontinued, lashes gradually return to their previous state over time.

Professional Supervision

• LATISSE® is available by prescription only. Healthcare providers should evaluate patients for contraindications (e.g., allergy to ingredients) and educate them on proper use.
• Setting realistic expectations helps patients remain compliant with the 16-week regimen and minimizes the risk of misuse.

Pipeline Medical: Your Source for Competitive LATISSE® Pricing

Why Choosing the Right Supplier Matters

When offering LATISSE® in your practice, sourcing authentic, FDA-approved product from a trusted distributor is critical. Counterfeit or mishandled products not only compromise patient outcomes but also expose practices to regulatory and reputational risks.

How Pipeline Medical Supports Your Practice

Pipeline Medical is a single-source medical supply partner, combining the roles of Group Purchasing Organization (GPO), distributor, and material manager. This unique structure allows aesthetic practices to save time, reduce costs, and operate more efficiently — without sacrificing product authenticity or quality.

Exclusive Allergan® Aesthetics Program

Pipeline Medical’s partnership with Allergan® Aesthetics provides practices access to elite LATISSE® pricing — equivalent to the rates enjoyed by practices purchasing directly from Allergan® at high-volume tiers (e.g., $500,000 practices).

Benefits of Partnering with Pipeline Medical

• Significant Cost Savings: Practices benefit from Pipeline Medical’s aggregated buying power, reducing costs while maintaining healthy margins.
• Streamlined Procurement: Simplified ordering and inventory management reduce administrative workload.
• Instant Access to Elite Pricing: Practices gain a competitive edge with immediate access to top-tier LATISSE® pricing, helping them stay ahead in a dynamic aesthetic market.

By partnering with Pipeline Medical, clinics can offer LATISSE® at competitive rates while ensuring product authenticity, regulatory compliance, and efficient operations — ultimately enhancing patient care and satisfaction.

⚠️ Fair Balance Callout LATISSE® carries potential risks, including darkening of the iris, eyelid skin darkening, unintended hair growth outside the treatment area, and gradual return of lashes to baseline upon discontinuation. Outcomes depend on practitioner expertise, patient compliance, and adherence to guidelines. Always refer to the full FDA Prescribing Information and ensure treatments are supervised by licensed healthcare professionals after informed consent.

Frequently Asked Questions (FAQs) About LATISSE®

What is LATISSE®, and what makes it unique?

LATISSE® is the first and only FDA-approved prescription treatment for hypotrichosis of the eyelashes (inadequate or insufficient lashes). Developed by Allergan® Aesthetics, it has been clinically proven to enhance eyelash growth by extending the active growth phase, resulting in longer, thicker, and darker lashes.

How does LATISSE® work?

LATISSE® prolongs the anagen (growth) phase of the eyelash hair cycle. This extends the duration of growth and increases the number of lashes growing at any given time, improving both lash density and appearance.

How do I use LATISSE® correctly?

• Begin by cleaning your face and removing makeup and contact lenses.
• Place one drop of LATISSE® on the sterile applicator provided.
• Apply it along the skin at the base of the upper lash line (not the lower lash line), moving from the inner corner outward.
• Use a new applicator for each eye to avoid contamination.
• Avoid letting the bottle tip or applicator touch any surfaces.

Do I need a prescription to use LATISSE®?

Yes. LATISSE® is a prescription medication that requires evaluation by a licensed healthcare provider to ensure it is appropriate and safe for use.

When can I expect to see results?

Most patients notice visible improvement in 8–12 weeks, with full results typically seen at 16 weeks when used consistently as directed. Individual results may vary.

What are the potential side effects of LATISSE®?

Common side effects may include:

• Itching or redness of the eyelids
• Eyelid skin darkening (usually reversible)
• Darkening of the iris (likely permanent)
• Hair growth outside the treatment area if misapplied
• Eye discomfort if solution enters the eye

Patients should report any unusual or concerning symptoms to their provider promptly.

Can I use LATISSE® if I am allergic to its ingredients?

No. Patients with known allergies to any components of LATISSE® should not use it. If you suspect an allergic reaction, discontinue use and seek medical attention.

What precautions should I take while using LATISSE®?

• Do not let the applicator or bottle tip touch surfaces to prevent contamination.
• Remove contact lenses before application and wait at least 15 minutes before reinserting them.
• Avoid applying LATISSE® to areas outside the upper lash line.

How can Pipeline Medical help with LATISSE® procurement?

Pipeline Medical provides competitive, elite-tier pricing for LATISSE® through its exclusive Allergan® Aesthetics program — pricing typically reserved for high-volume purchasers. Their services ensure you receive authentic, FDA-approved products with transparent pricing and dependable delivery.

Why choose Pipeline Medical for LATISSE®?

Pipeline Medical combines the roles of Group Purchasing Organization (GPO), distributor, and material manager to streamline your procurement. Practices save time and money while ensuring consistent access to premium Allergan® products like LATISSE®.

Conclusion: Elevating Client Confidence with LATISSE®

LATISSE® offers a scientifically validated, FDA-approved solution for clients with insufficient lashes, delivering longer, thicker, and darker eyelashes that can significantly boost self-esteem and confidence. By incorporating LATISSE® into your practice, you empower clients to embrace their natural beauty and enjoy a more confident appearance.

For practitioners, LATISSE® represents an opportunity to offer a clinically proven, high-demand service. Its strong safety and efficacy profile, when prescribed and supervised correctly, makes it a valuable addition to any aesthetic offering.

Partnering with Pipeline Medical further enhances this offering by ensuring your practice benefits from competitive pricing, authentic products, and streamlined procurement — allowing you to focus on delivering exceptional care.

⚠️ Fair Balance Callout Like all prescription medications, LATISSE® carries potential risks. Common side effects include eyelid redness, irritation, and possible darkening of the iris or eyelid skin. Misuse may lead to hair growth outside the intended area. Always refer to the FDA-approved Prescribing Information, and ensure treatment is supervised by a licensed healthcare professional following informed consent.

For elite pricing and reliable access to LATISSE® and the full range of Allergan® Aesthetics products, contact Pipeline Medical today to learn more about their exclusive program and elevate your practice.

The information provided here is for educational purposes only and does not replace clinical training, medical judgment, or professional advice. Always consult the full Prescribing Information and ensure that LATISSE® is used appropriately and safely under the supervision of a licensed healthcare provider.