FULL PRESCRIBING INFORMATION

1 INDICATIONS AND USAGE

LASHÀNCE (bimatoprost ophthalmic solution) 0.01% is indicated to treat hypotrichosis of the eyelashes by increasing their growth including length, thickness and darkness.

2 DOSAGE AND ADMINISTRATION

Ensure the face is clean, makeup and contacts are removed. Once nightly, place one drop of LASHÀNCE (bimatoprost ophthalmic solution) 0.01% on the disposable sterile applicator supplied with the package and apply evenly along the skin of the upper eyelid margin at the base of the eyelashes. The upper lid margin in the area of lash growth should feel lightly moist without runoff. Blot any excess solution runoff outside the upper eyelid margin with a tissue or other absorbent cloth. Repeat for the opposite eyelid margin. Dispose of the applicator after use.

DO NOT reuse applicators and DO NOT use any other brush/applicator to apply LASHÀNCE.

DO NOT apply to the lower eyelash line [see Warnings and Precautions (5.4) and Patient Counseling Information (11.1)].

Additional applications of LASHÀNCE will not increase the growth of eyelashes.

Upon discontinuation of treatment, eyelash growth is expected to return to its pre-treatment level.

3 DOSAGE FORMS AND STRENGTHS

Bimatoprost ophthalmic solution 0.1 mg/mL.

4 CONTRAINDICATIONS

None

5 WARNINGS AND PRECAUTIONS

5.1 Effects on Intraocular Pressure

Bimatoprost ophthalmic solution lowers intraocular pressure (IOP) when instilled directly to the eye in patients with elevated IOP. In clinical trials, in patients with or without elevated IOP, placement of bimatoprist ophthamomic solution on the lids lowered IOP, however, the magnitude of the reduction was not cause for clinical concern.

In ocular hypertension studies with bimatoprost, it has been shown that exposure of the eye to more than one dose of bimatoprost daily may decrease the intraocular pressure lowering effect. In patients using or other prostaglandin analogs for the treatment of elevated intraocular pressure, the concomitant use of LASHÀNCE may interfere with the desired reduction in IOP. Patients using prostaglandin analogs including for IOP reduction should only use LASHÀNCE after consulting with their physician and should be monitored for changes to their intraocular pressure [see Patient Counseling Information (11.3)].

5.2 Iris Pigmentation

Increased iris pigmentation has occurred when bimatoprost solution was administered. Patients should be advised about the potential for increased brown iris pigmentation [see Adverse Reactions (6.1) and Patient Counseling Information (11.5)].

The pigmentation change is due to increased melanin content in the melanocytes rather than to an increase in the number of melanocytes. The long term effects of increased pigmentation are not known. Iris color changes seen with administration of bimatoprost ophthalmic solution may not be noticeable for several months to years.

Typically, the brown pigmentation around the pupil spreads concentrically towards the periphery of the iris and the entire iris or parts of the iris become more brownish. Neither nevi nor freckles of the iris appear to be affected by treatment. Treatment with LASHÀNCEsolution can be continued in patients who develop noticeably increased iris pigmentation.

5.3 Lid Pigmentation

Bimatoprost has been reported to cause pigment changes (darkening) to periorbital pigmented tissues 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 [see Patient Counseling Information (11.4)].

5.4 Hair Growth Outside the Treatment Area

There is the potential for hair growth to occur in areas where LASHÀNCE comes in repeated contact with the skin surface. It is important to apply LASHÀNCE only to the skin of the upper eyelid margin at the base of the eyelashes using the accompanying sterile applicators, and to carefully blot any excess LASHÀNCE from the eyelid margin to avoid it running onto the cheek or other skin areas [see Patient Counseling Information (11.6)].

5.5 Intraocular Inflammation

LASHÀNCE should be used with caution in patients with active intraocular inflammation (e.g., uveitis) because the inflammation may be exacerbated.

5.6 Macular Edema

Macular edema, including cystoid macular edema, has been reported during treatment with bimatoprost ophthalmic solution for elevated IOP.  LASHÀNCE  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.

5.7 Contamination of LASHÀNCE or Applicators

The LASHÀNCE bottle must be kept intact during use. It is important to use LASHÀNCE as instructed, by placing one drop on the single-use applicator. The bottle tip should not be allowed to contact any other surface since it could become contaminated. The accompanying sterile applicators should only be used one time and then discarded since reuse of applicators increases the potential for contamination and infections. There have been reports of bacterial keratitis associated with the use of multiple-dose containers of topical ophthalmic products [see Patient Counseling Information (11.2)].

5.8 Use with Contact Lenses

Contact lenses should be removed prior to application of solution and may be reinserted 15 minutes following its administration [see Patient Counseling Information (11.8)].

6 ADVERSE REACTIONS

6.1 Postmarketing Experience

The following reactions have been identified during use of LASHÀNCE in clinical practice. Because they are reported voluntarily from a population of unknown size, estimates of frequency cannot be made. The reactions, which have been chosen for inclusion due to either their seriousness, frequency of reporting, possible causal connection to LASHÀNCE, or a combination of these factors, include: burning sensation (eyelid), eye swelling, eyelid irritation, eyelid edema, eyelids pruritus, iris hyperpigmentation, lacrimation increased, madarosis and trichorrhexis (temporary loss of a few lashes 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, erythematous, and pruritic limited to the eyelids and periorbital region), skin discoloration (periorbital), and vision blurred.

7 USE IN SPECIFIC POPULATIONS

7.1 Pregnancy

Pregnancy Category C

Teratogenic effects: In embryo/fetal developmental studies in pregnant mice and rats, abortion was observed at oral doses of bimatoprost which achieved at least 33 or 97 times, respectively, the maximum intended human exposure (based on blood AUC levels after topical ophthalmic administration to the cornea or conjunctival sac). At doses at least 41 times the maximum intended human exposure, the gestation length was reduced in the dams, the incidence of dead fetuses, late resorptions, peri- and postnatal pup mortality was increased, and pup body weights were reduced. There are no adequate and well-controlled studies of bimatoprost ophthalmic solution 0.01% administration in pregnant women. Because animal reproductive studies are not always predictive of human response, LASHÀNCE should be administered during pregnancy only if the potential benefit justifies the potential risk to the fetus.

7.2 Nursing Mothers

It is not known whether LASHÀNCE is excreted in human milk, although in animal studies, bimatoprost has been shown to be excreted in breast milk. Because many drugs are excreted in human milk, caution should be exercised when LASHÀNCE is administered to a nursing woman.

7.3 Pediatric Use

Safety and effectiveness in pediatric patients have not been established.

7.4 Geriatric Use

No overall clinical differences in safety or effectiveness have been observed between elderly and other adult patients.

11 DESCRIPTION

LASHÀNCE (bimatoprost ophthalmic solution) 0.01% is a synthetic prostaglandin analog. Its chemical name is (Z)-7-[(1R,2R,3R,5S)-3,5-Dihydroxy-2-[(1E,3S)-3-hydroxy-5-phenyl-1-pentenyl]cyclopentyl]-N-ethyl-5- heptenamide, and its molecular weight is 415.58. Its molecular formula is C25H37NO4. Its chemical structure is:

Bimatoprost is a powder, which is very soluble in ethyl alcohol and methyl alcohol and slightly soluble in water. LASHÀNCE is a clear, isotonic, colorless, sterile ophthalmic solution with an osmolality of approximately 290 mOsmol/kg.

Contains: Active: bimatoprost 0.1 mg/mL; Inactives: sodium chloride; sodium phosphate, dibasic; citric acid; and purified water. Sodium hydroxide and/or hydrochloric acid may be added to adjust pH. The pH during its shelf life ranges from 6.8 – 7.8.

8 CLINICAL PHARMACOLOGY

8.1 Mechanism of Action

Bimatoprost is a structural prostaglandin analog. Although the precise mechanism of action is unknown the growth of eyelashes is believed to occur by increasing the percent of hairs in, and the duration of the anagen or growth phase.

8.2 Pharmacokinetics

Absorption

After one drop of bimatoprost ophthalmic solution 0.01% was administered once daily into both eyes (cornea and/or conjunctival sac) of 15 healthy subjects for two weeks, blood concentrations peaked within 10 minutes after dosing and were below the lower limit of detection (0.025 ng/mL) in most subjects within 1.5 hours after dosing. Mean Cmax and AUC0-24hr values were similar on days 7 and 14 at approximately 0.08 ng/mL and 0.09 ng*hr/mL, respectively, indicating that steady state was reached during the first week of ocular dosing. There was no significant systemic drug accumulation over time.

Distribution

Bimatoprost is moderately distributed into body tissues with a steady-state volume of distribution of 0.67 L/kg. In human blood, bimatoprost resides mainly in the plasma. Approximately 12% of bimatoprost remains unbound in human plasma.

Metabolism

Bimatoprost is the major circulating species in the blood once it reaches the systemic circulation. Bimatoprost then undergoes oxidation, N-deethylation, and glucuronidation to form a diverse variety of metabolites.

Elimination

Following an intravenous dose of radiolabeled bimatoprost (3.12 mcg/kg) to six healthy subjects, the maximum blood concentration of unchanged drug was 12.2 ng/mL and decreased rapidly with an elimination half-life of approximately 45 minutes. The total blood clearance of bimatoprost was 1.5 L/hr/kg. Up to 67% of the administered dose was excreted in the urine while 25% of the dose was recovered in the feces.

9 NONCLINICAL TOXICOLOGY

9.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

Bimatoprost was not carcinogenic in either mice or rats when administered by oral gavage at doses of up to 2 mg/kg/day and 1 mg/kg/day respectively (approximately 192 and 291 times the recommended human exposure based on blood AUC levels after topical corneal and/or conjunctival sac administration respectively) for 104 weeks. Bimatoprost was not mutagenic or clastogenic in the Ames test, in the mouse lymphoma test, or in the in vivo mouse micronucleus tests. Bimatoprost did not impair fertility in male or female rats up to doses of 0.6 mg/kg/day.

10 HOW SUPPLIED/STORAGE AND HANDLING

LASHÀNCE (bimatoprost ophthalmic solution) 0.01% is supplied sterile in opaque white low density air tight polyethylene dispenser bottles and tips with turquoise polystyrene caps accompanied by sterile, disposable applicators:

5 mL in a 5 mL bottle with 70 applicators NDC 71384-0541-05

Storage: LASHÀNCE should be stored at 2°-25°C (36°-77°F).

11 PATIENT COUNSELING INFORMATION

11.1 Nightly Application

Patients should be informed that LASHÀNCE (bimatoprost ophthalmic solution) 0.01% should be applied every night using only the accompanying sterile applicators. They should start by ensuring their face is clean, all makeup is removed, and their contact lenses removed (if applicable). Then, carefully place one drop of LASHÀNCE solution on the disposable sterile applicator and brush cautiously along the skin of the upper eyelid margin at the base of the eyelashes. If any LASHÀNCE solution gets into the eye proper, it will not cause harm. The eye should not be rinsed.

Additional applications of LASHÀNCE will not increase the growth of eyelashes.

Patients should be informed not to apply to the lower eyelash line. Any excess solution outside the upper eyelid

margin should be blotted with a tissue or other absorbent material. The onset of effect is gradual but is not significant in the majority of patients until 2 months. Patients should be counseled that the effect is not permanent and can be expected to gradually return to the original level upon discontinuation of treatment with LASHÀNCE.

11.2 Handling the Bottle and Applicator

Patients should be instructed that the LASHÀNCE bottle must be maintained intact and to avoid allowing the tip of the bottle or applicator to contact surrounding structures, fingers, or any other unintended surface in order to avoid contamination of the bottle or applicator by common bacteria known to cause ocular infections. Patients should also be instructed to only use the applicator supplied with the product and then discard since reuse could result in using a contaminated applicator. Serious infections may result from using contaminated solutions or applicators.

11.3 Potential for Intraocular Pressure Effects

LASHÀNCE may lower intraocular pressure although not to a level that will cause clinical harm. In patients using prostaglandin analogs for the treatment of elevated intraocular pressure, the concomitant use of LASHÀNCE may interfere with the desired reduction in IOP. Patients using prostaglandin analogs for IOP reduction should only use LASHÀNCE after consulting with their physician.

11.4 Potential for Eyelid Skin Darkening

Patients should be informed about the possibility of eyelid skin darkening, which may be reversible after discontinuation of LASHÀNCE.

11.5 Potential for Iris Darkening

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

11.6 Potential for Unexpected Hair Growth or Eyelash Changes

Patients should be informed of the possibility of hair growth occurring outside of the target treatment area if LASHÀNCE repeatedly touches the same area of skin outside the treatment area. They should also be informed of the possibility of disparity between eyes in length, thickness, pigmentation, number of eyelashes or vellus hairs, and/or direction of eyelash growth. Eyelash changes are likely reversible upon discontinuation of treatment.

11.7 When to Seek Physician Advice

Patients should be advised that if they develop a new ocular condition (e.g., trauma or infection), experience a sudden decrease in visual acuity, have ocular surgery, or develop any ocular reactions, particularly conjunctivitis and eyelid reactions, they should immediately seek their physician’s advice concerning the continued use of LASHÀNCE. Patients on IOP-lowering medications should not use LASHÀNCE without prior consultation with their physician.

11.8 Use with Contact Lenses

Contact lenses should be removed prior to application of LASHÀNCE and may be reinserted 15 minutes following its administration.

PATIENT INFORMATION

Read the Patient Information that comes with LASHÀNCE before you start using it and each time you get a refill. There may be new information. This leaflet does not take the place of talking with your physician about your treatment.

What is hypotrichosis of the eyelashes?

Hypotrichosis is another name for having inadequate or not enough eyelashes.

What is LASHÀNCE?

LASHÀNCE is a prescription treatment for hypotrichosis used to grow eyelashes, making them bigger, thicker and fuller.

Who should NOT take LASHÀNCE?

DO NOT use LASHÀNCE solution if you are allergic to one of its ingredients.

Are there any special warnings associated with LASHÀNCE use?

LASHÀNCE is intended for use on the skin of the upper eyelid margins at the base of the eyelashes. DO NOT APPLY to the lower eyelid. If you are using products in the same class for elevated intraocular pressure (IOP), or if you have a history of abnormal IOP, you should only use LASHÀNCE under the close supervision of your physician.

LASHÀNCE use may cause darkening of the eyelid skin which may be reversible. LASHÀNCE use may also cause increased brown pigmentation of the colored part of the eye in rare cases. It is possible for hair growth to occur in other areas of your skin that LASHÀNCE frequently touches. Any excess solution outside the upper eyelid margin should be blotted with a tissue or other absorbent material to reduce the chance of this from happening. It is also possible for a difference in eyelash length, thickness, fullness, pigmentation, number of eyelash hairs, and/or direction of eyelash growth to occur between eyes. These differences, should they occur, will usually go away if you stop using LASHÀNCE. Other side effects may include skin darkening, eye irritation, dryness of the eyes, and redness of the eyelids. If you develop a new ocular condition (e.g., trauma or infection),experience a sudden decrease in visual acuity, have ocular surgery, or develop any ocular reactions, particularly conjunctivitis and eyelid reactions, you should immediately seek your physician’s advice concerning the continued use of LASHÀNCE solution.

Who should I tell that I am using LASHÀNCE?

You should tell your physician you are using LASHÀNCE especially if you have a history of eye pressure problems.

You should also tell anyone conducting an eye pressure screening that you are using LASHÀNCE.

What should I do if I get LASHÀNCE in my eye?

LASHÀNCE solution is an ophthalmic drug product. LASHÀNCE is not expected to cause harm if it gets into the eye proper. DO NOT attempt to rinse your eye in this situation.

What happens if I stop using LASHÀNCE?

If you stop using LASHÀNCE, your eyelashes are expected to return to their previous appearance over several weeks to months. Any eyelid skin darkening is expected to reverse after several weeks to months. Any darkening of the colored part of the eye known as the iris may reverse. In very rare cases it can be permanent.

How do I use LASHÀNCE?

The recommended dosage is one application nightly to the skin of the upper eyelid margin at the base of the eyelashes only. Once nightly, start by ensuring your face is clean, makeup and contact lenses are removed. Remove an applicator from its tray. Then, holding the sterile applicator horizontally, place one drop of LASHÀNCE on the area of the applicator closest to the tip but not on the tip. Then immediately draw the applicator carefully across the skin of the upper eyelid margin at the base of the eyelashes (where the eyelashes meet the skin) going from the inner part of your lash line to the outer part. Blot any excess solution beyond the eyelid margin. Repeat for the opposite upper eyelid margin.

DO NOT APPLY in your eye or to the lower lid. ONLY use the sterile applicators supplied with LASHÀNCE to apply the product. If you miss a dose, don’t try to “catch up.” Just apply LASHÀNCE the next evening.

If any LASHÀNCE solution gets into the eye proper, it is not expected to cause harm. The eye should not be rinsed.

Don’t allow the tip of the bottle or applicator to contact surrounding structures, fingers, or any other unintended surface in order to avoid contamination by common bacteria known to cause infections.

Contact lenses should be removed prior to application of LASHÀNCE and may be reinserted 15 minutes following its administration.

Use of LASHÀNCE more than once a day will not increase the growth of eyelashes more than use once a day. Store LASHÀNCE solution at 368°-77°F (2o-25°C).

 

General Information about LASHÀNCE

Prescription treatments are sometimes prescribed for conditions that are not mentioned in patient information leaflets. DO NOT use LASHÀNCE for a condition for which it was not prescribed. DO NOT give LASHÀNCE to other people. It may not be appropriate for them to use.

This prescribing WHAT WORD summarize the most important information about LASHÀNCE solution. If you would like more information, talk with your physician.

 

What are the ingredients in LASHÀNCE?

 

Active ingredient: bimatoprost

Inactive ingredients: sodium chloride; sodium phosphate monobasic; sodium phosphate dibasic; Poloxamer 184; Polysorbate-80. The pH during its shelf life ranges from 6.8 – 7.8.

 

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SAN DIEGO  CA 92103