Latisse
Generic Name: bimatoprost
Dosage Form: ophthalmic solution
Medically reviewed on Jul 1, 2017
Indications and Usage for Latisse
Latisse® (bimatoprost ophthalmic solution) 0.03% is indicated to treat hypotrichosis of the eyelashes by increasing their growth including length, thickness and darkness.
Latisse Dosage and Administration
Ensure the face is clean, makeup and contact lenses are removed. Once nightly, place one drop of Latisse®(bimatoprost ophthalmic solution) 0.03% 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. Dispose of the applicator after one use. Repeat for the opposite eyelid margin using a new sterile applicator.
Do not reuse applicators and do not use any other brush/applicator to apply Latisse®.
Do not apply to the lower eyelash line [see Warnings and Precautions (5.3, 5.4) and Patient Counseling Information (17)].
Additional applications of Latisse® will not increase the growth of eyelashes.
Upon discontinuation of treatment, eyelash growth is expected to return to its pre-treatment level.
Dosage Forms and Strengths
Bimatoprost ophthalmic solution 0.3 mg/mL.
Contraindications
Latisse® is contraindicated in patients with hypersensitivity to bimatoprost or to any of the ingredients [see Adverse Reactions (6.2)].
Warnings and Precautions
Effects on Intraocular Pressure
Bimatoprost ophthalmic solution (LUMIGAN®) 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, Latisse®lowered IOP, however, the magnitude of the reduction was not cause for clinical concern.
In ocular hypertension studies with LUMIGAN®, 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 LUMIGAN® or other prostaglandin analogs for the treatment of elevated intraocular pressure, 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 [see Patient Counseling Information (17)].
Iris Pigmentation
Increased iris pigmentation has occurred when bimatoprost solution was administered. Patients should be advised about the potential for increased brown iris pigmentation which is likely to be permanent [see Adverse Reactions (6.2) and Patient Counseling Information (17)].
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 Latisse® solution can be continued in patients who develop noticeably increased iris pigmentation.
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 (17)].
Hair Growth Outside the Treatment Area
There is the potential for hair growth to occur in areas where Latisse® solution comes in repeated contact with the skin surface. It is important to apply Latisse® 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 Latisse® from the eyelid margin to avoid it running onto the cheek or other skin areas [see Patient Counseling Information (17)].
Intraocular Inflammation
Latisse® solution should be used with caution in patients with active intraocular inflammation (e.g., uveitis) because the inflammation may be exacerbated.
Macular Edema
Macular edema, including cystoid macular edema, has been reported during treatment with bimatoprost ophthalmic solution (LUMIGAN®) for elevated IOP. Latisse® 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.
Contamination of Latisse® or Applicators
The Latisse® bottle must be kept intact during use. It is important to use Latisse® solution as instructed, by placing one drop on the single-use-per-eye 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 on one eye 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 (17)].
Use with Contact Lenses
Latisse® contains benzalkonium chloride, which may be absorbed by and cause discoloration of soft 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 (17)].
Adverse Reactions
The following adverse reactions are described elsewhere in the labeling:
· Effects on Intraocular Pressure [see Warnings and Precautions (5.1)]
· Iris Pigmentation [see Warnings and Precautions (5.2)]
· Lid Pigmentation [see Warnings and Precautions (5.3)]
· Hair Growth Outside the Treatment Area [see Warnings and Precautions (5.4)]
· Intraocular Inflammation [see Warnings and Precautions (5.5)]
· Macular Edema [see Warnings and Precautions (5.6)]
· Hypersensitivity [see Contraindications (4)]
Clinical Trial Experience
The following information is based on clinical trial results from a multicenter, double-masked, randomized, vehicle-controlled, parallel study including 278 adult patients for four months of treatment.
The most frequently reported adverse reactions were eye pruritus, conjunctival hyperemia, skin hyperpigmentation, ocular irritation, dry eye symptoms, and periorbital erythema. These reactions occurred in less than 4% of patients. Additional adverse reactions seen in clinical trials experience include foreign body sensation, hair growth abnormal, and iris hyperpigmentation.
Additional adverse reactions reported with bimatoprost ophthalmic solution (LUMIGAN®) for the reduction of intraocular pressure include, ocular dryness, visual disturbance, ocular burning, eye pain, blepharitis, cataract, superficial punctate keratitis, eye discharge, tearing, photophobia, allergic conjunctivitis, asthenopia, conjunctival edema, iritis, infections (primarily colds and upper respiratory tract infections), headaches, and asthenia.
Postmarketing Experience
The following adverse reactions have been identified during postapproval use of Latisse®. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure. The reactions include: dry skin of the eyelid and/or periocular area, eye swelling, eyelid edema, hypersensitivity (local allergic reactions), 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 and erythematous), skin discoloration (periorbital), and vision blurred.
USE IN SPECIFIC POPULATIONS
Pregnancy
Risk Summary
There are no adequate and well-controlled studies of Latisse (bimatoprost ophthalmic solution) 0.03% administration in pregnant women. There is no increase in the risk of major birth defects or miscarriages based on bimatoprost postmarketing experience.
In embryofetal development studies, administration of bimatoprost to pregnant mice and rats during organogenesis, resulted in abortion and early delivery at oral doses at least 33 times (mice) or 94 times (rats) the human exposure following topical ophthalmic administration of bimatoprost 0.03% to the cornea or conjunctival sac bilaterally once daily, based on the area under the curve (AUC). These adverse effects were not observed at 2.6 times (mice) and 47 times (rats) the human exposure following topical ophthalmic administration of bimatoprost 0.03% to the cornea or conjunctival sac bilaterally once daily, based on AUC.
In pre/postnatal development studies, administration of bimatoprost to pregnant rats from organogenesis to the end of lactation resulted in reduced gestation length and fetal body weight, and increased fetal and pup mortality at oral doses at least 41 times the human systemic exposure following topical ophthalmic administration of bimatoprost 0.03% to the cornea or conjunctival sac bilaterally once daily, based on AUC. No adverse effects were observed in rat offspring at exposures estimated at 14 times the human exposure following topical ophthalmic administration of bimatoprost 0.03% to the cornea or conjunctival sac bilaterally once daily , based on AUC.
Because animal reproductive studies are not always predictive of human response Latisse 0.03% should be administered during pregnancy only if the potential benefit justifies the potential risk to the fetus.
Data
Animal Data
In an embryofetal development rat study, abortion was observed in pregnant rats administered bimatoprost orally during organogenesis at 0.6 mg/kg/day (94 times the human systemic exposure following topical ophthalmic administration of bimatoprost 0.03% to the cornea or conjunctival sac bilaterally once daily , based on AUC. The No Observed Adverse Effect Level (NOAEL) for abortion was 0.3 mg/kg/day (estimated at 47 times the human systemic exposure following topical ophthalmic administration of bimatoprost 0.03% to the cornea or conjunctival sac bilaterally once daily based on AUC). No abnormalities were observed in rat fetuses at doses up to 0.6 mg/kg/day.
In an embryofetal development mouse study, abortion and early delivery were observed in pregnant mice administered bimatoprost orally during organogenesis at doses greater than or equal to 0.3 mg/kg/day (33 times the human systemic exposure following topical ophthalmic administration of bimatoprost 0.03% to the cornea or conjunctival sac bilaterally once daily , based on AUC). The NOAEL for abortion and early delivery was 0.1 mg/kg/day (2.6 times the human systemic exposure following topical ophthalmic administration of bimatoprost 0.03% to the cornea or conjunctival sac bilaterally once daily, based on AUC) . No abnormalities were observed in mouse fetuses at doses up to 0.6 mg/kg/day (72 times the human systemic exposure following topical ophthalmic administration of bimatoprost 0.03% to the cornea or conjunctival sac bilaterally once daily, based on AUC).
In a pre/postnatal development study, treatment of pregnant rats with bimatoprost orally from gestation day 7 to lactation day 20 resulted in reduced gestation length, increased late resorptions, fetal deaths, and postnatal pup mortality, and reduced pup body weight at doses greater than or equal to 0.3 mg/kg/day. These effects were observed at exposures at least 41 times the human systemic exposure following topical ophthalmic administration of bimatoprost 0.03% to the cornea or conjunctival sac bilaterally once daily, based on AUC). The NOAEL for postnatal development and mating performance of the offspring was 0.1 mg/kg/day (estimated at 14 times the human systemic exposure following topical ophthalmic administration of bimatoprost 0.03% to the cornea or conjunctival sac bilaterally once daily, based on AUC).
Lactation
Risk Summary
It is not known whether topical ocular treatment with Latisse 0.03% could result in sufficient systemic absorption to produce detectable quantities in human milk. In animal studies, bimatoprost has been shown to be present in breast milk of lactating rats at an intravenous dose (i.e., 1 mg/kg) 324 times the recommended human ophthalmic dose (on a mg/m2 basis), however no animal data is available at clinically relevant doses.
The developmental and health benefits of breastfeeding should be considered along with the mother's clinical need for Latisse 0.03% and any potential adverse effects on the breastfed child from Latisse0.03%.
Pediatric Use
Use of Latisse® was evaluated in a sixteen week double-masked, randomized, vehicle-controlled study conducted in pediatric patients who were post-chemotherapy or had alopecia areata, and adolescents who had hypotrichosis with no associated medical condition. No new safety issues were observed. The results of the Global Eyelash Assessment are provided in Table 1.
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Table 1. Number (%) of subjects with at least a 1-grade increase from baseline at month 4 in Global Eyelash Assessment
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Age Range
(years)
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Latisse®
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Vehicle
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Difference (95% CI)
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Adolescents with hypotrichosis (N=40)
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15 - 17
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19/26 (73%)
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1/14 (7%)
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66% (44%, 88%)
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Post Chemotherapy Pediatric Patients (N=16)
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5 - 17
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11/13 (85%)
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3/3 (100%)
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-15% (-35%, 4%)
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Alopecia Areata Pediatric Patients (N=15)
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5 - 17
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4/9 (44%)
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2/6 (33%)
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11% (-39%, 61%)
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Geriatric Use
No overall clinical differences in safety or effectiveness have been observed between elderly and other adult patients.
Latisse Description
Latisse® (bimatoprost ophthalmic solution) 0.03% 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. Latisse® is a clear, isotonic, colorless, sterile ophthalmic solution with an osmolality of approximately 290 mOsmol/kg.
Contains: Active: bimatoprost 0.3 mg/mL; Preservative: benzalkonium chloride 0.05 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.
Latisse - Clinical Pharmacology
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.
Pharmacokinetics
Absorption
After one drop of bimatoprost ophthalmic solution 0.03% 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.
Nonclinical Toxicology
Carcinogenesis, Mutagenesis, Impairment of Fertility
Carcinogenesis
Bimatoprost was not carcinogenic in either mice or rats when administered by oral gavage for 104 weeks at doses up to 2 mg/kg/day and 1 mg/kg/day, respectively (192 and 291 times the human systemic exposure following topical ophthalmic administration of bimatoprost 0.03% to the cornea or conjunctival sac bilaterally once daily based on blood AUC levels.
Mutagenesis
Bimatoprost was not mutagenic or clastogenic in the Ames test, in the mouse lymphoma test, or in the in vivo mouse micronucleus tests.
Impairment of Fertility
Bimatoprost did not impair fertility in male or female rats up to doses of 0.6 mg/kg/day (103 times the human systemic exposure following topical ophthalmic administration of bimatoprost 0.03% to the cornea or conjunctival sac bilaterally once daily based on blood AUC levels.
Clinical Studies
Latisse® solution was evaluated for its effect on overall eyelash prominence in a multicenter, double-masked, randomized, vehicle-controlled, parallel study including 278 adult patients for four months of treatment. The primary efficacy endpoint in this study was an increase in overall eyelash prominence as measured by at least a 1-grade increase on the 4-point Global Eyelash Assessment (GEA) scale, from baseline to the end of the treatment period (week 16). Latisse® was more effective than vehicle as measured by the GEA score, with statistically significant differences seen at 8-week, 12-week, and 16-week (primary endpoint) treatment durations.
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Table 2. Number (%) of subjects with at least a 1-grade increase from baseline in Global Eyelash Assessment (Primary Efficacy Endpoint – Week 16)
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Week
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Latisse®
N=137
N (%)
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Vehicle
N=141
N (%)
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1
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7 (5%)
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3 (2%)
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4
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20 (15%)
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11 (8%)
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8
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69 (50%)
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21 (15%)
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12
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95 (69%)
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28 (20%)
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16
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107 (78%)
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26 (18%)
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20
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103 (79%)
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27 (21%)
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In this study, patients were also evaluated for the effect of Latisse® solution on the length, thickness and darkness of their eyelashes. Improvements from baseline in eyelash growth as measured by digital image analysis assessing eyelash length, fullness/thickness, and darkness were statistically significantly more pronounced in the bimatoprost group at weeks 8, 12, and 16.
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Table 3
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* a negative value is representative of eyelash darkening
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Efficacy endpoint at Week 16
(Mean Change from Baseline)
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Latisse®
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Vehicle
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Eyelash growth (length)
(mm; % increase)
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N=137
1.4; 25%
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N=141
0.1; 2%
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Fullness/thickness
(mm2; % increase)
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N=136
0.7; 106%
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N=140
0.1; 12%
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Eyelash darkness (intensity*; % increase in darkness)
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N=135
-20.2; -18%
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N=138
-3.6; -3%
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After the 16-week treatment period, a 4-week post-treatment period followed during which the effects of bimatoprost started to return toward baseline. The effect on eyelash growth is expected to abate following longer term discontinuation.
How Supplied/Storage and Handling
Latisse® (bimatoprost ophthalmic solution) 0.03% is supplied sterile in opaque white low density polyethylene dispenser bottles and tips with turquoise polystyrene caps accompanied by sterile, disposable applicators:
3 mL in a 5 mL bottle with 70 applicators NDC 0023-3616-70
5 mL in a 5 mL bottle with 140 applicators NDC 0023-3616-05
Storage: Store at 2°-25°C (36°-77°F).
Patient Counseling Information
Advise the patient to read the FDA-approved patient labeling (Patient Information).
Nightly Application
Inform patients that Latisse® (bimatoprost ophthalmic solution) 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 Latisse®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 Latisse® solution gets into the eye proper, it will not cause harm. The eye should not be rinsed.
Additional applications of Latisse® will not increase the growth of eyelashes.
Inform patients 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. Counsel patients that the effect is not permanent and can be expected to gradually return to the original level upon discontinuation of treatment with Latisse®.
Handling the Bottle and Applicator
Instruct patients that the Latisse® 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. Instruct patients to only use the applicator supplied with the product once and then discard since reuse could result in using a contaminated applicator. Serious infections may result from using contaminated solutions or applicators.
Potential for Intraocular Pressure Effects
Latisse® may lower intraocular pressure although not to a level that will cause clinical harm.
In patients using LUMIGAN® or other prostaglandin analogs for the treatment of elevated intraocular pressure, the concomitant use of Latisse® may interfere with the desired reduction in IOP. Patients using prostaglandin analogs for IOP reduction should only use Latisse® after consulting with their physician.
Potential for Eyelid Skin Darkening
Inform patients about the possibility of eyelid skin darkening, which may be reversible after discontinuation of Latisse®.
Potential for Iris Darkening
Advise patients about the potential for increased brown iris pigmentation which is likely to be permanent. Increased iris pigmentation has occurred when bimatoprost solution was administered.
Potential for Unexpected Hair Growth or Eyelash Changes
Inform patients of the possibility of hair growth occurring outside of the target treatment area if Latisse®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.
When to Seek Physician Advice
Advise patients 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 Latisse®. Patients on IOP-lowering medications should not use Latisse® without prior consultation with their physician.
Use with Contact Lenses
Advise patients that Latisse® solution contains benzalkonium chloride, which may be absorbed by and cause discoloration of soft contact lenses. Contact lenses should be removed prior to application of Latisse® and may be reinserted 15 minutes following its administration.
© 2017 Allergan. All rights reserved.
All trademarks are the property of their respective owners.
Patented. See: www.allergan.com/patents
Irvine, CA 92612
Made in the U.S.A.
72303US17
------Cut---Here---✂-------------------------------------------------------------------------------------------------------------
FDA-approved Patient Labeling
PATIENT INFORMATION
Latisse® [la teece]
(bimatoprost ophthalmic solution) 0.03%
Read the Patient Information that comes with Latisse® 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 Latisse® solution?
Latisse® solution is a prescription treatment for hypotrichosis used to grow eyelashes, making them longer, thicker and darker.
Who should NOT take Latisse®?
Do not use Latisse® solution if you are allergic to one of its ingredients.
Are there any special warnings associated with Latisse® use?
Latisse® solution is intended for use on the skin of the upper eyelid margins at the base of the eyelashes. Refer to Illustration 2 below. DO NOT APPLY to the lower eyelid. If you are using LUMIGAN®or other products in the same class for elevated intraocular pressure (IOP), or if you have a history of abnormal IOP, you should only use Latisse® under the close supervision of your physician.
Latisse® use may cause darkening of the eyelid skin which may be reversible. Latisse® use may also cause increased brown pigmentation of the colored part of the eye which is likely to be permanent.
It is possible for hair growth to occur in other areas of your skin that Latisse® 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 Latisse®.
Who should I tell that I am using Latisse®?
You should tell your physician you are using Latisse® especially if you have a history of eye pressure problems.
You should also tell anyone conducting an eye pressure screening that you are using Latisse®.
What should I do if I get Latisse® in my eye?
Latisse® solution is an ophthalmic drug product. Latisse® is not expected to cause harm if it gets into the eye proper. Do not attempt to rinse your eye in this situation.
What are the possible side effects of Latisse®?
The most common side effects after using Latisse® solution are an itching sensation in the eyes and/or eye redness. This was reported in approximately 4% of patients. Latisse® solution may cause other less common side effects which typically occur on the skin close to where Latisse® is applied, or in the eyes. These 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 Latisse®solution.
What happens if I stop using Latisse®?
If you stop using Latisse®, 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 is NOT expected to reverse and is likely permanent.
How do I use Latisse®?
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 Latisse® on the area of the applicator closest to the tip but not on the tip (see Illustration 1). 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 (see Illustration 2). Blot any excess solution beyond the eyelid margin. Dispose of the applicator after one use.
Repeat for the opposite upper eyelid margin using a new sterile applicator. This helps minimize any potential for contamination from one eyelid to another.
Illustration 1
Illustration 2
DO NOT APPLY in your eye or to the lower lid. ONLY use the sterile applicators supplied with Latisse® to apply the product. If you miss a dose, don't try to “catch up.” Just apply Latisse® solution the next evening. Fifty percent of patients treated with Latisse® in a clinical study saw significant improvement by 2 months after starting treatment.
If any Latisse® 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 Latisse® and may be reinserted 15 minutes following its administration.
Use of Latisse® more than once a day will not increase the growth of eyelashes more than use once a day.
Store Latisse® solution at 36°-77°F (2°-25°C).
General Information about Latisse®
Prescription treatments are sometimes prescribed for conditions that are not mentioned in patient information leaflets. Do not use Latisse® solution for a condition for which it was not prescribed. Do not give Latisse® to other people. It may not be appropriate for them to use.
This leaflet summarizes the most important information about Latisse® solution. If you would like more information, talk with your physician. You can also call Allergan's product information department at 1-800-678-1605.
What are the ingredients in Latisse®?
Active ingredient: bimatoprost
Inactive ingredients: benzalkonium chloride; 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.
© 2017 Allergan. All rights reserved.
All trademarks are the property of their respective owners.
Patented. See: www.allergan.com/patents
Irvine, CA 92612
Made in the U.S.A.
72303US17
NDC 0023-3616-70
Latisse ®
(bimatoprost ophthalmic
solution) 0.03%
Rx only
STERILE R
ALLERGAN
Contents:
One 3 mL bottle of sterile solution
70 disposable applicators
|
Latisse bimatoprost solution/ drops
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Product Information
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Product Type
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HUMAN PRESCRIPTION DRUG LABEL
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Item Code (Source)
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NDC:0023-3616
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Route of Administration
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OPHTHALMIC
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DEA Schedule
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|
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Active Ingredient/Active Moiety
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Ingredient Name
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Basis of Strength
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Strength
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bimatoprost (bimatoprost)
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bimatoprost
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0.3 mg in 1 mL
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Inactive Ingredients
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Ingredient Name
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Strength
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benzalkonium chloride
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|
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sodium chloride
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sodium phosphate, dibasic
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|
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citric acid monohydrate
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water
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Packaging
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#
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Item Code
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Package Description
|
|
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1
|
NDC:0023-3616-04
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1 BOTTLE, DROPPER in 1 CARTON
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|
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1
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3 mL in 1 BOTTLE, DROPPER
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2
|
NDC:0023-3616-03
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1 BOTTLE, DROPPER in 1 CARTON
|
|
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2
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3 mL in 1 BOTTLE, DROPPER
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3
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NDC:0023-3616-81
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1 BOTTLE, DROPPER in 1 CARTON
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3
|
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3 mL in 1 BOTTLE, DROPPER
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4
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NDC:0023-3616-16
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1 BOTTLE, DROPPER in 1 CARTON
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|
|
4
|
|
1.5 mL in 1 BOTTLE, DROPPER
|
|
|
5
|
NDC:0023-3616-80
|
1 BOTTLE, DROPPER in 1 CARTON
|
|
|
5
|
|
3 mL in 1 BOTTLE, DROPPER
|
|
|
6
|
NDC:0023-3616-05
|
1 BOTTLE, DROPPER in 1 CARTON
|
|
|
6
|
|
5 mL in 1 BOTTLE, DROPPER
|
|
|
7
|
NDC:0023-3616-70
|
1 BOTTLE, DROPPER in 1 CARTON
|
|
|
7
|
|
3 mL in 1 BOTTLE, DROPPER
|
|
|
8
|
NDC:0023-3616-71
|
1 BOTTLE, DROPPER in 1 CARTON
|
|
|
8
|
|
3 mL in 1 BOTTLE, DROPPER
|
|
|
|
|
|
Marketing Information
|
|
Marketing Category
|
Application Number or Monograph Citation
|
Marketing Start Date
|
Marketing End Date
|
|
NDA
|
NDA022369
|
01/26/2009
|
|
|
|
Labeler - Allergan, Inc. (144796497)
|
|
Establishment
|
|
Name
|
Address
|
ID/FEI
|
Operations
|
|
Allergan, Inc.
|
|
362898611
|
MANUFACTURE(0023-3616)
|
Allergan, Inc.
