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Designed for comfortable delivery with HYDRELLA® 1,2

HYDRELLA is comprised of glycerin and hydroxypropyl methylcellulose (HPMC), ingredients commonly found in lubricant drops1,3

Comfort score data in adult and pediatric patients2

COMFORT STUDY DESIGN: Results from a Phase 3, multicenter, randomized, double-masked, vehicle-controlled, parallel-group, long-term safety and tolerability study in 512 adult and pediatric (aged 2 to 17) patients receiving ZERVIATE® or vehicle with BID dosing. Drop comfort was self-assessed by patients immediately upon instillation, 30 seconds post dose, and 1 minute post dose using an 11-point scale (0=very comfortable, 10=very uncomfortable).2

Approximately 21% of children and 20% of adults report experiencing ocular allergy symptoms year-round4

Available as single-unit containers for dosing convenience

Administered as a single drop, twice daily approximately 8 hours apart1

  • Store at 15°C to 25°C (59°F to 77°F)1
Find out more about the safety profile of ZERVIATE

INDICATIONS AND USAGE

ZERVIATE® (cetirizine ophthalmic solution) 0.24% is a histamine-1 (H1) receptor antagonist indicated for treatment of ocular itching associated with allergic conjunctivitis.

DOSAGE AND ADMINISTRATION

Instill one drop of ZERVIATE in each affected eye twice daily (approximately 8 hours apart).

IMPORTANT SAFETY INFORMATION

WARNINGS AND PRECAUTIONS

Contamination of Tip and Solution: As with any eye drop, care should be taken not to touch the eyelids or surrounding areas with the dropper tip of the bottle or tip of the single-use container to avoid injury to the eye and to prevent contaminating the tip and solution. Keep the multi-dose bottle closed when not in use. Discard the single-use container after using in each eye.

Contact Lens Wear: Patients should be advised not to wear a contact lens if their eye is red. ZERVIATE should not be instilled while wearing contact lenses. Remove contact lenses prior to instillation of ZERVIATE. The preservative in ZERVIATE, benzalkonium chloride, may be absorbed by soft contact lenses. Lenses may be reinserted 10 minutes following administration of ZERVIATE.

ADVERSE REACTIONS

The most commonly reported adverse reactions occurred in approximately 1%–7% of patients treated with either ZERVIATE or vehicle. These reactions were ocular hyperemia, instillation site pain, and visual acuity reduced.

Please see the full Prescribing Information.

References: 1. ZERVIATE [package insert]. Fort Worth, TX: Eyevance Pharmaceuticals LLC; 2020. 2. Malhotra RP, Meier E, Torkildsen G, et al. Safety of cetirizine ophthalmic solution 0.24% for the treatment of allergic conjunctivitis in adult and pediatric subjects. Clin Ophthalmol. 2019;13:403-413. 3. Electronic Code of Federal Regulations. Part 349: Ophthalmic drug products for over-the-counter human use. Accessed February 12, 2021. https://www.ecfr.gov/cgi-bin/text-idx?SID=50adb5289f382ac0919186d53a10e0af&mc=true&node=pt21.5.349&rgn=div5#se21.5.349_13. 4. Meltzer EO, Farrar JR, Sennett C. Findings from an online survey assessing the burden and management of seasonal allergic rhinoconjunctivitis in US patients. J Allergy Clin Immunol Pract. 2017;5:779-789.

IMPORTANT SAFETY INFORMATION

WARNINGS AND PRECAUTIONS

Contamination of Tip and Solution: As with any eye drop, care should be taken not to touch the eyelids or surrounding areas with the dropper tip of the bottle or tip of the single-use container to avoid injury to the eye and to prevent contaminating the tip and solution. Keep the multi-dose bottle closed when not in use. Discard the single-use container after using in each eye.

Contact Lens Wear: Patients should be advised not to wear a contact lens if their eye is red. ZERVIATE should not be instilled while wearing contact lenses. Remove contact lenses prior to instillation of ZERVIATE. The preservative in ZERVIATE, benzalkonium chloride, may be absorbed by soft contact lenses. Lenses may be reinserted 10 minutes following administration of ZERVIATE.

ADVERSE REACTIONS

The most commonly reported adverse reactions occurred in approximately 1%–7% of patients treated with either ZERVIATE or vehicle. These reactions were ocular hyperemia, instillation site pain, and visual acuity reduced.

Please see the full Prescribing Information.