Safety

Coverage without compromise

Sterile,
single-use

Uniform
coverage5,6

Antiseptic
support7

Viscosity Matters

Novel low-viscosity gel for uniform coverage without antiseptic interference5-7

  • Avoids excess residue, supporting antiseptic effectiveness7
  • Reduces reliance on external applicators, minimizing potential ocular surface irritation5,6
  • Smooth, uniform coverage without excessive pooling or the need for redistribution5,6

Up to

less viscous than other FDA-approved topical ocular anesthetic gels.1,2,5,6

A randomized in-vivo study demonstrated IHEEZO® did not act as a barrier to the bactericidal actions of povidone-iodine 5%7

A recent study comparing IHEEZO and tetracaine ophthalmic solution 0.5% found that preservative-free chloroprocaine ophthalmic gel 3% achieved a 79.3% reduction in colony-forming units (CFU) versus 72.1% with tetracaine, demonstrating that IHEEZO does not inhibit the effectiveness of povidone-iodine.7

Rapid Results, Real Comfort2

IHEEZO works quickly to provide consistent, patient-reported pain reduction1

View Efficacy data

Key Safety Data

Sterile, single-use, and built for safety1

An established safety profile comparable to other topical ocular anesthetics1

IHEEZO is preservative-free and delivered in a sterile, single-use ampule for added patient safety.2 Single-use packaging may decrease the risk of infection and medication errors.8

Treatment-Emergent Adverse Events by Organ Class1

Two mild TEAEs were reported in the Tetracaine 0.5% group, while none were reported in the Chloroprocaine 3% Gel group.

Rapid metabolism

Chloroprocaine is a rapidly metabolized local anesthetic. In vitro half-life for IHEEZO is approximately 25 seconds.1

Rapid plasma degradation

The rapid plasma degradation of chloroprocaine greatly reduces the risk of systemic toxicity. In a clinical trial, chloroprocaine was undetectable in any plasma sample of any patient.1

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Approved Use

IHEEZO® is indicated for ocular surface anesthesia.

Important Safety Information

IHEEZO is contraindicated in patients with a history of hypersensitivity to any component of this preparation.

Approved Use

IHEEZO® is indicated for ocular surface anesthesia.

Important Safety Information

IHEEZO is contraindicated in patients with a history of hypersensitivity to any component of this preparation.

Approved Use

IHEEZO® is indicated for ocular surface anesthesia.

Important Safety Information

  • IHEEZO is contraindicated in patients with a history of hypersensitivity to any component of this preparation.
  • IHEEZO should not be injected or intraocularly administered.
  • Patients should not touch the eye for at least 10 to 20 minutes after using anesthetic as accidental injuries can occur due to insensitivity of the eye.
  • Prolonged use of a topical ocular anesthetic may produce permanent corneal opacification and ulceration with accompanying visual loss.
  • Do not touch the dropper tip to any surface as this may contaminate the gel.
  • IHEEZO is indicated for administration under the direct supervision of a healthcare provider. IHEEZO is not intended for patient self-administration.
  • The most common adverse reactions in studies following IHEEZO administration (incidence greater than or equal to 5%) were mydriasis, conjunctival hyperemia, and eye irritation.
  • You are encouraged to report suspected adverse reactions to the FDA. Visit www.fda.gov/medwatch, or call 1-800-FDA-1088.
  • For additional information about IHEEZO, please see the full Prescribing Information.

Approved Use

IHEEZO® is indicated for ocular surface anesthesia.

Important Safety Information

  • IHEEZO is contraindicated in patients with a history of hypersensitivity to any component of this preparation.
  • IHEEZO should not be injected or intraocularly administered.
  • Patients should not touch the eye for at least 10 to 20 minutes after using anesthetic as accidental injuries can occur due to insensitivity of the eye.
  • Prolonged use of a topical ocular anesthetic may produce permanent corneal opacification and ulceration with accompanying visual loss.
  • Do not touch the dropper tip to any surface as this may contaminate the gel.
  • IHEEZO is indicated for administration under the direct supervision of a healthcare provider. IHEEZO is not intended for patient self-administration.
  • The most common adverse reactions in studies following IHEEZO administration (incidence greater than or equal to 5%) were mydriasis, conjunctival hyperemia, and eye irritation.
  • You are encouraged to report suspected adverse reactions to the FDA. Visit www.fda.gov/medwatch, or call 1-800-FDA-1088.
  • For additional information about IHEEZO, please see the full Prescribing Information.