Reimbursement

IHEEZO is the only FDA-approved topical ocular anesthetic with a permanent J-code and transitional pass through status.

This allows for separate payment for Medicare Fee-for-Service patients in the ASC/HOPD setting and in the physician office setting.

Reimbursement Guide

Ordering

IHEEZO may be ordered from any of the following wholesalers/distributors.

Ordering and reimbursement are supported by a dedicated Reimbursement Business Manager through our Harrow Cares program (see more information below).

Need help with insurance and out-of-pocket costs?

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Seamless Enrollment & Coverage

Offers simplified enrollment for benefit investigation and coverage verification. Get alerts when a PA is required, or proceed directly—order, treat, and submit for reimbursement.

Copay & Product Assurance

Enroll in our commercial copay program, foundation research, or patient assistance based on need. Receive product replacement for breakage, spoilage, or loss—when you treat, you’re covered.**

**Subject to program terms and limitations. Please contact 1-866-HROWINC (476-9462) for additional details.

Commercial

Copay Program

  • Available to commercially insured patients. Excludes Medicaid, Medicare, Tricare, etc.
  • Pay as little as $0
  • Program Maximum Annual Benefit: $5,000
  • Program Enrollment Period: Start Date through December 31 of that calendar year
  • Once enrolled, a claim should be submitted within 180 days of the treatment date
  • Treatments within the last 120 days may qualify for retroactive copay assistance. Enroll immediately with an Enrollment Form and insurer EOB.

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.