Flarex
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Flarex
- Generic name
- FLUOROMETHOLONE ACETATE
- Manufacturer
- Eyevance Pharmaceuticals
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 19918ea5-8568-44d6-b8ee-7b2197cee85c
- SPL ID
- 2bed0334-e39e-c18b-e063-6294a90af598
- Version
- 7
- Effective date
- 2025-01-17
- Source export date
- 2026-09-28
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:24:50
| Harmonized routes |
|---|
| OPHTHALMIC |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application applno | NDA | 019079 | derived:openfda.application_number |
| application number | NDA019079 | openfda.application_number | |
| brand name | Flarex | openfda.brand_name | |
| generic name | FLUOROMETHOLONE ACETATE | openfda.generic_name | |
| manufacturer name | Eyevance Pharmaceuticals | openfda.manufacturer_name | |
| ndc | package | 71776-100-05 | openfda.package_ndc |
| ndc | package | 71776-100-03 | openfda.package_ndc |
| ndc | product | 71776-100 | openfda.product_ndc |
| ndc11 | package | 71776010003 | derived:openfda.package_ndc |
| ndc11 | package | 71776010005 | derived:openfda.package_ndc |
| rxcui | 1249631 | openfda.rxcui | |
| rxcui | 1249629 | openfda.rxcui | |
| spl id | 2bed0334-e39e-c18b-e063-6294a90af598 | id | |
| spl set id | 19918ea5-8568-44d6-b8ee-7b2197cee85c | set_id | |
| unii | 9I50C3I3OK | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
WARNINGS FOR TOPICAL OPHTHALMIC USE. NOT FOR INJECTION. Use in the treatment of herpes simplex infection requires great caution. Prolonged use may result in glaucoma, damage to the optic nerve, defect in visual acuity and visual field, cataract formation and/or may aid in the establishment of secondary ocular infections from pathogens due to suppression of host response. Acute purulent infections of the eye may be masked or exacerbated by presence of steroid medication. Topical ophthalmic corticosteroids may slow corneal wound healing. In those diseases causing thinning of the cornea or sclera, perforation has been known to occur with chronic use of topical steroids. If these products are used for 10 days or longer, intraocular pressure (IOP) should be routinely monitored even though it may be difficult in children and uncooperative patients.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS Glaucoma with optic nerve damage, visual acuity and field defects, cataract formation, secondary ocular infection following suppression of host response, and perforation of the globe may occur. Postmarketing Experience The following reaction has been identified during post-marketing use of FLAREX ® (fluorometholone acetate ophthalmic suspension) 0.1% in clinical practice. Because reactions are reported voluntarily from a population of unknown size, estimates of frequency cannot be made. The reaction, which has been chosen for inclusion due to either its seriousness, frequency of reporting, possible causal connection to FLAREX, or a combination of these factors, includes: dysgeusia. The following rare adverse reactions have been reported: Cushing's syndrome and adrenal suppression may occur after very frequent use of topical ophthalmic corticosteroids, particularly in very young children.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.