ZIRGAN
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
- ZIRGAN
- Generic name
- GANCICLOVIR
- Manufacturer
- Bausch & Lomb Incorporated
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- ea25e7ac-7a93-4ec8-975b-2cec197e1c27
- SPL ID
- 52207853-4445-f142-e063-6394a90a281c
- Version
- 15
- Effective date
- 2026-05-18
- Source export date
- 2026-10-12
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:28:37
| 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 | 022211 | derived:openfda.application_number |
| application number | NDA022211 | openfda.application_number | |
| brand name | ZIRGAN | openfda.brand_name | |
| generic name | GANCICLOVIR | openfda.generic_name | |
| manufacturer name | Bausch & Lomb Incorporated | openfda.manufacturer_name | |
| ndc | package | 24208-535-35 | openfda.package_ndc |
| ndc | package | 24208-535-32 | openfda.package_ndc |
| ndc | package | 24208-535-15 | openfda.package_ndc |
| ndc | product | 24208-535 | openfda.product_ndc |
| ndc11 | package | 24208053532 | derived:openfda.package_ndc |
| ndc11 | package | 24208053535 | derived:openfda.package_ndc |
| ndc11 | package | 24208053515 | derived:openfda.package_ndc |
| rxcui | 388052 | openfda.rxcui | |
| rxcui | 864650 | openfda.rxcui | |
| spl id | 52207853-4445-f142-e063-6394a90a281c | id | |
| spl set id | ea25e7ac-7a93-4ec8-975b-2cec197e1c27 | set_id | |
| unii | P9G3CKZ4P5 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
5 WARNINGS AND PRECAUTIONS ZIRGAN is indicated for topical ophthalmic use only. ( 5.1 ) Patients should not wear contact lenses if they have signs or symptoms of herpetic keratitis or during the course of therapy with ZIRGAN. ( 5.2 ) 5.1 Topical Ophthalmic Use Only ZIRGAN is indicated for topical ophthalmic use only. 5.2 Avoidance of Contact Lenses Patients should not wear contact lenses if they have signs or symptoms of herpetic keratitis or during the course of therapy with ZIRGAN. 5.3 Risk of Contamination Do not allow the tip of the container to touch any surface, as this may contaminate the ointment. If pain develops, or if redness, itching, or inflammation becomes aggravated, the patient should be advised to consult a physician.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
6 ADVERSE REACTIONS Most common adverse reactions reported in patients were blurred vision (60%), eye irritation (20%), punctate keratitis (5%), and conjunctival hyperemia (5%). Most common adverse reactions were blurred vision (60%), eye irritation (20%), punctate keratitis (5%), and conjunctival hyperemia (5%). ( 6 ) To report SUSPECTED ADVERSE REACTIONS, contact Bausch & Lomb Incorporated, at 1-800-553-5340 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.