C20H10Na2O5 Fluorescein Sodium Ophthalmic Strips
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
- C20H10Na2O5 Fluorescein Sodium Ophthalmic Strips
- Generic name
- FLUORESCEIN SODIUM
- Manufacturer
- Vistamerica USA
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 292abb69-84ad-4f61-e063-6394a90a1447
- SPL ID
- 386aaf96-81c0-bd6f-e063-6394a90ad761
- Version
- 2
- Effective date
- 2025-06-01
- Source export date
- 2026-10-12
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:47:33
| 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 |
|---|---|---|---|
| brand name | C20H10Na2O5 Fluorescein Sodium Ophthalmic Strips | openfda.brand_name | |
| generic name | FLUORESCEIN SODIUM | openfda.generic_name | |
| manufacturer name | Vistamerica USA | openfda.manufacturer_name | |
| ndc | package | 83851-100-30 | openfda.package_ndc |
| ndc | package | 83851-100-10 | openfda.package_ndc |
| ndc | package | 83851-100-05 | openfda.package_ndc |
| ndc | product | 83851-100 | openfda.product_ndc |
| ndc11 | package | 83851010030 | derived:openfda.package_ndc |
| ndc11 | package | 83851010010 | derived:openfda.package_ndc |
| ndc11 | package | 83851010005 | derived:openfda.package_ndc |
| spl id | 386aaf96-81c0-bd6f-e063-6394a90ad761 | id | |
| spl set id | 292abb69-84ad-4f61-e063-6394a90a1447 | set_id | |
| unii | 93X55PE38X | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.