Dry Eye Test
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
- Dry Eye Test
- Generic name
- FLUORESCEIN SODIUM
- Manufacturer
- Nomax Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 04866053-f973-471e-b3bc-241fb76303a2
- SPL ID
- 7490418c-b489-4b90-bc3d-33ed71231e2d
- Version
- 3
- Effective date
- 2019-12-23
- Source export date
- 2026-10-12
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/fb14b8f3d34b45230a84f851c029385f512adf3f002423a9b78d4f7ca626ecec/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:23:23
| 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 | Dry Eye Test | openfda.brand_name | |
| generic name | FLUORESCEIN SODIUM | openfda.generic_name | |
| manufacturer name | Nomax Inc. | openfda.manufacturer_name | |
| ndc | package | 51801-008-15 | openfda.package_ndc |
| ndc | product | 51801-008 | openfda.product_ndc |
| ndc11 | package | 51801000815 | derived:openfda.package_ndc |
| spl id | 7490418c-b489-4b90-bc3d-33ed71231e2d | id | |
| spl set id | 04866053-f973-471e-b3bc-241fb76303a2 | set_id | |
| unii | 93X55PE38X | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.