VISIONBLUE
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
- VISIONBLUE
- Generic name
- TRYPAN BLUE
- Manufacturer
- D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- a44bc2ef-3d7f-4125-a7f7-c5969b1b4142
- SPL ID
- 4fa726e6-84c6-0f28-e063-6294a90aafe9
- Version
- 23
- Effective date
- 2026-04-17
- Source export date
- 2026-09-28
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:47:22
| Harmonized routes |
|---|
| INTRAOCULAR, 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 | 021670 | derived:openfda.application_number |
| application number | NDA021670 | openfda.application_number | |
| brand name | VISIONBLUE | openfda.brand_name | |
| generic name | TRYPAN BLUE | openfda.generic_name | |
| manufacturer name | D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. | openfda.manufacturer_name | |
| ndc | package | 68803-612-10 | openfda.package_ndc |
| ndc | product | 68803-612 | openfda.product_ndc |
| ndc11 | package | 68803061210 | derived:openfda.package_ndc |
| spl id | 4fa726e6-84c6-0f28-e063-6294a90aafe9 | id | |
| spl set id | a44bc2ef-3d7f-4125-a7f7-c5969b1b4142 | set_id | |
| unii | I2ZWO3LS3M | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings and Precautions Excessive staining : It is recommended that after injection all excess VisionBlue® 0.06% is immediately removed from the eye by thorough irrigation of the anterior chamber. Excessive staining : Excess VisionBlue® 0.06% should be removed from the eye immediately after staining.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
Adverse Reactions Adverse reactions reported following use of VisionBlue® 0.06% include discoloration of high water content hydrogen intraocular lenses ( see Contraindications ) and inadvertent staining of the posterior lens capsule and vitreous face. Staining of the posterior lens capsule or staining of the vitreous face is generally self limited, lasting up to one week. Inadvertent staining of the posterior lens capsule and vitreous face. To report SUSPECTED ADVERSE REACTIONS contact, Dutch Ophtalmic, USA at 1-800-75-DUTCH 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.