MEMBRANEBLUE
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
- MEMBRANEBLUE
- Generic name
- TRYPAN BLUE
- Manufacturer
- Dutch Ophthalmic Research Center (International) B.V.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 0364aceb-dd3f-4bac-b468-25379a07ccfc
- SPL ID
- 44559f09-e0e2-a332-e063-6394a90aa296
- Version
- 17
- Effective date
- 2025-11-24
- Source export date
- 2026-09-28
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:08:54
| 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 | 022278 | derived:openfda.application_number |
| application number | NDA022278 | openfda.application_number | |
| brand name | MEMBRANEBLUE | openfda.brand_name | |
| generic name | TRYPAN BLUE | openfda.generic_name | |
| manufacturer name | Dutch Ophthalmic Research Center (International) B.V. | openfda.manufacturer_name | |
| ndc | package | 68803-672-05 | openfda.package_ndc |
| ndc | product | 68803-672 | openfda.product_ndc |
| ndc11 | package | 68803067205 | derived:openfda.package_ndc |
| spl id | 44559f09-e0e2-a332-e063-6394a90aa296 | id | |
| spl set id | 0364aceb-dd3f-4bac-b468-25379a07ccfc | set_id | |
| unii | I2ZWO3LS3M | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
MembraneBlue 0.15% - Warnings and precautions section Excessive Staining Excess MembraneBlue 0.15% should be immediately removed from the eye after staining. Priming of the Syringe To make sure the plunger moves smoothly before use, first retract the plunger or twist the plunger in a clockwise motion before injecting the fluid. Excessive Staining: Excess MembraneBlue 0.15% should be immediately removed from the eye after staining. Priming of the Syringe: To make sure the plunger moves smoothly before use, first retract the plunger or twist the plunger in a clockwise motion before injecting the fluid.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
MembraneBlue 0.15% - Adverse reactions section Adverse reactions reported following use of MembraneBlue 0.15% 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. Most common adverse reactions include discoloration of high water content hydrogen intraocular lenses and inadvertent staining of the posterior lens capsule and vitreous face. To report SUSPECTED ADVERSE REACTIONS contact Dutch Ophthalmic, 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.