warnings
Warnings For external use only
BION TEARS
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
- BION TEARS
- Generic name
- DEXTRAN, HYPROMELLOSE
- Manufacturer
- Alcon Laboratories, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- e48d82f0-2f18-e514-4caa-e397d6713b99
- SPL ID
- 34aa9128-4bc4-45a6-aeae-a8c1f7699183
- Version
- 11
- Effective date
- 2023-12-14
- Source export date
- 2026-10-12
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:37:05
| 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 number | M018 | openfda.application_number | |
| brand name | BION TEARS | openfda.brand_name | |
| generic name | DEXTRAN, HYPROMELLOSE | openfda.generic_name | |
| manufacturer name | Alcon Laboratories, Inc. | openfda.manufacturer_name | |
| ndc | package | 0065-0419-28 | openfda.package_ndc |
| ndc | package | 0065-0419-18 | openfda.package_ndc |
| ndc | product | 0065-0419 | openfda.product_ndc |
| ndc11 | package | 00065041918 | derived:openfda.package_ndc |
| ndc11 | package | 00065041928 | derived:openfda.package_ndc |
| rxcui | 309714 | openfda.rxcui | |
| rxcui | 1088217 | openfda.rxcui | |
| spl id | 34aa9128-4bc4-45a6-aeae-a8c1f7699183 | id | |
| spl set id | e48d82f0-2f18-e514-4caa-e397d6713b99 | set_id | |
| unii | 7SA290YK68 | openfda.unii | |
| unii | RN3152OP35 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.