warnings
Warnings For use in the eyes only.
Lubricant Eye
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
- Lubricant Eye
- Generic name
- CARBOXYMETHYLCELLULOSE SODIUM 0.5%
- Manufacturer
- CARDINAL HEALTH 110, LLC. DBA LEADER
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 51a2d74f-5ff3-9921-e063-6294a90a345a
- SPL ID
- 5452bf0f-e978-fee9-e063-6294a90ae38b
- Version
- 2
- Effective date
- 2026-06-15
- Source export date
- 2026-10-27
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/b7a5e61d87a3b8f87f4c3ff7b526bfbf6baf84c840f565574c7d83d4083e2b38/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:49:46
| 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 | Lubricant Eye | openfda.brand_name | |
| generic name | CARBOXYMETHYLCELLULOSE SODIUM 0.5% | openfda.generic_name | |
| manufacturer name | CARDINAL HEALTH 110, LLC. DBA LEADER | openfda.manufacturer_name | |
| ndc | package | 70000-0751-2 | openfda.package_ndc |
| ndc | package | 70000-0751-1 | openfda.package_ndc |
| ndc | product | 70000-0751 | openfda.product_ndc |
| ndc11 | package | 70000075102 | derived:openfda.package_ndc |
| ndc11 | package | 70000075101 | derived:openfda.package_ndc |
| rxcui | 1188426 | openfda.rxcui | |
| spl id | 5452bf0f-e978-fee9-e063-6294a90ae38b | id | |
| spl set id | 51a2d74f-5ff3-9921-e063-6294a90a345a | set_id | |
| unii | K679OBS311 | 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.