warnings
Warnings For external use only
Carboxymethylcellulose Sodium Eye Drops 0.5%
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
- Carboxymethylcellulose Sodium Eye Drops 0.5%
- Generic name
- CARBOXYMETHYLCELLULOSE SODIUM EYE DROPS 0.5%
- Manufacturer
- Aurolab
- Product type
- HUMAN OTC DRUG
- SPL set ID
- e8b4df3b-3d81-b3ca-e053-2a95a90af2ec
- SPL ID
- 495c072a-fa45-45a7-e063-6394a90ad7d6
- Version
- 9
- Effective date
- 2026-01-27
- Source export date
- 2026-09-28
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:27:01
| Harmonized routes |
|---|
| TOPICAL |
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 | Carboxymethylcellulose Sodium Eye Drops 0.5% | openfda.brand_name | |
| generic name | CARBOXYMETHYLCELLULOSE SODIUM EYE DROPS 0.5% | openfda.generic_name | |
| manufacturer name | Aurolab | openfda.manufacturer_name | |
| ndc | package | 16030-501-05 | openfda.package_ndc |
| ndc | product | 16030-501 | openfda.product_ndc |
| ndc11 | package | 16030050105 | derived:openfda.package_ndc |
| rxcui | 1188426 | openfda.rxcui | |
| spl id | 495c072a-fa45-45a7-e063-6394a90ad7d6 | id | |
| spl set id | e8b4df3b-3d81-b3ca-e053-2a95a90af2ec | 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.