warnings
Warnings For external use only
PATADAY ONCE DAILY RELIEF
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
- PATADAY ONCE DAILY RELIEF
- Generic name
- OLOPATADINE HYDROCHLORIDE
- Manufacturer
- Alcon Laboratories, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 6d07a5d6-265c-4735-97b3-8a2575b276cb
- SPL ID
- d735b7f6-185e-4fbb-a640-0f8aa8c57f45
- Version
- 5
- Effective date
- 2026-01-20
- 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 06:27:00
| 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 applno | NDA | 206276 | derived:openfda.application_number |
| application number | NDA206276 | openfda.application_number | |
| brand name | PATADAY ONCE DAILY RELIEF | openfda.brand_name | |
| generic name | OLOPATADINE HYDROCHLORIDE | openfda.generic_name | |
| manufacturer name | Alcon Laboratories, Inc. | openfda.manufacturer_name | |
| ndc | package | 0065-0816-12 | openfda.package_ndc |
| ndc | package | 0065-0816-04 | openfda.package_ndc |
| ndc | package | 0065-0816-01 | openfda.package_ndc |
| ndc | package | 0065-0816-02 | openfda.package_ndc |
| ndc | product | 0065-0816 | openfda.product_ndc |
| ndc11 | package | 00065081612 | derived:openfda.package_ndc |
| ndc11 | package | 00065081602 | derived:openfda.package_ndc |
| ndc11 | package | 00065081604 | derived:openfda.package_ndc |
| ndc11 | package | 00065081601 | derived:openfda.package_ndc |
| rxcui | 2474007 | openfda.rxcui | |
| rxcui | 1601086 | openfda.rxcui | |
| spl id | d735b7f6-185e-4fbb-a640-0f8aa8c57f45 | id | |
| spl set id | 6d07a5d6-265c-4735-97b3-8a2575b276cb | set_id | |
| unii | 2XG66W44KF | 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.