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
- 1c7d2342-ba1c-4244-9814-d92a05725d4e
- SPL ID
- 7f324d32-7a86-4976-b0f4-b80283e5fc29
- Version
- 7
- Effective date
- 2026-01-20
- Source export date
- 2026-10-12
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:25:10
| 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 | 021545 | derived:openfda.application_number |
| application number | NDA021545 | 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 | 0065-8150-04 | openfda.package_ndc |
| ndc | package | 0065-8150-01 | openfda.package_ndc |
| ndc | package | 0065-8150-07 | openfda.package_ndc |
| ndc | package | 0065-8150-03 | openfda.package_ndc |
| ndc | product | 0065-8150 | openfda.product_ndc |
| ndc11 | package | 00065815003 | derived:openfda.package_ndc |
| ndc11 | package | 00065815007 | derived:openfda.package_ndc |
| ndc11 | package | 00065815001 | derived:openfda.package_ndc |
| ndc11 | package | 00065815004 | derived:openfda.package_ndc |
| rxcui | 1111343 | openfda.rxcui | |
| rxcui | 1111345 | openfda.rxcui | |
| spl id | 7f324d32-7a86-4976-b0f4-b80283e5fc29 | id | |
| spl set id | 1c7d2342-ba1c-4244-9814-d92a05725d4e | 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.