warnings
Warning
All Day Allergy 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
- All Day Allergy Relief
- Generic name
- CETIRIZINE HCL
- Manufacturer
- P & L Development, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 7dabf6bd-8a96-4e7f-bc19-5a47cec36419
- SPL ID
- 58589d4e-ad27-423d-a703-3d3e5eb82377
- Version
- 6
- Effective date
- 2025-05-16
- Source export date
- 2026-10-12
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:56:33
| Harmonized routes |
|---|
| ORAL |
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 | ANDA | 213105 | derived:openfda.application_number |
| application number | ANDA213105 | openfda.application_number | |
| brand name | All Day Allergy Relief | openfda.brand_name | |
| generic name | CETIRIZINE HCL | openfda.generic_name | |
| manufacturer name | P & L Development, LLC | openfda.manufacturer_name | |
| ndc | package | 59726-064-12 | openfda.package_ndc |
| ndc | product | 59726-064 | openfda.product_ndc |
| ndc11 | package | 59726006412 | derived:openfda.package_ndc |
| rxcui | 1014675 | openfda.rxcui | |
| spl id | 58589d4e-ad27-423d-a703-3d3e5eb82377 | id | |
| spl set id | 7dabf6bd-8a96-4e7f-bc19-5a47cec36419 | set_id | |
| unii | 64O047KTOA | 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.