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All Day Allergy
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
- Generic name
- CETIRIZINE HCL
- Manufacturer
- WALMART INC. (see also Equate)
- Product type
- HUMAN OTC DRUG
- SPL set ID
- c8016d34-aa72-4857-b5ed-5476948b386a
- SPL ID
- b8b7fc7d-e7c1-4a7c-8d10-83d4bb696bf3
- Version
- 4
- Effective date
- 2026-02-20
- Source export date
- 2026-09-28
- 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/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:17:23
| 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 | openfda.brand_name | |
| generic name | CETIRIZINE HCL | openfda.generic_name | |
| manufacturer name | WALMART INC. (see also Equate) | openfda.manufacturer_name | |
| ndc | package | 79903-084-25 | openfda.package_ndc |
| ndc | product | 79903-084 | openfda.product_ndc |
| ndc11 | package | 79903008425 | derived:openfda.package_ndc |
| rxcui | 1014675 | openfda.rxcui | |
| spl id | b8b7fc7d-e7c1-4a7c-8d10-83d4bb696bf3 | id | |
| spl set id | c8016d34-aa72-4857-b5ed-5476948b386a | 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.