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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
- Allergy Relief
- Generic name
- CETIRIZINE HCL
- Manufacturer
- WALMART INC. (see also Equate)
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 967be504-85b1-4e9b-9b08-2b27a43fa0aa
- SPL ID
- f14d4109-2aa6-4709-a64e-efb3ac5ffe7e
- Version
- 3
- Effective date
- 2026-06-18
- Source export date
- 2026-09-28
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:36:38
| 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 | Allergy Relief | openfda.brand_name | |
| generic name | CETIRIZINE HCL | openfda.generic_name | |
| manufacturer name | WALMART INC. (see also Equate) | openfda.manufacturer_name | |
| ndc | package | 79903-347-25 | openfda.package_ndc |
| ndc | product | 79903-347 | openfda.product_ndc |
| ndc11 | package | 79903034725 | derived:openfda.package_ndc |
| rxcui | 1014675 | openfda.rxcui | |
| spl id | f14d4109-2aa6-4709-a64e-efb3ac5ffe7e | id | |
| spl set id | 967be504-85b1-4e9b-9b08-2b27a43fa0aa | 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.