warnings
Warnings
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 HYDROCHLORIDE
- Manufacturer
- BETTER LIVING BRANDS, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- eb60ae7d-87db-7413-e053-2a95a90afd76
- SPL ID
- 38a06b8a-bd81-4696-e063-6294a90a1f38
- Version
- 6
- Effective date
- 2025-06-28
- Source export date
- 2026-09-28
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:04:55
| 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 | 078933 | derived:openfda.application_number |
| application number | ANDA078933 | openfda.application_number | |
| brand name | Allergy Relief | openfda.brand_name | |
| generic name | CETIRIZINE HYDROCHLORIDE | openfda.generic_name | |
| manufacturer name | BETTER LIVING BRANDS, LLC | openfda.manufacturer_name | |
| ndc | package | 21130-712-12 | openfda.package_ndc |
| ndc | package | 21130-712-81 | openfda.package_ndc |
| ndc | package | 21130-712-46 | openfda.package_ndc |
| ndc | package | 21130-712-09 | openfda.package_ndc |
| ndc | package | 21130-712-03 | openfda.package_ndc |
| ndc | package | 21130-712-58 | openfda.package_ndc |
| ndc | product | 21130-712 | openfda.product_ndc |
| ndc11 | package | 21130071258 | derived:openfda.package_ndc |
| ndc11 | package | 21130071246 | derived:openfda.package_ndc |
| ndc11 | package | 21130071209 | derived:openfda.package_ndc |
| ndc11 | package | 21130071203 | derived:openfda.package_ndc |
| ndc11 | package | 21130071281 | derived:openfda.package_ndc |
| ndc11 | package | 21130071212 | derived:openfda.package_ndc |
| rxcui | 1014678 | openfda.rxcui | |
| spl id | 38a06b8a-bd81-4696-e063-6294a90a1f38 | id | |
| spl set id | eb60ae7d-87db-7413-e053-2a95a90afd76 | 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.