warnings
WARNINGS
Fexofenadine HCL
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
- Fexofenadine HCL
- Generic name
- FEXOFENADINE HCL
- Manufacturer
- Bryant Ranch Prepack
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 6bc92969-0d06-4bf5-a634-80964464546c
- SPL ID
- 7921f011-b1c5-4bf9-977c-dea10b285be0
- Version
- 2
- Effective date
- 2024-08-23
- Source export date
- 2026-10-12
- Source partition
- 5
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:44:00
| 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 | 204097 | derived:openfda.application_number |
| application number | ANDA204097 | openfda.application_number | |
| brand name | Fexofenadine HCL | openfda.brand_name | |
| generic name | FEXOFENADINE HCL | openfda.generic_name | |
| manufacturer name | Bryant Ranch Prepack | openfda.manufacturer_name | |
| ndc | package | 71335-1217-1 | openfda.package_ndc |
| ndc | package | 71335-1217-5 | openfda.package_ndc |
| ndc | package | 71335-1217-3 | openfda.package_ndc |
| ndc | package | 71335-1217-2 | openfda.package_ndc |
| ndc | package | 71335-1217-4 | openfda.package_ndc |
| ndc | package | 71335-1217-6 | openfda.package_ndc |
| ndc | package | 71335-1217-7 | openfda.package_ndc |
| ndc | product | 71335-1217 | openfda.product_ndc |
| ndc11 | package | 71335121706 | derived:openfda.package_ndc |
| ndc11 | package | 71335121702 | derived:openfda.package_ndc |
| ndc11 | package | 71335121701 | derived:openfda.package_ndc |
| ndc11 | package | 71335121707 | derived:openfda.package_ndc |
| ndc11 | package | 71335121703 | derived:openfda.package_ndc |
| ndc11 | package | 71335121705 | derived:openfda.package_ndc |
| ndc11 | package | 71335121704 | derived:openfda.package_ndc |
| rxcui | 997420 | openfda.rxcui | |
| spl id | 7921f011-b1c5-4bf9-977c-dea10b285be0 | id | |
| spl set id | 6bc92969-0d06-4bf5-a634-80964464546c | set_id | |
| unii | 2S068B75ZU | 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.