warnings
Warnings Stop use and ask a doctor if symptoms persist for more than 3 days or worsen. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children.
Genexa Allergy Care
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
- Genexa Allergy Care
- Generic name
- ALLIUM CEPA, AMBROSIA ARTEMISIIFOLIA, ARUNDO MAURITANICA, DULCAMARA, EUPHRASIA OFFICINALIS, NUX VOMICA, PULSATILLA, RANUNCULUS BULBOSUS, SABADILLA, SINAPIS NIGRA, STICTA PULMONARIA, WYETHIA HELENOIDES
- Manufacturer
- Genexa Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- b5fddd8f-a380-6e88-e053-2a95a90a6b89
- SPL ID
- 59af45df-ac36-9901-e063-6294a90a71aa
- Version
- 11
- Effective date
- 2026-08-22
- 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 05:37:42
| 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 |
|---|---|---|---|
| brand name | Genexa Allergy Care | openfda.brand_name | |
| generic name | ALLIUM CEPA, AMBROSIA ARTEMISIIFOLIA, ARUNDO MAURITANICA, DULCAMARA, EUPHRASIA OFFICINALIS, NUX VOMICA, PULSATILLA, RANUNCULUS BULBOSUS, SABADILLA, SINAPIS NIGRA, STICTA PULMONARIA, WYETHIA HELENOIDES | openfda.generic_name | |
| manufacturer name | Genexa Inc. | openfda.manufacturer_name | |
| ndc | package | 69676-0052-3 | openfda.package_ndc |
| ndc | package | 69676-0052-1 | openfda.package_ndc |
| ndc | product | 69676-0052 | openfda.product_ndc |
| ndc11 | package | 69676005201 | derived:openfda.package_ndc |
| ndc11 | package | 69676005203 | derived:openfda.package_ndc |
| spl id | 59af45df-ac36-9901-e063-6294a90a71aa | id | |
| spl set id | b5fddd8f-a380-6e88-e053-2a95a90a6b89 | set_id | |
| unii | C9642I91WL | openfda.unii | |
| unii | 269XH13919 | openfda.unii | |
| unii | 8P2VLG2456 | openfda.unii | |
| unii | KPS1B1162N | openfda.unii | |
| unii | J10PD1AQ0N | openfda.unii | |
| unii | 9W34L2CQ9A | openfda.unii | |
| unii | 8LTY55LQ8D | openfda.unii | |
| unii | AEQ8NXJ0MB | openfda.unii | |
| unii | 6NAF1689IO | openfda.unii | |
| unii | 8E272251DI | openfda.unii | |
| unii | ZXE7LB03WC | openfda.unii | |
| unii | D1YM0P5Z2T | 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.