warnings
Warnings Do not use to treat food allergies. Stop use and ask a doctor if symptoms persist for more than 7 days or worsen. If pregnant or breastfeeding ask a health professional before use. Keep out of reach of children.
Seasonal 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
- Seasonal Allergy Relief
- Generic name
- ONION, SODIUM CHLORIDE, HISTAMINE DIHYDROCHLORIDE, CUCUMBER, GALPHIMIA GLAUCA FLOWERING TOP, AND STRYCHNOS NUX-VOMICA SEED
- Manufacturer
- Hyland's Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 101e6b80-cdae-49e5-acfb-f056448856ec
- SPL ID
- 340a9e19-c1ce-1fa8-e063-6394a90aebf6
- Version
- 9
- Effective date
- 2025-04-30
- Source export date
- 2026-09-28
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:19:31
| 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 | Seasonal Allergy Relief | openfda.brand_name | |
| generic name | ONION, SODIUM CHLORIDE, HISTAMINE DIHYDROCHLORIDE, CUCUMBER, GALPHIMIA GLAUCA FLOWERING TOP, AND STRYCHNOS NUX-VOMICA SEED | openfda.generic_name | |
| manufacturer name | Hyland's Inc. | openfda.manufacturer_name | |
| ndc | package | 54973-3012-1 | openfda.package_ndc |
| ndc | package | 54973-3012-2 | openfda.package_ndc |
| ndc | product | 54973-3012 | openfda.product_ndc |
| ndc11 | package | 54973301202 | derived:openfda.package_ndc |
| ndc11 | package | 54973301201 | derived:openfda.package_ndc |
| spl id | 340a9e19-c1ce-1fa8-e063-6394a90aebf6 | id | |
| spl set id | 101e6b80-cdae-49e5-acfb-f056448856ec | set_id | |
| unii | 269XH13919 | openfda.unii | |
| unii | 3POA0Q644U | openfda.unii | |
| unii | 93PH5Q8M7E | openfda.unii | |
| unii | YY7C30VXJT | openfda.unii | |
| unii | 451W47IQ8X | openfda.unii | |
| unii | 492225Q21H | 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.