warnings
Ask a doctor before use if you have a fever.
SINUSCALM ALLERGY
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
- SINUSCALM ALLERGY
- Generic name
- ATROPA BELLADONNA. SPIGELIA ANTHELMIA. SANGUINARIA CANADENSIS ROOT
- Manufacturer
- Boiron
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 4d3f554a-c8b2-3121-e063-6394a90a1598
- SPL ID
- 4d3f554a-c8b3-3121-e063-6394a90a1598
- Version
- 1
- Effective date
- 2026-03-17
- Source export date
- 2026-09-28
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:55:17
| 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 | SINUSCALM ALLERGY | openfda.brand_name | |
| generic name | ATROPA BELLADONNA. SPIGELIA ANTHELMIA. SANGUINARIA CANADENSIS ROOT | openfda.generic_name | |
| manufacturer name | Boiron | openfda.manufacturer_name | |
| ndc | package | 0220-9286-04 | openfda.package_ndc |
| ndc | product | 0220-9286 | openfda.product_ndc |
| ndc11 | package | 00220928604 | derived:openfda.package_ndc |
| spl id | 4d3f554a-c8b3-3121-e063-6394a90a1598 | id | |
| spl set id | 4d3f554a-c8b2-3121-e063-6394a90a1598 | set_id | |
| unii | WYT05213GE | openfda.unii | |
| unii | WQZ3G9PF0H | openfda.unii | |
| unii | N9288CD508 | 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.