AllergyCalm
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
- AllergyCalm
- Generic name
- ONION, AMBROSIA ARTEMISIIFOLIA, EUPHRASIA STRICTA, HISTAMINE DIHYDROCHLORIDE, SCHOENOCAULON OFFICINALE SEED, SOLIDAGO VIRGAUREA FLOWERING TOP
- Manufacturer
- Boiron
- Product type
- HUMAN OTC DRUG
- SPL set ID
- d92d9269-7532-2f0e-e053-2a95a90ab0d6
- SPL ID
- 38e22593-4061-ae63-e063-6294a90a3d39
- Version
- 7
- Effective date
- 2025-07-01
- Source export date
- 2026-11-06
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/5ab46f90f6b44e2aa9affb3cb9a1420d82b92a8f942c23fe463364760a659d66/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
- Import run
- 20261106T075659Z
- Imported at
- 2026-11-06 08:08:47
| 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 | AllergyCalm | openfda.brand_name | |
| generic name | ONION, AMBROSIA ARTEMISIIFOLIA, EUPHRASIA STRICTA, HISTAMINE DIHYDROCHLORIDE, SCHOENOCAULON OFFICINALE SEED, SOLIDAGO VIRGAUREA FLOWERING TOP | openfda.generic_name | |
| manufacturer name | Boiron | openfda.manufacturer_name | |
| ndc | package | 0220-9306-29 | openfda.package_ndc |
| ndc | package | 0220-9306-91 | openfda.package_ndc |
| ndc | package | 0220-9306-92 | openfda.package_ndc |
| ndc | package | 0220-9306-04 | openfda.package_ndc |
| ndc | product | 0220-9306 | openfda.product_ndc |
| ndc11 | package | 00220930691 | derived:openfda.package_ndc |
| ndc11 | package | 00220930604 | derived:openfda.package_ndc |
| ndc11 | package | 00220930692 | derived:openfda.package_ndc |
| ndc11 | package | 00220930629 | derived:openfda.package_ndc |
| spl id | 38e22593-4061-ae63-e063-6294a90a3d39 | id | |
| spl set id | d92d9269-7532-2f0e-e053-2a95a90ab0d6 | set_id | |
| unii | C9642I91WL | openfda.unii | |
| unii | 3POA0Q644U | openfda.unii | |
| unii | 9W34L2CQ9A | openfda.unii | |
| unii | 6NAF1689IO | openfda.unii | |
| unii | 492225Q21H | openfda.unii | |
| unii | 5405K23S50 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.