warnings
For external use only Avoid contact with eyes. If swallowed, get medical help or contact a Poison Control Center right away.
Calendula
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
- Calendula
- Generic name
- CALENDULA OFFICINALIS FLOWERING TOP
- Manufacturer
- Laboratoires Boiron
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 25764f5a-378b-4103-81a1-2a6309e3e8e1
- SPL ID
- f706dc04-987c-ee0d-e053-6394a90a3629
- Version
- 7
- Effective date
- 2023-03-16
- Source export date
- 2026-09-28
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:12:47
| Harmonized routes |
|---|
| TOPICAL |
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 | Calendula | openfda.brand_name | |
| generic name | CALENDULA OFFICINALIS FLOWERING TOP | openfda.generic_name | |
| manufacturer name | Laboratoires Boiron | openfda.manufacturer_name | |
| ndc | package | 0220-1108-59 | openfda.package_ndc |
| ndc | product | 0220-1108 | openfda.product_ndc |
| ndc11 | package | 00220110859 | derived:openfda.package_ndc |
| spl id | f706dc04-987c-ee0d-e053-6394a90a3629 | id | |
| spl set id | 25764f5a-378b-4103-81a1-2a6309e3e8e1 | set_id | |
| unii | 18E7415PXQ | 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.