warnings
Warnings: Consult your health care provider if symptoms persist more than 5 days or worsen.
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
| Harmonized routes |
|---|
| ORAL |
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 | Pulsatilla | openfda.brand_name | |
| generic name | PULSATILLA | openfda.generic_name | |
| manufacturer name | True Botanica, LLC | openfda.manufacturer_name | |
| ndc | package | 53645-1980-2 | openfda.package_ndc |
| ndc | product | 53645-1980 | openfda.product_ndc |
| ndc11 | package | 53645198002 | derived:openfda.package_ndc |
| spl id | fe1b3122-b69c-46fa-e053-6394a90afd59 | id | |
| spl set id | 61975b02-4357-e6b8-e053-2991aa0a42a3 | set_id | |
| unii | I76KB35JEV | openfda.unii |
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Adverse event summaries are temporarily unavailable. Other product information remains available.