warnings
WARNINGS Stop use and ask a physician if symptoms persist for more than 3 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 |
|---|
| SUBLINGUAL |
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 | Ledum Palustre 200ck | openfda.brand_name | |
| generic name | LEDUM PALUSTRE | openfda.generic_name | |
| manufacturer name | SEVENE USA | openfda.manufacturer_name | |
| ndc | package | 76472-3023-1 | openfda.package_ndc |
| ndc | product | 76472-3023 | openfda.product_ndc |
| ndc11 | package | 76472302301 | derived:openfda.package_ndc |
| spl id | 2ddc5714-317a-0005-e063-6394a90af292 | id | |
| spl set id | cf859336-f6ae-349c-e053-2995a90a27ef | set_id | |
| unii | 877L01IZ0P | 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.