warnings
STOP USE AND ASK DOCTOR If symptoms persist/worsen or if pregnant/nursing, stop use and consult your practitioner.
Bellis Perennis Kit Refill
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
- Bellis Perennis Kit Refill
- Generic name
- BELLIS PERENNIS
- Manufacturer
- Washington Homeopathic Products
- Product type
- HUMAN OTC DRUG
- SPL set ID
- e11a653d-42d4-1b82-e053-2a95a90a3b58
- SPL ID
- 2cc7e78c-a576-f042-e063-6394a90ad14c
- Version
- 4
- Effective date
- 2025-01-28
- Source export date
- 2026-10-12
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:41:41
| 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 | Bellis Perennis Kit Refill | openfda.brand_name | |
| generic name | BELLIS PERENNIS | openfda.generic_name | |
| manufacturer name | Washington Homeopathic Products | openfda.manufacturer_name | |
| ndc | package | 71919-773-01 | openfda.package_ndc |
| ndc | product | 71919-773 | openfda.product_ndc |
| ndc11 | package | 71919077301 | derived:openfda.package_ndc |
| spl id | 2cc7e78c-a576-f042-e063-6394a90ad14c | id | |
| spl set id | e11a653d-42d4-1b82-e053-2a95a90a3b58 | set_id | |
| unii | 2HU33I03UY | 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.