warnings
STOP USE AND ASK DOCTOR If symptoms persist/worsen or if pregnant/nursing, stop use and consult your practitioner.
Berberis Vulgaris 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
- Berberis Vulgaris Kit Refill
- Generic name
- BERBERIS VULGARIS ROOT BARK
- Manufacturer
- Washington Homeopathic Products
- Product type
- HUMAN OTC DRUG
- SPL set ID
- deab1d3e-75a1-480e-e053-2995a90a0a75
- SPL ID
- 2cc7e49e-b394-f002-e063-6394a90a15de
- Version
- 4
- Effective date
- 2025-01-28
- 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 05:14:26
| 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 | Berberis Vulgaris Kit Refill | openfda.brand_name | |
| generic name | BERBERIS VULGARIS ROOT BARK | openfda.generic_name | |
| manufacturer name | Washington Homeopathic Products | openfda.manufacturer_name | |
| ndc | package | 71919-762-01 | openfda.package_ndc |
| ndc | product | 71919-762 | openfda.product_ndc |
| ndc11 | package | 71919076201 | derived:openfda.package_ndc |
| spl id | 2cc7e49e-b394-f002-e063-6394a90a15de | id | |
| spl set id | deab1d3e-75a1-480e-e053-2995a90a0a75 | set_id | |
| unii | 1TH8Q20J0U | 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.