Digitalis Purpurea
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
- Digitalis Purpurea
- Generic name
- DIGITALIS PURPUREA
- Manufacturer
- Hahnemann Laboratories, INC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- e3a004d3-f770-e4e9-e053-2995a90ab43c
- SPL ID
- e3a004d3-f771-e4e9-e053-2995a90ab43c
- Version
- 1
- Effective date
- 2022-07-12
- Source export date
- 2026-10-27
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/a73bb3b6a943796a18cd4bcd0917240b579be4636d00e6e39481bafbd8093f69/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:32:45
| 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 | Digitalis Purpurea | openfda.brand_name | |
| generic name | DIGITALIS PURPUREA | openfda.generic_name | |
| manufacturer name | Hahnemann Laboratories, INC. | openfda.manufacturer_name | |
| ndc | package | 37662-0820-3 | openfda.package_ndc |
| ndc | package | 37662-0817-2 | openfda.package_ndc |
| ndc | package | 37662-0823-3 | openfda.package_ndc |
| ndc | package | 37662-0823-1 | openfda.package_ndc |
| ndc | package | 37662-0822-1 | openfda.package_ndc |
| ndc | package | 37662-0824-1 | openfda.package_ndc |
| ndc | package | 37662-0821-4 | openfda.package_ndc |
| ndc | package | 37662-0820-4 | openfda.package_ndc |
| ndc | package | 37662-0823-2 | openfda.package_ndc |
| ndc | package | 37662-0818-3 | openfda.package_ndc |
| ndc | package | 37662-0817-3 | openfda.package_ndc |
| ndc | package | 37662-0818-4 | openfda.package_ndc |
| ndc | package | 37662-0820-1 | openfda.package_ndc |
| ndc | package | 37662-0816-2 | openfda.package_ndc |
| ndc | package | 37662-0820-2 | openfda.package_ndc |
| ndc | package | 37662-0816-3 | openfda.package_ndc |
| ndc | package | 37662-0819-1 | openfda.package_ndc |
| ndc | package | 37662-0822-2 | openfda.package_ndc |
| ndc | package | 37662-0821-1 | openfda.package_ndc |
| ndc | package | 37662-0822-4 | openfda.package_ndc |
| ndc | package | 37662-0817-1 | openfda.package_ndc |
| ndc | package | 37662-0821-2 | openfda.package_ndc |
| ndc | package | 37662-0819-2 | openfda.package_ndc |
| ndc | package | 37662-0819-3 | openfda.package_ndc |
| ndc | package | 37662-0818-1 | openfda.package_ndc |
| ndc | package | 37662-0822-3 | openfda.package_ndc |
| ndc | package | 37662-0823-4 | openfda.package_ndc |
| ndc | package | 37662-0821-3 | openfda.package_ndc |
| ndc | package | 37662-0816-1 | openfda.package_ndc |
| ndc | package | 37662-0819-4 | openfda.package_ndc |
| ndc | package | 37662-0818-2 | openfda.package_ndc |
| ndc | product | 37662-0817 | openfda.product_ndc |
| ndc | product | 37662-0824 | openfda.product_ndc |
| ndc | product | 37662-0819 | openfda.product_ndc |
| ndc | product | 37662-0823 | openfda.product_ndc |
| ndc | product | 37662-0822 | openfda.product_ndc |
| ndc | product | 37662-0820 | openfda.product_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.