Rhus Toxicodendron
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
- Rhus Toxicodendron
- Generic name
- RHUS TOXICODENDRON
- Manufacturer
- Hahnemann Laboratories, INC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- f2a47b37-9848-0eac-e053-2995a90aadef
- SPL ID
- f2a47b37-9849-0eac-e053-2995a90aadef
- Version
- 1
- Effective date
- 2023-01-19
- Source export date
- 2026-09-28
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:49:39
| 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 | Rhus Toxicodendron | openfda.brand_name | |
| generic name | RHUS TOXICODENDRON | openfda.generic_name | |
| manufacturer name | Hahnemann Laboratories, INC. | openfda.manufacturer_name | |
| ndc | package | 37662-2426-4 | openfda.package_ndc |
| ndc | package | 37662-2422-1 | openfda.package_ndc |
| ndc | package | 37662-2429-1 | openfda.package_ndc |
| ndc | package | 37662-2424-1 | openfda.package_ndc |
| ndc | package | 37662-2427-1 | openfda.package_ndc |
| ndc | package | 37662-2422-3 | openfda.package_ndc |
| ndc | package | 37662-2426-1 | openfda.package_ndc |
| ndc | package | 37662-2425-3 | openfda.package_ndc |
| ndc | package | 37662-2423-2 | openfda.package_ndc |
| ndc | package | 37662-2428-4 | openfda.package_ndc |
| ndc | package | 37662-2423-1 | openfda.package_ndc |
| ndc | package | 37662-2425-4 | openfda.package_ndc |
| ndc | package | 37662-2425-1 | openfda.package_ndc |
| ndc | package | 37662-2424-4 | openfda.package_ndc |
| ndc | package | 37662-2427-4 | openfda.package_ndc |
| ndc | package | 37662-2427-3 | openfda.package_ndc |
| ndc | package | 37662-2423-3 | openfda.package_ndc |
| ndc | package | 37662-2427-2 | openfda.package_ndc |
| ndc | package | 37662-2426-2 | openfda.package_ndc |
| ndc | package | 37662-2426-3 | openfda.package_ndc |
| ndc | package | 37662-2428-3 | openfda.package_ndc |
| ndc | package | 37662-2425-2 | openfda.package_ndc |
| ndc | package | 37662-2424-2 | openfda.package_ndc |
| ndc | package | 37662-2428-1 | openfda.package_ndc |
| ndc | package | 37662-2428-2 | openfda.package_ndc |
| ndc | package | 37662-2422-2 | openfda.package_ndc |
| ndc | package | 37662-2424-3 | openfda.package_ndc |
| ndc | product | 37662-2423 | openfda.product_ndc |
| ndc | product | 37662-2424 | openfda.product_ndc |
| ndc | product | 37662-2422 | openfda.product_ndc |
| ndc | product | 37662-2425 | openfda.product_ndc |
| ndc | product | 37662-2429 | openfda.product_ndc |
| ndc | product | 37662-2427 | openfda.product_ndc |
| ndc | product | 37662-2426 | openfda.product_ndc |
| ndc | product | 37662-2428 | openfda.product_ndc |
| ndc11 | package | 37662242702 | derived:openfda.package_ndc |
| ndc11 | package | 37662242602 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.