warnings
STOP USE AND ASK DOCTOR If symptoms persist or recur, discontinue use. If pregnant or nursing, consult a licensed practitioner before using this product.
WHP Poison Ivy
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
- WHP Poison Ivy
- Generic name
- TOXICODENDRON PUBESCENS LEAF
- Manufacturer
- Washington Homeopathic Products
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 14a6f9af-2b61-002b-e063-6294a90a9c33
- SPL ID
- 47e3916e-c0fc-0d46-e063-6394a90a6283
- Version
- 2
- Effective date
- 2026-01-08
- Source export date
- 2026-09-28
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:38:39
| 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 | WHP Poison Ivy | openfda.brand_name | |
| generic name | TOXICODENDRON PUBESCENS LEAF | openfda.generic_name | |
| manufacturer name | Washington Homeopathic Products | openfda.manufacturer_name | |
| ndc | package | 71919-823-29 | openfda.package_ndc |
| ndc | package | 71919-823-14 | openfda.package_ndc |
| ndc | product | 71919-823 | openfda.product_ndc |
| ndc11 | package | 71919082314 | derived:openfda.package_ndc |
| ndc11 | package | 71919082329 | derived:openfda.package_ndc |
| spl id | 47e3916e-c0fc-0d46-e063-6394a90a6283 | id | |
| spl set id | 14a6f9af-2b61-002b-e063-6294a90a9c33 | set_id | |
| unii | 6IO182RP7A | 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.