Home FDA labels 2d951add-0dae-5e36-e063-6394a90a1071 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 (canonical bytes are SHA-256 checked before publication)
Brand name Poison Ivy
Generic name XEROPHYLLUM ASPHODELOIDES, ACONITUM NAP., ANACARDIUM ORIENTALE, APIS MEL., BRYONIA, CANTHARIS, CROTON, GRAPHITES, GRINDELIA, MEZEREUM, NUX VOM., RANUNC. BULB., RHUS TOXICODENDRON, SARSAPARILLA, SULPHUR, ECHINACEA, RUMEX CRISP.,TARAXACUM, URTICA UR.
Manufacturer Newton Laboratories, Inc.
Product type HUMAN OTC DRUG
SPL set ID 9c9999b9-8d48-67f7-e053-2995a90aac96
SPL ID 2d951add-0dae-5e36-e063-6394a90a1071
Version 2
Effective date 2025-02-07
Source export date 2026-08-08
Source partition 10
Source file https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-08-08/13477f292fde418ab8b889dedaeed5fd633628cccdf0fe6d78a20f4b857aa1ee/drug-label-0010-of-0014.json.zip
Source manifest SHA-256 b39f3b00ad50d2e1b32aaf429248c6081e8799b35bce715b4fccb8cfa1ac4546
Import run 20260810T161303Z
Imported at 2026-08-10 17:34:17 Harmonized routes table 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.
Harmonized identifiers page 1 of 1 · 27 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Poison Ivy openfda.brand_name generic name XEROPHYLLUM ASPHODELOIDES, ACONITUM NAP., ANACARDIUM ORIENTALE, APIS MEL., BRYONIA, CANTHARIS, CROTON, GRAPHITES, GRINDELIA, MEZEREUM, NUX VOM., RANUNC. BULB., RHUS TOXICODENDRON, SARSAPARILLA, SULPHUR, ECHINACEA, RUMEX CRISP.,TARAXACUM, URTICA UR. openfda.generic_name manufacturer name Newton Laboratories, Inc. openfda.manufacturer_name ndc package 55714-2498-1 openfda.package_ndc ndc product 55714-2498 openfda.product_ndc ndc11 package 55714249801 derived:openfda.package_ndc spl id 2d951add-0dae-5e36-e063-6394a90a1071 id spl set id 9c9999b9-8d48-67f7-e053-2995a90aac96 set_id unii 269XH13919 openfda.unii unii X2N6E405GV openfda.unii unii 2H1576D5WG openfda.unii unii 4QQN74LH4O openfda.unii unii 39981FM375 openfda.unii unii 3Q034RO3BT openfda.unii unii 9N1RM2S62C openfda.unii unii IHN2NQ5OF9 openfda.unii unii 6IO182RP7A openfda.unii unii AEQ8NXJ0MB openfda.unii unii 4N9P6CC1DX openfda.unii unii T7J046YI2B openfda.unii unii 70FD1KFU70 openfda.unii unii U0NQ8555JD openfda.unii unii 0HK2GZK66E openfda.unii unii Y0F0BU8RDU openfda.unii unii 7S82P3R43Z openfda.unii unii IDB0NAZ6AI openfda.unii unii 9I4XB1GP2B openfda.unii
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 1 matching rows.
warnings WARNINGS SECTION WARNINGS: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding , ask a doctor before use.