Home FDA labels 98b2924a-55cb-42d8-ad52-3bc7b4b13add Herz Plus 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 Herz Plus
Generic name CISTUS CANADENSIS, CLEMATIS ERECTA, CROTON TIGLIUM, DOLICHOS PRURIENS, IRIS VERSICOLOR, PRUNUS SPINOSA, RANUNCULUS BULBOSUS, KALI BICHROMICUM, ZINCUM PHOSPHORATUM, ARSENICUM ALBUM, COMOCLADIA DENTATA, GRAPHITES, KALMIA LATIFOLIA, LACHESIS MUTUS, MEZEREUM, RHUS TOX, THALLIUM METALLICUM
Manufacturer Deseret Biologicals, Inc.
Product type HUMAN OTC DRUG
SPL set ID aa893170-df1b-4490-ae33-8ef3160c9c1d
SPL ID 98b2924a-55cb-42d8-ad52-3bc7b4b13add
Version 5
Effective date 2024-09-11
Source export date 2026-10-12
Source partition 4
Source file https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 01:39:33 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 · 25 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Herz Plus openfda.brand_name generic name CISTUS CANADENSIS, CLEMATIS ERECTA, CROTON TIGLIUM, DOLICHOS PRURIENS, IRIS VERSICOLOR, PRUNUS SPINOSA, RANUNCULUS BULBOSUS, KALI BICHROMICUM, ZINCUM PHOSPHORATUM, ARSENICUM ALBUM, COMOCLADIA DENTATA, GRAPHITES, KALMIA LATIFOLIA, LACHESIS MUTUS, MEZEREUM, RHUS TOX, THALLIUM METALLICUM openfda.generic_name manufacturer name Deseret Biologicals, Inc. openfda.manufacturer_name ndc package 43742-1890-1 openfda.package_ndc ndc product 43742-1890 openfda.product_ndc ndc11 package 43742189001 derived:openfda.package_ndc spl id 98b2924a-55cb-42d8-ad52-3bc7b4b13add id spl set id aa893170-df1b-4490-ae33-8ef3160c9c1d set_id unii 3E271BSI0C openfda.unii unii X2N6E405GV openfda.unii unii VQQ72V371Q openfda.unii unii 813396S1PC openfda.unii unii 4QQN74LH4O openfda.unii unii 79N6542N18 openfda.unii unii 46G3W789Q3 openfda.unii unii 53Y84VPS2W openfda.unii unii 6IO182RP7A openfda.unii unii S7V92P67HO openfda.unii unii AEQ8NXJ0MB openfda.unii unii AD84R52XLF openfda.unii unii VSW71SS07I openfda.unii unii T4423S18FM openfda.unii unii 0HK2GZK66E openfda.unii unii X43D4L3DQC openfda.unii unii 396421SP9F 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: Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use. Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.