Home FDA labels b52b8ee0-0a40-4ea4-8df5-a5a30f20c6fd 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 ARSENICUM ALBUM, CISTUS CANADENSIS, CLEMATIS ERECTA, COMOCLADIA DENTATA, CROTON TIGLIUM, DOLICHOS PRURIENS, GRAPHITES, IRIS VERSICOLOR, KALI BICHROMICUM, KALMIA LATIFOLIA, LACHESIS MUTUS, MERCURIUS SOLUBILIS, MEZEREUM, PRUNUS SPINOSA, RANUNCULUS BULBOSUS, RHUS TOX, ZINCUM PHOSPHORATUM
Manufacturer Deseret Biologicals, Inc.
Product type HUMAN OTC DRUG
SPL set ID 12a7c820-1e40-4024-9feb-fa657bd616cf
SPL ID b52b8ee0-0a40-4ea4-8df5-a5a30f20c6fd
Version 1
Effective date 2024-09-26
Source export date 2026-09-28
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/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:26:38 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 ARSENICUM ALBUM, CISTUS CANADENSIS, CLEMATIS ERECTA, COMOCLADIA DENTATA, CROTON TIGLIUM, DOLICHOS PRURIENS, GRAPHITES, IRIS VERSICOLOR, KALI BICHROMICUM, KALMIA LATIFOLIA, LACHESIS MUTUS, MERCURIUS SOLUBILIS, MEZEREUM, PRUNUS SPINOSA, RANUNCULUS BULBOSUS, RHUS TOX, ZINCUM PHOSPHORATUM openfda.generic_name manufacturer name Deseret Biologicals, Inc. openfda.manufacturer_name ndc package 43742-2204-1 openfda.package_ndc ndc product 43742-2204 openfda.product_ndc ndc11 package 43742220401 derived:openfda.package_ndc spl id b52b8ee0-0a40-4ea4-8df5-a5a30f20c6fd id spl set id 12a7c820-1e40-4024-9feb-fa657bd616cf set_id unii 3E271BSI0C openfda.unii unii X2N6E405GV openfda.unii unii VQQ72V371Q openfda.unii unii 324Y4038G2 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 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: If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. Tamper Evident: 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.