Home FDA labels ab5ed0cd-3325-4b6f-bd9b-0f2acca5893f Hepapar 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 Hepapar
Generic name CARDUUS MARIANUS, CHELIDONIUM MAJUS, LAPPA MAJOR, TARAXACUM OFFICINALE, BOLDO, CHOLINUM, HEPAR SUIS, LYCOPODIUM CLAVATUM, MERCURIUS SOLUBILIS, NATRUM SULPHURICUM, NUX VOMICA, PHOSPHORUS, QUERCUS GLANDIUM SPIRITUS, AURUM MURIATICUM NATRONATUM, CHENOPODIUM ANTHELMINTICUM
Manufacturer Energique, Inc.
Product type HUMAN OTC DRUG
SPL set ID ddbcbad9-ddb0-4ffd-a769-4de02e669845
SPL ID ab5ed0cd-3325-4b6f-bd9b-0f2acca5893f
Version 2
Effective date 2026-05-19
Source export date 2026-10-12
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/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:29:02 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 · 23 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Hepapar openfda.brand_name generic name CARDUUS MARIANUS, CHELIDONIUM MAJUS, LAPPA MAJOR, TARAXACUM OFFICINALE, BOLDO, CHOLINUM, HEPAR SUIS, LYCOPODIUM CLAVATUM, MERCURIUS SOLUBILIS, NATRUM SULPHURICUM, NUX VOMICA, PHOSPHORUS, QUERCUS GLANDIUM SPIRITUS, AURUM MURIATICUM NATRONATUM, CHENOPODIUM ANTHELMINTICUM openfda.generic_name manufacturer name Energique, Inc. openfda.manufacturer_name ndc package 44911-0719-1 openfda.package_ndc ndc product 44911-0719 openfda.product_ndc ndc11 package 44911071901 derived:openfda.package_ndc spl id ab5ed0cd-3325-4b6f-bd9b-0f2acca5893f id spl set id ddbcbad9-ddb0-4ffd-a769-4de02e669845 set_id unii 27YLU75U4W openfda.unii unii 7E889U5RNN openfda.unii unii 269XH13919 openfda.unii unii 324Y4038G2 openfda.unii unii 0YPR65R21J openfda.unii unii 39981FM375 openfda.unii unii U946SH95EE openfda.unii unii 4H5RSU087I openfda.unii unii 7THJ3EG9SY openfda.unii unii Q4EWM09M3O openfda.unii unii Q7MU1F4GLY openfda.unii unii 7FT6QUT299 openfda.unii unii 6EC706HI7F openfda.unii unii C88X29Y479 openfda.unii unii 597E9BI3Z3 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: Stop use and ask a doctor if symptoms persist for more than 2 days. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. DO NOT USE IF TAMPER EVIDENT SEAL IS BROKEN OR MISSING Store in a cool, dry place.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.