Home FDA labels e58d9ebd-5f4b-42ca-b566-f137fc760d93 Liver Gallbladder HP 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 Liver Gallbladder HP
Generic name BELLADONNA, CARDUUS MARIANUS, CHELIDONIUM MAJUS, CHIONANTHUS VIRGINICA, CINCHONA OFFICINALIS, COLOCYNTHIS, LEPTANDRA VIRGINICA, LYCOPODIUM CLAVATUM, NATRUM SULPHURICUM, NUX VOMICA, PHOSPHORUS, PTELEA TRIFOLIATA, PULSATILLA (PRATENSIS), VERATRUM ALBUM
Manufacturer Energique, Inc.
Product type HUMAN OTC DRUG
SPL set ID 91f2500c-411f-4ef9-81f7-76e93d9bb3a5
SPL ID e58d9ebd-5f4b-42ca-b566-f137fc760d93
Version 2
Effective date 2026-04-02
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 02:29:03 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 · 22 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Liver Gallbladder HP openfda.brand_name generic name BELLADONNA, CARDUUS MARIANUS, CHELIDONIUM MAJUS, CHIONANTHUS VIRGINICA, CINCHONA OFFICINALIS, COLOCYNTHIS, LEPTANDRA VIRGINICA, LYCOPODIUM CLAVATUM, NATRUM SULPHURICUM, NUX VOMICA, PHOSPHORUS, PTELEA TRIFOLIATA, PULSATILLA (PRATENSIS), VERATRUM ALBUM openfda.generic_name manufacturer name Energique, Inc. openfda.manufacturer_name ndc package 44911-0679-1 openfda.package_ndc ndc product 44911-0679 openfda.product_ndc ndc11 package 44911067901 derived:openfda.package_ndc spl id e58d9ebd-5f4b-42ca-b566-f137fc760d93 id spl set id 91f2500c-411f-4ef9-81f7-76e93d9bb3a5 set_id unii 27YLU75U4W openfda.unii unii 7E889U5RNN openfda.unii unii 269XH13919 openfda.unii unii 5KQR6FTT0D openfda.unii unii 0YPR65R21J openfda.unii unii U946SH95EE openfda.unii unii M2O62YTN42 openfda.unii unii 8E272251DI openfda.unii unii S003A158SB openfda.unii unii WQZ3G9PF0H openfda.unii unii QNS6W5US1Z openfda.unii unii C88X29Y479 openfda.unii unii 23H32AOH17 openfda.unii unii S9Y4B22U2E 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 7 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.