Home FDA labels c7c0766c-5fa4-95e0-e053-2995a90ac48f HFE 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 HFE
Generic name APIS MELLIFICA, BELLADONNA, CAULOPHYLLUM THALICTROIDES, CIMICIFUGA RACEMOSA, DIOSCOREA VILLOSA, GELSEMIUM SEMPERVIRENS, HELONIAS DIOICA, MAGNESIA PHOSPHORICA, ORYCTOLAGUS CUNICULUS (RABBIT) ADRENAL GLAND, ORYCTOLAGUS CUNICULUS (RABBIT) OVARY, ORYCTOLAGUS CUNICULUS (RABBIT) UTERUS, VIBURNUM OPULUS
Manufacturer Seroyal USA
Product type HUMAN OTC DRUG
SPL set ID 7d508fdd-ba8b-07ec-e053-2991aa0a29ef
SPL ID c7c0766c-5fa4-95e0-e053-2995a90ac48f
Version 3
Effective date 2021-07-22
Source export date 2026-11-06
Source partition 3
Source file https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-11-06/97001096994db9ca8cee114e6c3bb5298d3c573158ffc1ab8692d82e76a3eb40/drug-label-0003-of-0014.json.zip
Source manifest SHA-256 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run 20261108T063105Z
Imported at 2026-11-08 06:56:03 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 · 20 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name HFE openfda.brand_name generic name APIS MELLIFICA, BELLADONNA, CAULOPHYLLUM THALICTROIDES, CIMICIFUGA RACEMOSA, DIOSCOREA VILLOSA, GELSEMIUM SEMPERVIRENS, HELONIAS DIOICA, MAGNESIA PHOSPHORICA, ORYCTOLAGUS CUNICULUS (RABBIT) ADRENAL GLAND, ORYCTOLAGUS CUNICULUS (RABBIT) OVARY, ORYCTOLAGUS CUNICULUS (RABBIT) UTERUS, VIBURNUM OPULUS openfda.generic_name manufacturer name Seroyal USA openfda.manufacturer_name ndc package 62106-0623-0 openfda.package_ndc ndc product 62106-0623 openfda.product_ndc ndc11 package 62106062300 derived:openfda.package_ndc spl id c7c0766c-5fa4-95e0-e053-2995a90ac48f id spl set id 7d508fdd-ba8b-07ec-e053-2991aa0a29ef set_id unii IWY3IWX2G8 openfda.unii unii QGY289M89Q openfda.unii unii T1UG6H6805 openfda.unii unii NQX84Z32G6 openfda.unii unii JTJ6HH6YEH openfda.unii unii 639KR60Q1Q openfda.unii unii HF539G9L3Q openfda.unii unii WQZ3G9PF0H openfda.unii unii XA09528U2R openfda.unii unii 7S82P3R43Z openfda.unii unii DQV54Y5H3U openfda.unii unii K73E24S6X9 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 or worsen. If pregnant or breastfeeding, 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.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.