Home FDA labels 58c9fce8-56a5-4d51-e063-6294a90a7f46 Thyropath 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 Thyropath
Generic name AVENA SATIVA, BORAGO OFFICINALIS, CALCAREA CARBONICA, CHELIDONIUM MAJUS, FERRUM IODATUM, FUCUS VESICULOSUS, GLANDULA SUPRARENALIS SUIS, HEPAR SUIS, IODIUM, KALI IODATUM, PHOSPHORICUM ACIDUM, PITUITARUM POSTERIUM (BOVINE), PYRIDOXINUM HYDROCHLORICUM, THYROIDINUM (BOVINE), ZINCUM METALLICUM
Manufacturer Energetix Corporation
Product type HUMAN OTC DRUG
SPL set ID f8ec1c51-520c-4bbe-8701-e875ea88a628
SPL ID 58c9fce8-56a5-4d51-e063-6294a90a7f46
Version 12
Effective date 2026-08-11
Source export date 2026-09-28
Source partition 7
Source file https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:48:19 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 Thyropath openfda.brand_name generic name AVENA SATIVA, BORAGO OFFICINALIS, CALCAREA CARBONICA, CHELIDONIUM MAJUS, FERRUM IODATUM, FUCUS VESICULOSUS, GLANDULA SUPRARENALIS SUIS, HEPAR SUIS, IODIUM, KALI IODATUM, PHOSPHORICUM ACIDUM, PITUITARUM POSTERIUM (BOVINE), PYRIDOXINUM HYDROCHLORICUM, THYROIDINUM (BOVINE), ZINCUM METALLICUM openfda.generic_name manufacturer name Energetix Corporation openfda.manufacturer_name ndc package 64578-0133-1 openfda.package_ndc ndc product 64578-0133 openfda.product_ndc ndc11 package 64578013301 derived:openfda.package_ndc spl id 58c9fce8-56a5-4d51-e063-6294a90a7f46 id spl set id f8ec1c51-520c-4bbe-8701-e875ea88a628 set_id unii 7E889U5RNN openfda.unii unii 7JM57I419K openfda.unii unii PB618V0K2W openfda.unii unii 9679TC07X4 openfda.unii unii MN18OTN73W openfda.unii unii 2E32821G6I openfda.unii unii 535G2ABX9M openfda.unii unii 398IYQ16YV openfda.unii unii 1C4QK22F9J openfda.unii unii MA9CQJ3F7F openfda.unii unii E4GA8884NN openfda.unii unii 68Y4CF58BV openfda.unii unii J41CSQ7QDS openfda.unii unii 6EC706HI7F openfda.unii unii F5452U54PN 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 In case of overdose, get medical help or contact a Poison Control Center right away. If pregnant or breast-feeding , ask a healthcare professional before use. Keep out of reach of children.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.