Home FDA labels 468d36ba-2543-ef9d-e063-6394a90a19a5 Endopath-M 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 Endopath-M
Generic name ADENOSINUM CYCLOPHOSPHORICUM, AGNUS CASTUS, ASPARAGUS OFFICINALIS, AVENA SATIVA, CADMIUM METALLICUM, DAMIANA, GLANDULA SUPRARENALIS SUIS, JUNIPERUS COMMUNIS, LYCOPODIUM CLAVATUM, ORCHITINUM (BOVINE), PETROSELINUM SATIVUM, PITUITARUM POSTERIUM (BOVINE), PULSATILLA (VULGARIS), SABAL SERRULATA, SARSAPARILLA (SMILAX REGELII)
Manufacturer Energetix Corporation
Product type HUMAN OTC DRUG
SPL set ID ece117c4-5116-458e-888a-5ff3cf0cfbfb
SPL ID 468d36ba-2543-ef9d-e063-6394a90a19a5
Version 17
Effective date 2025-12-22
Source export date 2026-09-28
Source partition 2
Source file https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:15:21 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 Endopath-M openfda.brand_name generic name ADENOSINUM CYCLOPHOSPHORICUM, AGNUS CASTUS, ASPARAGUS OFFICINALIS, AVENA SATIVA, CADMIUM METALLICUM, DAMIANA, GLANDULA SUPRARENALIS SUIS, JUNIPERUS COMMUNIS, LYCOPODIUM CLAVATUM, ORCHITINUM (BOVINE), PETROSELINUM SATIVUM, PITUITARUM POSTERIUM (BOVINE), PULSATILLA (VULGARIS), SABAL SERRULATA, SARSAPARILLA (SMILAX REGELII) openfda.generic_name manufacturer name Energetix Corporation openfda.manufacturer_name ndc package 64578-0099-1 openfda.package_ndc ndc product 64578-0099 openfda.product_ndc ndc11 package 64578009901 derived:openfda.package_ndc spl id 468d36ba-2543-ef9d-e063-6394a90a19a5 id spl set id ece117c4-5116-458e-888a-5ff3cf0cfbfb set_id unii J7WWH9M8QS openfda.unii unii 00BH33GNGH openfda.unii unii Z1EJP3037Z openfda.unii unii 2H1576D5WG openfda.unii unii L0PFEMQ1DT openfda.unii unii PR4RXL6G2H openfda.unii unii 433OSF3U8A openfda.unii unii 398IYQ16YV openfda.unii unii E0399OZS9N openfda.unii unii 1WZA4Y92EX openfda.unii unii MA9CQJ3F7F openfda.unii unii O84B5194RL openfda.unii unii RQ2CFA7WWJ openfda.unii unii I76KB35JEV openfda.unii unii C88X29Y479 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.