Home FDA labels 0e773c6a-016f-fae5-e063-6294a90af595 M12 BRAIN 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 M12 BRAIN
Generic name ARGENTUM METALLICUM, ARTEMISIA VULGARIS, CICUTA VIROSA, COBALTUM METALLICUM, COCCULUS INDICUS, CONIUM MACULATUM, GINKGO BILOBA, KALI BROMATUM, LATHYRUS SATIVUS, MERCURIUS SOLUBILIS, NUX VOMICA, PLUMBUM METALLICUM, SALIX ALBA, SCOPOLAMINUM HYDROBROMIDUM, SEQUOIADENDRON GIGANTEUM, SUS SCROFA CEREBRUM
Manufacturer Apex Energetics Inc
Product type HUMAN OTC DRUG
SPL set ID ba72bba7-177e-4f83-e053-2995a90a86ec
SPL ID 0e773c6a-016f-fae5-e063-6294a90af595
Version 2
Effective date 2024-01-08
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 05:15:19 Harmonized routes table Harmonized routes SUBLINGUAL
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 · 24 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name M12 BRAIN openfda.brand_name generic name ARGENTUM METALLICUM, ARTEMISIA VULGARIS, CICUTA VIROSA, COBALTUM METALLICUM, COCCULUS INDICUS, CONIUM MACULATUM, GINKGO BILOBA, KALI BROMATUM, LATHYRUS SATIVUS, MERCURIUS SOLUBILIS, NUX VOMICA, PLUMBUM METALLICUM, SALIX ALBA, SCOPOLAMINUM HYDROBROMIDUM, SEQUOIADENDRON GIGANTEUM, SUS SCROFA CEREBRUM openfda.generic_name manufacturer name Apex Energetics Inc openfda.manufacturer_name ndc package 63479-1312-1 openfda.package_ndc ndc product 63479-1312 openfda.product_ndc ndc11 package 63479131201 derived:openfda.package_ndc spl id 0e773c6a-016f-fae5-e063-6294a90af595 id spl set id ba72bba7-177e-4f83-e053-2995a90a86ec set_id unii 4GB5DQR532 openfda.unii unii 3M4G523W1G openfda.unii unii 269XH13919 openfda.unii unii OSD78555ZM openfda.unii unii 324Y4038G2 openfda.unii unii Q28R5GF371 openfda.unii unii 451IFR0GXB openfda.unii unii 3G0H8C9362 openfda.unii unii 2P299V784P openfda.unii unii 8VP54WOT4I openfda.unii unii 19FUJ2C58T openfda.unii unii 810258W28U openfda.unii unii 205MXS71H7 openfda.unii unii 6CO90XQD9O openfda.unii unii YEA9P21S8N openfda.unii unii 32MP823R8S 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: If pregnant or breastfeeding , ask a health professional before use. Do not use if clear seal over the cap is broken or missing. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Stop use and ask a doctor if brain fog, forgetfulness, headache, dizziness, irritability, feeling low-spirited, or other symptoms do not improve within 7 days or are accompanied by fever.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.