Home FDA labels 0e77063c-fc41-cee6-e063-6394a90a0d54 N01 PROTOMER 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 N01 PROTOMER
Generic name ADRENALINUM, ARGENTUM NITRICUM, ARNICA MONTANA, AURUM METALLICUM, AVENA SATIVA, BERBERIS VULGARIS, CHELIDONIUM MAJUS, CHININUM ARSENICOSUM, HEPAR SULPHURIS CALCAREUM, HYPERICUM PERFORATUM, NATRUM FLUORATUM, NICCOLUM METALLICUM, PASSIFLORA INCARNATA, SARSAPARILLA, SILICEA, SOLIDAGO VIRGAUREA, THUJA OCCIDENTALIS, ZINCUM VALERIANICUM
Manufacturer Apex Energetics Inc.
Product type HUMAN OTC DRUG
SPL set ID bfc8e049-2f62-31c4-e053-2a95a90a6e16
SPL ID 0e77063c-fc41-cee6-e063-6394a90a0d54
Version 2
Effective date 2024-01-08
Source export date 2026-10-12
Source partition 8
Source file https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:14:43 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 · 26 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name N01 PROTOMER openfda.brand_name generic name ADRENALINUM, ARGENTUM NITRICUM, ARNICA MONTANA, AURUM METALLICUM, AVENA SATIVA, BERBERIS VULGARIS, CHELIDONIUM MAJUS, CHININUM ARSENICOSUM, HEPAR SULPHURIS CALCAREUM, HYPERICUM PERFORATUM, NATRUM FLUORATUM, NICCOLUM METALLICUM, PASSIFLORA INCARNATA, SARSAPARILLA, SILICEA, SOLIDAGO VIRGAUREA, THUJA OCCIDENTALIS, ZINCUM VALERIANICUM openfda.generic_name manufacturer name Apex Energetics Inc. openfda.manufacturer_name ndc package 63479-1401-1 openfda.package_ndc ndc product 63479-1401 openfda.product_ndc ndc11 package 63479140101 derived:openfda.package_ndc spl id 0e77063c-fc41-cee6-e063-6394a90a0d54 id spl set id bfc8e049-2f62-31c4-e053-2a95a90a6e16 set_id unii MN0RX54EQA openfda.unii unii XK4IUX8MNB openfda.unii unii 7E889U5RNN openfda.unii unii O80TY208ZW openfda.unii unii 2H1576D5WG openfda.unii unii 8ZYQ1474W7 openfda.unii unii 1TH8Q20J0U openfda.unii unii 1NT28V9397 openfda.unii unii ETJ7Z6XBU4 openfda.unii unii 95IT3W8JZE openfda.unii unii 79Y1949PYO openfda.unii unii YKH834O4BH openfda.unii unii 42QO5P0NLM openfda.unii unii 7OV03QG267 openfda.unii unii MA9CQJ3F7F openfda.unii unii CLF5YFS11O openfda.unii unii 5405K23S50 openfda.unii unii 1MBW07J51Q 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 irritability, headache, sadness, recurrent nausea, vomiting, fear, 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.