Home FDA labels 0e77340b-340c-fe13-e063-6294a90a0301 N03 EXCHEM 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 N03 EXCHEM
Generic name ALLIUM SATIVUM, ARSENICUM ALBUM, BENZOICUM ACIDUM, BERBERIS VULGARIS, BETULA VERRUCOSA, CALCAREA CARBONICA, CARBOLICUM ACIDUM, CHELIDONIUM MAJUS, CHLORINUM, CITRICUM ACIDUM, HISTAMINUM, ICHTHYOLUM, JUNIPERUS COMMUNIS, LYCOPODIUM CLAVATUM, MERCURIUS SOLUBILIS, NATRUM BICARBONICUM, SODIUM HYPOCHLORITE, SOLIDAGO VIRGAUREA, SULPHUR
Manufacturer Apex Energetics Inc.
Product type HUMAN OTC DRUG
SPL set ID ba73a050-9a5d-1549-e053-2a95a90a62aa
SPL ID 0e77340b-340c-fe13-e063-6294a90a0301
Version 2
Effective date 2024-01-08
Source export date 2026-09-28
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/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:55:52 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 · 27 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name N03 EXCHEM openfda.brand_name generic name ALLIUM SATIVUM, ARSENICUM ALBUM, BENZOICUM ACIDUM, BERBERIS VULGARIS, BETULA VERRUCOSA, CALCAREA CARBONICA, CARBOLICUM ACIDUM, CHELIDONIUM MAJUS, CHLORINUM, CITRICUM ACIDUM, HISTAMINUM, ICHTHYOLUM, JUNIPERUS COMMUNIS, LYCOPODIUM CLAVATUM, MERCURIUS SOLUBILIS, NATRUM BICARBONICUM, SODIUM HYPOCHLORITE, SOLIDAGO VIRGAUREA, SULPHUR openfda.generic_name manufacturer name Apex Energetics Inc. openfda.manufacturer_name ndc package 63479-1403-1 openfda.package_ndc ndc product 63479-1403 openfda.product_ndc ndc11 package 63479140301 derived:openfda.package_ndc spl id 0e77340b-340c-fe13-e063-6294a90a0301 id spl set id ba73a050-9a5d-1549-e053-2a95a90a62aa set_id unii V1V998DC17 openfda.unii unii 7E889U5RNN openfda.unii unii 3POA0Q644U openfda.unii unii 324Y4038G2 openfda.unii unii 4R7X1O2820 openfda.unii unii NQ14646378 openfda.unii unii 8SKN0B0MIM openfda.unii unii 1TH8Q20J0U openfda.unii unii DY38VHM5OD openfda.unii unii 5HW39H9KDH openfda.unii unii 339NCG44TV openfda.unii unii 2E32821G6I openfda.unii unii S7V92P67HO openfda.unii unii HBU87MH6OY openfda.unii unii 70FD1KFU70 openfda.unii unii XF417D3PSL openfda.unii unii 8MDF5V39QO openfda.unii unii 5405K23S50 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: 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 headache, fatigue, swollen tonsils, nausea, dizziness, itching, coughing, burning pains, 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.