Home FDA labels 0e765edc-2648-533a-e063-6394a90a7c53 B14 BRONCHOTOX 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 B14 BRONCHOTOX
Generic name BELLADONNA, BLATTA ORIENTALIS, COCCUS CACTI, CORALLIUM RUBRUM, CUPRUM METALLICUM, DROSERA ROTUNDIFOLIA, ECHINACEA ANGUSTIFOLIA, HEDERA HELIX, HYDRASTIS CANADENSIS, IPECACUANHA, KALI NITRICUM, LAC VACCINUM, LOBELIA INFLATA, PASSIFLORA INCARNATA, PERTUSSINUM, SAMBUCUS NIGRA, THYMUS SERPYLLUM, VALERIANA OFFICINALIS
Manufacturer Apex Energetics Inc.
Product type HUMAN OTC DRUG
SPL set ID beeaca49-a683-7e57-e053-2995a90ac04f
SPL ID 0e765edc-2648-533a-e063-6394a90a7c53
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 05:15:23 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 B14 BRONCHOTOX openfda.brand_name generic name BELLADONNA, BLATTA ORIENTALIS, COCCUS CACTI, CORALLIUM RUBRUM, CUPRUM METALLICUM, DROSERA ROTUNDIFOLIA, ECHINACEA ANGUSTIFOLIA, HEDERA HELIX, HYDRASTIS CANADENSIS, IPECACUANHA, KALI NITRICUM, LAC VACCINUM, LOBELIA INFLATA, PASSIFLORA INCARNATA, PERTUSSINUM, SAMBUCUS NIGRA, THYMUS SERPYLLUM, VALERIANA OFFICINALIS openfda.generic_name manufacturer name Apex Energetics Inc. openfda.manufacturer_name ndc package 63479-0214-1 openfda.package_ndc ndc product 63479-0214 openfda.product_ndc ndc11 package 63479021401 derived:openfda.package_ndc spl id 0e765edc-2648-533a-e063-6394a90a7c53 id spl set id beeaca49-a683-7e57-e053-2995a90ac04f set_id unii 86H4S6K51N openfda.unii unii 917J3173FT openfda.unii unii 9PP1T3TC5U openfda.unii unii 789U1901C5 openfda.unii unii 2CA71K0DLE openfda.unii unii QR44N9XPJQ openfda.unii unii LZB7TFX1LT openfda.unii unii U364V64HUN openfda.unii unii 3D10KUA6BM openfda.unii unii VB06AV5US8 openfda.unii unii ZW3Z11D0JV openfda.unii unii WQZ3G9PF0H openfda.unii unii 62I3C8233L openfda.unii unii JWF5YAW3QW openfda.unii unii RU45X2JN0Z openfda.unii unii CT03BSA18U openfda.unii unii CLF5YFS11O openfda.unii unii 535787266D 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 coughing, wheezing, congestion, 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.