Home FDA labels 47c64e74-ff74-46dc-a2c7-9574586ed7cb JOINTOX BB 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 JOINTOX BB
Generic name BAPTISIA TINCTORIA, ECHINACEA (ANGUSTIFOLIA), HYDRASTIS CANADENSIS, BORRELIA BURGDORFERI NOSODE, BABESIA MICROTI, EHRLICHIA NOSODE (CANINE), MENINGOCOCCUS NOSODE, HEPATITIS B NOSODE, ARSENICUM ALBUM, BRYONIA (ALBA), CHELIDONIUM MAJUS, COLCHICUM AUTUMNALE, KALMIA LATIFOLIA, LEDUM PALUSTRE, LYCOPODIUM CLAVATUM, PHOSPHORUS, RHUS TOX
Manufacturer Energique, Inc.
Product type HUMAN OTC DRUG
SPL set ID c20ef937-057f-4577-b2b7-71a82ed381bf
SPL ID 47c64e74-ff74-46dc-a2c7-9574586ed7cb
Version 3
Effective date 2023-08-15
Source export date 2026-10-12
Source partition 3
Source file https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 01:32:30 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 · 25 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name JOINTOX BB openfda.brand_name generic name BAPTISIA TINCTORIA, ECHINACEA (ANGUSTIFOLIA), HYDRASTIS CANADENSIS, BORRELIA BURGDORFERI NOSODE, BABESIA MICROTI, EHRLICHIA NOSODE (CANINE), MENINGOCOCCUS NOSODE, HEPATITIS B NOSODE, ARSENICUM ALBUM, BRYONIA (ALBA), CHELIDONIUM MAJUS, COLCHICUM AUTUMNALE, KALMIA LATIFOLIA, LEDUM PALUSTRE, LYCOPODIUM CLAVATUM, PHOSPHORUS, RHUS TOX openfda.generic_name manufacturer name Energique, Inc. openfda.manufacturer_name ndc package 44911-0588-1 openfda.package_ndc ndc product 44911-0588 openfda.product_ndc ndc11 package 44911058801 derived:openfda.package_ndc spl id 47c64e74-ff74-46dc-a2c7-9574586ed7cb id spl set id c20ef937-057f-4577-b2b7-71a82ed381bf set_id unii 27YLU75U4W openfda.unii unii 877L01IZ0P openfda.unii unii 7E889U5RNN openfda.unii unii 993QHL78E6 openfda.unii unii 79N6542N18 openfda.unii unii 6IO182RP7A openfda.unii unii S7V92P67HO openfda.unii unii VB06AV5US8 openfda.unii unii 1948X6KEG3 openfda.unii unii 77H9EM77P7 openfda.unii unii ZW3Z11D0JV openfda.unii unii T7J046YI2B openfda.unii unii 5EF0HWI5WU openfda.unii unii 970Y8T1JZY openfda.unii unii C88X29Y479 openfda.unii unii 0J8NV9V5Q8 openfda.unii unii V3TP2MD7F3 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. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.