Home FDA labels 2e0067b6-5a38-4cbe-845f-c02c9b8f485b BHI Arthritis 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 BHI Arthritis
Generic name ARNICA MONTANA ROOT, BERBERIS VULGARIS ROOT BARK, BRYONIA ALBA WHOLE, CAUSTICUM, CITRULLUS COLOCYNTHIS FRUIT PULP, SOLANUM DULCAMARA TOP, FERROSOFERRIC PHOSPHATE, LEDUM PALUSTRE TWIG, LYCOPODIUM CLAVATUM SPORE, RANUNCULUS BULBOSUS, RHODODENDRON AUREUM LEAF, TOXICODENDRON PUBESCENS LEAF , AND SULFUR
Manufacturer MediNatura Inc
Product type HUMAN OTC DRUG
SPL set ID d58c4651-2871-4beb-b1f5-e01a793cbc44
SPL ID 2e0067b6-5a38-4cbe-845f-c02c9b8f485b
Version 6
Effective date 2024-12-17
Source export date 2026-10-12
Source partition 12
Source file https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:56:26 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 · 23 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name BHI Arthritis openfda.brand_name generic name ARNICA MONTANA ROOT, BERBERIS VULGARIS ROOT BARK, BRYONIA ALBA WHOLE, CAUSTICUM, CITRULLUS COLOCYNTHIS FRUIT PULP, SOLANUM DULCAMARA TOP, FERROSOFERRIC PHOSPHATE, LEDUM PALUSTRE TWIG, LYCOPODIUM CLAVATUM SPORE, RANUNCULUS BULBOSUS, RHODODENDRON AUREUM LEAF, TOXICODENDRON PUBESCENS LEAF , AND SULFUR openfda.generic_name manufacturer name MediNatura Inc openfda.manufacturer_name ndc package 62795-1010-3 openfda.package_ndc ndc package 62795-1010-2 openfda.package_ndc ndc product 62795-1010 openfda.product_ndc ndc11 package 62795101003 derived:openfda.package_ndc ndc11 package 62795101002 derived:openfda.package_ndc spl id 2e0067b6-5a38-4cbe-845f-c02c9b8f485b id spl set id d58c4651-2871-4beb-b1f5-e01a793cbc44 set_id unii 877L01IZ0P openfda.unii unii DD5FO1WKFU openfda.unii unii KPS1B1162N openfda.unii unii 1TH8Q20J0U openfda.unii unii 91GQH8I5F7 openfda.unii unii 6IO182RP7A openfda.unii unii IV92NQJ73U openfda.unii unii AEQ8NXJ0MB openfda.unii unii 70FD1KFU70 openfda.unii unii 56K0VVT47P openfda.unii unii C88X29Y479 openfda.unii unii 23H32AOH17 openfda.unii unii MUE8Y11327 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 breast-feeding, ask a health professional before use. Keep out of reach of children. If symptoms persist or worsen, a health professional should be consulted. Do not use if known sensitivity to Arthritis or any of its ingredients exists.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.