Home FDA labels 7877d648-d76c-48d5-9333-c77697ab21c6 Jointforce R 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 Jointforce R
Generic name CHONDRUS CRISPUS, CIMICIFUGA RACEMOSA, SPIRAEA ULMARIA, TRIFOLIUM PRATENSE, URTICA URENS, XANTHOXYLUM FRAXINEUM, SYMPHYTUM OFFICINALE, COLCHICUM AUTUMNALE, FERRUM PHOSPHORICUM, FORMICA RUFA, LITHIUM CARBONICUM, NATRUM SULPHURICUM, RHODODENDRON CHRYSANTHEMUM, RHUS TOX
Manufacturer BioActive Nutritional, Inc.
Product type HUMAN OTC DRUG
SPL set ID 26a45f44-4c9e-420d-aa76-9d3a67326d12
SPL ID 7877d648-d76c-48d5-9333-c77697ab21c6
Version 3
Effective date 2026-03-05
Source export date 2026-10-12
Source partition 6
Source file https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 01:47:11 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 · 22 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Jointforce R openfda.brand_name generic name CHONDRUS CRISPUS, CIMICIFUGA RACEMOSA, SPIRAEA ULMARIA, TRIFOLIUM PRATENSE, URTICA URENS, XANTHOXYLUM FRAXINEUM, SYMPHYTUM OFFICINALE, COLCHICUM AUTUMNALE, FERRUM PHOSPHORICUM, FORMICA RUFA, LITHIUM CARBONICUM, NATRUM SULPHURICUM, RHODODENDRON CHRYSANTHEMUM, RHUS TOX openfda.generic_name manufacturer name BioActive Nutritional, Inc. openfda.manufacturer_name ndc package 43857-0602-1 openfda.package_ndc ndc product 43857-0602 openfda.product_ndc ndc11 package 43857060201 derived:openfda.package_ndc spl id 7877d648-d76c-48d5-9333-c77697ab21c6 id spl set id 26a45f44-4c9e-420d-aa76-9d3a67326d12 set_id unii 997724QNDS openfda.unii unii A4KL1HMZ7T openfda.unii unii 993QHL78E6 openfda.unii unii 0YPR65R21J openfda.unii unii OQS23HUA1X openfda.unii unii M9VVZ08EKQ openfda.unii unii IHN2NQ5OF9 openfda.unii unii 55H0W83JO5 openfda.unii unii 91GQH8I5F7 openfda.unii unii 6IO182RP7A openfda.unii unii IV92NQJ73U openfda.unii unii 4JS0838828 openfda.unii unii 2BMD2GNA4V openfda.unii unii K73E24S6X9 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 care 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.