Home FDA labels 2c53f257-54a1-4a2b-aac3-6eaffea91603 Artalgia 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 Artalgia
Generic name CARDUUS MARIANUS, ARNICA MONTANA, AGARICUS MUSCARIUS, BARYTA CARBONICA, BELLIS PERENNIS, GLONOINUM, HAMAMELIS VIRGINIANA, MERCURIUS SOLUBILIS, PLUMBUM METALLICUM, SECALE CORNUTUM, VANADIUM METALLICUM, CARBO VEGETABILIS, HYPERICUM PERFORATUM, PHOSPHORUS PULSATILLA (PRATENSIS), RHUS TOX
Manufacturer Todd Horton DPM
Product type HUMAN OTC DRUG
SPL set ID 9404b908-5b1c-44b0-a9ff-35f3768b8ed7
SPL ID 2c53f257-54a1-4a2b-aac3-6eaffea91603
Version 1
Effective date 2020-07-15
Source export date 2026-10-12
Source partition 4
Source file https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 01:39:26 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 · 24 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Artalgia openfda.brand_name generic name CARDUUS MARIANUS, ARNICA MONTANA, AGARICUS MUSCARIUS, BARYTA CARBONICA, BELLIS PERENNIS, GLONOINUM, HAMAMELIS VIRGINIANA, MERCURIUS SOLUBILIS, PLUMBUM METALLICUM, SECALE CORNUTUM, VANADIUM METALLICUM, CARBO VEGETABILIS, HYPERICUM PERFORATUM, PHOSPHORUS PULSATILLA (PRATENSIS), RHUS TOX openfda.generic_name manufacturer name Todd Horton DPM openfda.manufacturer_name ndc package 45341-0002-1 openfda.package_ndc ndc product 45341-0002 openfda.product_ndc ndc11 package 45341000201 derived:openfda.package_ndc spl id 2c53f257-54a1-4a2b-aac3-6eaffea91603 id spl set id 9404b908-5b1c-44b0-a9ff-35f3768b8ed7 set_id unii 2P3VWU3H10 openfda.unii unii 27YLU75U4W openfda.unii unii XK4IUX8MNB openfda.unii unii 324Y4038G2 openfda.unii unii O80TY208ZW openfda.unii unii 2HU33I03UY openfda.unii unii 6P669D8HQ8 openfda.unii unii DIF093I037 openfda.unii unii U946SH95EE openfda.unii unii 6IO182RP7A openfda.unii unii 8E272251DI openfda.unii unii 2P299V784P openfda.unii unii 00J9J9XKDE openfda.unii unii G59M7S0WS3 openfda.unii unii 01G9XEA93N openfda.unii unii T7S323PKJS 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: Keep out of reach of children. In case of overdose, contact physician or Poison Control Center right away. If pregnant or breast-feeding, seek advice of a health professional before use. Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.