Home FDA labels fefaacf7-d239-4245-916e-49d748c75ea5 Spinapar 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 Spinapar
Generic name AESCULUS HIPPOCASTANUM, HARPAGOPHYTUM, PHYTOLACCA DECANDRA, RUTA GRAVEOLENS, CARTILAGO SUIS, DISCUS INTERVERTEBRALIS SUIS, AGARICUS MUSCARIUS, ARGENTUM METALLICUM, ARNICA MONTANA, BAMBUSA ARUNDINACEA, BELLIS PERENNIS, BRYONIA (ALBA), CALCAREA FLUORICA, HYPERICUM PERFORATUM, RHUS TOX, SULPHUR, TELLURIUM METALLICUM
Manufacturer Energique, Inc.
Product type HUMAN OTC DRUG
SPL set ID e3e1da2e-965b-4be7-a43d-a6cef4692248
SPL ID fefaacf7-d239-4245-916e-49d748c75ea5
Version 2
Effective date 2024-10-30
Source export date 2026-09-28
Source partition 7
Source file https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:48:03 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 · 26 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Spinapar openfda.brand_name generic name AESCULUS HIPPOCASTANUM, HARPAGOPHYTUM, PHYTOLACCA DECANDRA, RUTA GRAVEOLENS, CARTILAGO SUIS, DISCUS INTERVERTEBRALIS SUIS, AGARICUS MUSCARIUS, ARGENTUM METALLICUM, ARNICA MONTANA, BAMBUSA ARUNDINACEA, BELLIS PERENNIS, BRYONIA (ALBA), CALCAREA FLUORICA, HYPERICUM PERFORATUM, RHUS TOX, SULPHUR, TELLURIUM METALLICUM openfda.generic_name manufacturer name Energique, Inc. openfda.manufacturer_name ndc package 44911-0659-1 openfda.package_ndc ndc product 44911-0659 openfda.product_ndc ndc11 package 44911065901 derived:openfda.package_ndc spl id fefaacf7-d239-4245-916e-49d748c75ea5 id spl set id e3e1da2e-965b-4be7-a43d-a6cef4692248 set_id unii 3M4G523W1G openfda.unii unii OJ17O2WTSM openfda.unii unii 11E6VI8VEG openfda.unii unii XK4IUX8MNB openfda.unii unii O3B55K4YKI openfda.unii unii O80TY208ZW openfda.unii unii 2HU33I03UY openfda.unii unii 3C18L6RJAZ openfda.unii unii DIF093I037 openfda.unii unii N94C2U587S openfda.unii unii 1OYM338E89 openfda.unii unii 6IO182RP7A openfda.unii unii 73ECW5WG2F openfda.unii unii DPQ0BJD6MR openfda.unii unii T7J046YI2B openfda.unii unii 70FD1KFU70 openfda.unii unii HW86D1FGSS openfda.unii unii NQA0O090ZJ 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. 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.