Spinapar

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2024-10-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:28:40

Label at a glance#

ProductSpinapar
Active ingredientHORSE CHESTNUT, HARPAGOPHYTUM PROCUMBENS ROOT, PHYTOLACCA AMERICANA ROOT, RUTA GRAVEOLENS FLOWERING TOP, SUS SCROFA CARTILAGE, SUS SCROFA INTERVERTEBRAL DISC, AMANITA MUSCARIA FRUITING BODY, SILVER, ARNICA MONTANA WHOLE, BAMBUSA BAMBOS LEAF, BAMBUSA BAMBOS SAP, BELLIS PERENNIS WHOLE, BRYONIA ALBA ROOT, CALCIUM FLUORIDE, HYPERICUM PERFORATUM WHOLE, TOXICODENDRON PUBESCENS LEAF, SULFUR, TELLURIUM
Label structure9 sections

Dosage and administration

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

(in each drop): 5.88% of Aesculus Hippocastanum 4X, Agaricus Muscarius 12X, Argentum Metallicum 12X, Arnica Montana 12X, Bambusa Arundinacea 12X, Bellis Perennis 12X, Bryonia (Alba) 12X, Calcarea Fluorica 12X, Cartilago Suis 6X, Discus Intervertebralis Suis 6X, Harpagophytum 4X, Hypericum Perforatum 12X, Phytolacca Decandra 4X, Rhus Tox 12X, Ruta Graveolens 4X, Sulphur 12X, Tellurium Metallicum 12X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve minor back pain, stiffness, numbness or tingling.**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

WARNINGS:

WARNINGS SECTION

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.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

INDICATIONS:

INDICATIONS & USAGE SECTION

May temporarily relieve minor back pain, stiffness, numbness or tingling.**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized water, 20% Ethanol.

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. by Energique, Inc.

201 Apple Blvd.

Woodbine, IA 51579 800-869-8078

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ENERGIQUE

SINCE 1987

HOMEOPATHIC REMEDY

SPINAPAR

1 fl. oz. (30 ml)

SpinaparSpinapar

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0659-12024-10-30C16284748780-11030e365-3566-111a-e063-dadaa90a10e2DRUG FACTS:
44911-0659-12024-01-30C16284748780-11030e365-3566-111a-e063-dadaa90a10e2DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0659-1Spinapar30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0659SPINAPAR (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) LIQUID [ENERGIQUE, INC.]2Current NDC, Legacy NDC, 1 package rows20241101_e3e1da2e-965b-4be7-a43d-a6cef4692248.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-065944911-0659-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SpinaparAESCULUS 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 METALLICUMEnergique, Inc.e3e1da2e-965b-4be7-a43d-a6cef46922482024-10-30WarningsExact identifier
ndc (package): 44911-0659-1
ndc (product): 44911-0659
ndc11 (package): 44911065901
spl id: fefaacf7-d239-4245-916e-49d748c75ea5
spl set id: e3e1da2e-965b-4be7-a43d-a6cef4692248

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.