Muscle and Joint Pain Relief

Manufacturer
Beaumont Bio Med | King Bio Inc.
Effective date
2016-09-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:08:09

Label at a glance#

ProductMuscle and Joint Pain Relief
Active ingredientHORSE CHESTNUT, ARNICA MONTANA, BELLIS PERENNIS, BRYONIA ALBA ROOT, OYSTER SHELL CALCIUM CARBONATE, CRUDE, CALCIUM FLUORIDE, BLACK COHOSH, COBALT, PSEUDOGNAPHALIUM OBTUSIFOLIUM, HYPERICUM PERFORATUM, POTASSIUM CARBONATE, POTASSIUM PHOSPHATE, DIBASIC, COW MILK, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, OXALIC ACID DIHYDRATE, PHOSPHORUS, TOXICODENDRON PUBESCENS LEAF, RUTA GRAVEOLENS FLOWERING TOP, ZINC
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

HPUS active ingredients: Aesculus hippocastanum, Arnica montana, Bellis perennis, Bryonia, Calcarea carbonica, Calcarea fluorica, Cimicifuga racemosa, Cobaltum metallicum, Gnaphalium polycephalum, Hypericum perforatum, Kali carbonicum, Kali phosphoricum, Lac vaccinum, Magnesia phosphorica, Oxalicum acidum, Phosphorus, Rhus toxicodendron, Ruta graveolens, Zincum metallicum​​. Equal volumes of each ingredient in 10X, 30X, 100X potencies.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Alcohol @ 20% (v/v), Glycerin @ 8% (v/v), in a pure water base.

INDICATIONS & USAGE SECTION

Indications: For temporary relief of: symptoms of muscle, joint pain and discomfort.

DOSAGE & ADMINISTRATION SECTION

Directions:

  • Hold close to mouth and spray 1 dose (3 complete pump sprays) directly in mouth 4-6 times daily until symptoms improve.
  • Before initial dose, depress pump 4-5 times or until primed.
  • Consult a physician for use in children under 12 years of age.

Use according to label indications and/or standard homeopathic indications.

WARNINGS SECTION

Warnings: Stop use and ask a doctor if symptoms persist or worsen. If pregnant or breast feeding, consult a healthcare professional.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep this and all medications out of the reach of children.

OTHER SAFETY INFORMATION

Other information: Tamper resistant for your protection. Use only if safety seal is intact.

OTC - PURPOSE SECTION

For temporary relief of:

  • symptoms of muscle, joint pain and discomfort

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58066-7041-72020-01-31C16284748780-19d75b9d0-a4e9-f424-e053-dadaa90a57ceMuscle and Joint Pain Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58066-7041-7Muscle and Joint Pain Relief59.2 mL in 1 BOTTLE, SPRAYLIQUID59.21

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58066-7041MUSCLE AND JOINT PAIN RELIEF (AESCULUS HIPPOCASTANUM, ARNICA MONTANA, BELLIS PERENNIS, BRYONIA, CALCAREA CARBONICA, CALCAREA FLUORICA, CIMICIFUGA RACEMOSA, COBALTUM METALLICUM, GNAPHALIUM POLYCEPHALUM, HYPERICUM PERFORATUM, KALI CARBONICUM, KALI PHOSPHORICUM, LAC VACCINUM, MAGNESIA PHOSPHORICA, OXALICUM ACIDUM, PHOSPHORUS, RHUS TOXICODENDRON, RUTA GRAVEOLENS, ZINCUM METALLICUM) LIQUID [BEAUMONT BIO MED]1Legacy NDC, 1 package rows20160909_b7a70970-c982-4e19-84de-eb0577fed1bd.zip

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58066-704158066-7041-7

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Source Document#

Source XML · Source PDF

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
9dcc7484-600c-4d4c-b2d9-10169649782cb7a70970-c982-4e19-84de-eb0577fed1bd2016-09-09WarningsExact identifier
spl id: 9dcc7484-600c-4d4c-b2d9-10169649782c
spl set id: b7a70970-c982-4e19-84de-eb0577fed1bd

Reported adverse events (FAERS/openFDA)#

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