Bone Support

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2024-09-30
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:28:08

Label at a glance#

ProductBone Support HP
Active ingredientOYSTER SHELL CALCIUM CARBONATE, CRUDE, CALCIUM FLUORIDE, TRIBASIC CALCIUM PHOSPHATE, EUPATORIUM PERFOLIATUM FLOWERING TOP, HEKLA LAVA, HYDROFLUORIC ACID, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, PHOSPHORIC ACID, TOXICODENDRON PUBESCENS LEAF, RUTA GRAVEOLENS FLOWERING TOP, SILICON DIOXIDE, STRONTIUM CARBONATE, COMFREY ROOT
Label structure9 sections

Indications and uses

May temporarily relieve discomfort due to bone trauma and backache.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Dosage and administration

• Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a 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): Calcarea Carbonica 30X 7.69%, Calcarea Fluorica 30X 7.69%, Calcarea Phosphorica 30X 7.69%, Eupatorium Perfoliatum 30X 7.69%, Hekla Lava 30X 7.69%, Hydrofluoricum Acidum 30X 7.69%, Magnesia Phosphorica 30X 7.69%, Phosphoricum Acidum 30X 7.69%, Rhus Tox 30X 7.69%, Ruta Graveolens 30X 7.69%, Silicea 30X 7.69%, Strontium Carbonicum 30X 7.69%, Symphytum Officinale 30X 7.69%.

PURPOSE:

OTC - PURPOSE SECTION

Calcarea Carbonica - lameness,** Calcarea Fluorica – bone spurs,** Calcarea Phosphorica – growing pains,** Eupatorium Perfoliatum – bone aches,** Hekla Lava – jaw pain,** Hydrofluoricum Acidum - swelling,** Magnesia Phosphorica – cramping pains,** Phosphoricum Acidum - fatigue,** Rhus Tox - stiffness,** Ruta Graveolens – joint pain,** Silicea - backache,** Strontium Carbonicum – ankle weakness,** Symphytum Officinale – bone injuries.**

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

USES:

INDICATIONS & USAGE SECTION

May temporarily relieve discomfort due to bone trauma and backache.**

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

WARNINGS:

WARNINGS SECTION

Stop use and ask a doctor if symptons persist for more than 7 days.

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

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. 

• Consult a physician for use in children under 12 years of age.

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

BONE SUPPORT HP

1 fl. oz. (30 ml)

BONE SUPPORT HPBONE SUPPORT HP

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6e3c022f-0786-43f1-8857-edff89d5153fProduct name120260309
95250459-30e4-45c1-b08a-993044f49109Product name220250805
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334fe8d2-68fb-4331-a576-420e302ec069Product name720240320
efd58652-cb8f-4018-91ca-4b0eb2ff729fProduct name720240226
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
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c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0663-12024-07-22C16284748780-11030e365-2988-111a-e063-dadaa90a10e2DRUG FACTS:
44911-0663-12024-01-30C16284748780-11030e365-2988-111a-e063-dadaa90a10e2DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0663-1Bone SupportHP30 mL in 1 BOTTLE, DROPPERLIQUID303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0663BONE SUPPORT HP (CALCAREA CARBONICA, CALCAREA FLUORICA, CALCAREA PHOSPHORICA, EUPATORIUM PERFOLIATUM, HEKLA LAVA, HYDROFLUORICUM ACIDUM, MAGNESIA PHOSPHORICA, PHOSPHORICUM ACIDUM, RHUS TOX, RUTA GRAVEOLENS, SILICEA, STRONTIUM CARBONICUM, SYMPHYTUM OFFICINALE) LIQUID [ENERGIQUE, INC.]3Current NDC, Legacy NDC, 1 package rows20241001_da6937b9-da23-4e78-96af-2ca40f973a02.zip

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-066344911-0663-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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
Bone Support HPCALCAREA CARBONICA, CALCAREA FLUORICA, CALCAREA PHOSPHORICA, EUPATORIUM PERFOLIATUM, HEKLA LAVA, HYDROFLUORICUM ACIDUM, MAGNESIA PHOSPHORICA, PHOSPHORICUM ACIDUM, RHUS TOX, RUTA GRAVEOLENS, SILICEA, STRONTIUM CARBONICUM, SYMPHYTUM OFFICINALEEnergique, Inc.da6937b9-da23-4e78-96af-2ca40f973a022024-09-30WarningsExact identifier
ndc (package): 44911-0663-1
ndc (product): 44911-0663
ndc11 (package): 44911066301
spl id: 14603ca2-3c57-43a1-8466-2be35f90a3cd
spl set id: da6937b9-da23-4e78-96af-2ca40f973a02

Reported adverse events (FAERS/openFDA)#

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