Bone Support HP

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: Bone Support HP
Generic name: 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
Manufacturer: Energique, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: da6937b9-da23-4e78-96af-2ca40f973a02
SPL ID: 14603ca2-3c57-43a1-8466-2be35f90a3cd
Version: 3
Effective date: 2024-09-30
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:18:14

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 · 21 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Bone Support HP	openfda.brand_name
generic name		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	openfda.generic_name
manufacturer name		Energique, Inc.	openfda.manufacturer_name
ndc	package	44911-0663-1	openfda.package_ndc
ndc	product	44911-0663	openfda.product_ndc
ndc11	package	44911066301	derived:openfda.package_ndc
spl id		14603ca2-3c57-43a1-8466-2be35f90a3cd	id
spl set id		da6937b9-da23-4e78-96af-2ca40f973a02	set_id
unii		O3B55K4YKI	openfda.unii
unii		91D9GV0Z28	openfda.unii
unii		N94C2U587S	openfda.unii
unii		HF539G9L3Q	openfda.unii
unii		ETJ7Z6XBU4	openfda.unii
unii		RGL5YE86CZ	openfda.unii
unii		M9VVZ08EKQ	openfda.unii
unii		2E32821G6I	openfda.unii
unii		6IO182RP7A	openfda.unii
unii		C21158IIRK	openfda.unii
unii		E4GA8884NN	openfda.unii
unii		1W0775VX6E	openfda.unii
unii		41YPU4MMCA	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: 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.

Reported adverse events (FAERS/openFDA)#

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