44911-0663 NDC - BONE SUPPORT (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)

Drug Information

  • Product NDC: 44911-0663
  • Proprietary Name: Bone Support
  • Non Proprietary 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
  • Active Ingredient(s): 30 [hp_X]/mL CALCIUM FLUORIDE; 30 [hp_X]/mL COMFREY ROOT; 30 [hp_X]/mL EUPATORIUM PERFOLIATUM FLOWERING TOP; 30 [hp_X]/mL HEKLA LAVA; 30 [hp_X]/mL HYDROFLUORIC ACID; 30 [hp_X]/mL MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; 30 [hp_X]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE; 30 [hp_X]/mL PHOSPHORIC ACID; 30 [hp_X]/mL RUTA GRAVEOLENS FLOWERING TOP; 30 [hp_X]/mL SILICON DIOXIDE; 30 [hp_X]/mL STRONTIUM CARBONATE; 30 [hp_X]/mL TOXICODENDRON PUBESCENS LEAF; 30 [hp_X]/mL TRIBASIC CALCIUM PHOSPHATE
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Blood Coagulation Factor [EPC]; Calcium [CS]; Calculi Dissolution Agent [EPC]; Cations; Divalent [CS]; Increased Coagulation Factor Activity [PE]; Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]; Magnesium Ion Exchange Activity [MoA]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Phosphate Binder [EPC]; Phosphate Chelating Activity [MoA]; Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Labeler Information

Field Name Field Value
Labeler Name: Energique, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:11/9/2022

Package Information

No. Package Code Package Description Billing Unit
144911-0663-130 mL in 1 BOTTLE, DROPPER (44911-0663-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC44911-0663The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEBone SupportThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXHPA suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
NON PROPRIETARY NAMECalcarea Carbonica, Calcarea Fluorica, Calcarea Phosphorica, Eupatorium Perfoliatum, Hekla Lava, Hydrofluoricum Acidum, Magnesia Phosphorica, Phosphoricum Acidum, Rhus Tox, Ruta Graveolens, Silicea, Strontium Carbonicum, Symphytum OfficinaleThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE11/9/2022This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMEEnergique, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMECALCIUM FLUORIDE; COMFREY ROOT; EUPATORIUM PERFOLIATUM FLOWERING TOP; HEKLA LAVA; HYDROFLUORIC ACID; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHOSPHORIC ACID; RUTA GRAVEOLENS FLOWERING TOP; SILICON DIOXIDE; STRONTIUM CARBONATE; TOXICODENDRON PUBESCENS LEAF; TRIBASIC CALCIUM PHOSPHATEAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESBlood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] 

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This page was last updated on: 12/6/2025

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