64578-0146 NDC - CIRCULOPATH (ADENOSINUM CYCLOPHOSPHORICUM, ARNICA MONTANA, AURUM MURIATICUM, BARYTA MURIATICA, BORAGO OFFICINALIS, CHOLESTERINUM, CITRUS LIMONUM, HYPOTHALAMUS (BOVINE), KALI IODATUM, LAUROCERASUS, MAGNESIA MURIATICA, NADIDUM, PHASEOLUS, PHOSPHORUS, THYROIDINUM (BOVINE))

Drug Information

  • Product NDC: 64578-0146
  • Proprietary Name: Circulopath
  • Non Proprietary Name: Adenosinum cyclophosphoricum, Arnica montana, Aurum muriaticum, Baryta muriatica, Borago officinalis, Cholesterinum, Citrus limonum, Hypothalamus (Bovine), Kali iodatum, Laurocerasus, Magnesia muriatica, Nadidum, Phaseolus, Phosphorus, Thyroidinum (Bovine)
  • Active Ingredient(s): 10 [hp_X]/59.1mL ADENOSINE CYCLIC PHOSPHATE; 30 [hp_X]/59.1mL ARNICA MONTANA; 12 [hp_X]/59.1mL BARIUM CHLORIDE DIHYDRATE; 6 [hp_X]/59.1mL BORAGE; 12 [hp_X]/59.1mL BOS TAURUS HYPOTHALAMUS; 12 [hp_X]/59.1mL CHOLESTEROL; 10 [hp_X]/59.1mL COENZYME A; 12 [hp_X]/59.1mL CONIUM MACULATUM FLOWERING TOP; 6 [hp_X]/59.1mL DIGITALIS; 4 [hp_X]/59.1mL GINKGO; 12 [hp_X]/59.1mL GOLD TRICHLORIDE; 5 [hp_X]/59.1mL KIDNEY BEAN; 4 [hp_X]/59.1mL LEMON JUICE; 8 [hp_X]/59.1mL MAGNESIUM CHLORIDE; 9 [hp_X]/59.1mL NADIDE; 30 [hp_X]/59.1mL PHOSPHORUS; 12 [hp_X]/59.1mL POTASSIUM IODIDE; 10 [hp_X]/59.1mL PRUNUS LAUROCERASUS LEAF; 12 [hp_X]/59.1mL THYROID, BOVINE
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Calculi Dissolution Agent [EPC]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Increased Histamine Release [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]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Plant Proteins [CS]; Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]; Vegetable Proteins [CS]

Labeler Information

Field Name Field Value
Labeler Name: Energetix Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:6/20/2016

Package Information

No. Package Code Package Description Billing Unit
164578-0146-159.1 mL in 1 BOTTLE, DROPPER (64578-0146-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC64578-0146The 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 NAMECirculopathThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAdenosinum cyclophosphoricum, Arnica montana, Aurum muriaticum, Baryta muriatica, Borago officinalis, Cholesterinum, Citrus limonum, Hypothalamus (Bovine), Kali iodatum, Laurocerasus, Magnesia muriatica, Nadidum, Phaseolus, Phosphorus, Thyroidinum (Bovine)The 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 DATE6/20/2016This 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 NAMEEnergetix CorporationName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEADENOSINE CYCLIC PHOSPHATE; ARNICA MONTANA; BARIUM CHLORIDE DIHYDRATE; BORAGE; BOS TAURUS HYPOTHALAMUS; CHOLESTEROL; COENZYME A; CONIUM MACULATUM FLOWERING TOP; DIGITALIS; GINKGO; GOLD TRICHLORIDE; KIDNEY BEAN; LEMON JUICE; MAGNESIUM CHLORIDE; NADIDE; PHOSPHORUS; POTASSIUM IODIDE; PRUNUS LAUROCERASUS LEAF; THYROID, BOVINEAn 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 STRENGTH10; 30; 12; 6; 12; 12; 10; 12; 6; 4; 12; 5; 4; 8; 9; 30; 12; 10; 12 
ACTIVE INGRED UNIT[hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL 
PHARM CLASSESAllergens [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [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], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE], Vegetable Proteins [CS] 

Download Record

Download this NDC record record in Text format: Export

Download this NDC record record in Excel (CSV) format: Export

Download this NDC record record in XML format: Export

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

Previous Code
Next Code