64578-0158 NDC - BACTERIA-CHORD (AZADIRACHTA, BELLADONNA, BERBER VULG, BOLDO, CANDIDA ALB, CEANOTHUS, CETRARIA, CROTALUS HOR , ECHINACEA, GLANDULA SUPRARENALIS SUIS, GLYCYRRHIZA, HAMAMELIS, HEPAR SUIS, HYDRASTIS, HYDROCOTYLE, HYPERICUM, LAPPA, LEDUM, MILLEFOLIUM, MORBILLINUM, MYRRHA, PANCREAS, PERTUSSINUM, PHOS, PLANTAGO, PYROGENIUM, SOLIDAGO, ZINGIBER)

Drug Information

  • Product NDC: 64578-0158
  • Proprietary Name: Bacteria-Chord
  • Non Proprietary Name: Azadirachta, Belladonna, Berber vulg, Boldo, Candida alb, Ceanothus, Cetraria, Crotalus hor , Echinacea, Glandula suprarenalis suis, Glycyrrhiza, Hamamelis, Hepar suis, Hydrastis, Hydrocotyle, Hypericum, Lappa, Ledum, Millefolium, Morbillinum, Myrrha, Pancreas, Pertussinum, Phos, Plantago, Pyrogenium, Solidago, Zingiber
  • Active Ingredient(s): 12 [hp_X]/59.1mL ACHILLEA MILLEFOLIUM WHOLE; 4 [hp_X]/59.1mL ARCTIUM LAPPA ROOT; 8 [hp_X]/59.1mL ATROPA BELLADONNA; 8 [hp_X]/59.1mL AZADIRACHTA INDICA BARK; 9 [hp_X]/59.1mL BERBERIS VULGARIS ROOT BARK; 30 [hp_X]/59.1mL CANDIDA ALBICANS; 4 [hp_X]/59.1mL CEANOTHUS AMERICANUS LEAF; 6 [hp_X]/59.1mL CENTELLA ASIATICA; 12 [hp_X]/59.1mL CETRARIA ISLANDICA WHOLE; 12 [hp_X]/59.1mL CROTALUS HORRIDUS HORRIDUS VENOM; 4 [hp_X]/59.1mL ECHINACEA, UNSPECIFIED; 6 [hp_X]/59.1mL GINGER; 4 [hp_X]/59.1mL GLYCYRRHIZA GLABRA; 5 [hp_X]/59.1mL GOLDENSEAL; 6 [hp_X]/59.1mL HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; 30 [hp_X]/59.1mL HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED; 12 [hp_X]/59.1mL HYPERICUM PERFORATUM WHOLE; 30 [hp_X]/59.1mL MEASLES VIRUS; 4 [hp_X]/59.1mL MYRRH; 4 [hp_X]/59.1mL PEUMUS BOLDUS LEAF; 12 [hp_X]/59.1mL PHOSPHORUS; 4 [hp_X]/59.1mL PLANTAGO MAJOR; 9 [hp_X]/59.1mL PORK LIVER; 30 [hp_X]/59.1mL RANCID BEEF; 9 [hp_X]/59.1mL RHODODENDRON TOMENTOSUM LEAFY TWIG; 4 [hp_X]/59.1mL SOLIDAGO VIRGAUREA FLOWERING TOP; 9 [hp_X]/59.1mL SUS SCROFA ADRENAL GLAND; 9 [hp_X]/59.1mL SUS SCROFA PANCREAS
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Allergens [CS]; Allergens [CS]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Dietary Proteins [CS]; Food Additives [CS]; Fungal Proteins [CS]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Fungal Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Plant Proteins [CS]; Plant 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:1/1/2019

Package Information

No. Package Code Package Description Billing Unit
164578-0158-159.1 mL in 1 BOTTLE (64578-0158-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC64578-0158The 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 NAMEBacteria-ChordThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAzadirachta, Belladonna, Berber vulg, Boldo, Candida alb, Ceanothus, Cetraria, Crotalus hor , Echinacea, Glandula suprarenalis suis, Glycyrrhiza, Hamamelis, Hepar suis, Hydrastis, Hydrocotyle, Hypericum, Lappa, Ledum, Millefolium, Morbillinum, Myrrha, Pancreas, Pertussinum, Phos, Plantago, Pyrogenium, Solidago, ZingiberThe 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 DATE1/1/2019This 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 NAMEACHILLEA MILLEFOLIUM WHOLE; ARCTIUM LAPPA ROOT; ATROPA BELLADONNA; AZADIRACHTA INDICA BARK; BERBERIS VULGARIS ROOT BARK; CANDIDA ALBICANS; CEANOTHUS AMERICANUS LEAF; CENTELLA ASIATICA; CETRARIA ISLANDICA WHOLE; CROTALUS HORRIDUS HORRIDUS VENOM; ECHINACEA, UNSPECIFIED; GINGER; GLYCYRRHIZA GLABRA; GOLDENSEAL; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED; HYPERICUM PERFORATUM WHOLE; MEASLES VIRUS; MYRRH; PEUMUS BOLDUS LEAF; PHOSPHORUS; PLANTAGO MAJOR; PORK LIVER; RANCID BEEF; RHODODENDRON TOMENTOSUM LEAFY TWIG; SOLIDAGO VIRGAUREA FLOWERING TOP; SUS SCROFA ADRENAL GLAND; SUS SCROFA PANCREASAn 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 STRENGTH12; 4; 8; 8; 9; 30; 4; 6; 12; 12; 4; 6; 4; 5; 6; 30; 12; 30; 4; 4; 12; 4; 9; 30; 9; 4; 9; 9 
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; [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], Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Dietary Proteins [CS], Food Additives [CS], Fungal Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Plant 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