64578-0151 NDC - TOX-CHORD (ALFALFA, ALUMINA, BENZOICUM AC, CARBONEUM, CETRARIA, FOLLICULINUM, FUCUS, FUMARICUM AC, HEPAR SUIS, KALI CARB, KREOSOTUM, NAT MUR, PARAFFINUM, PETROLEUM, PHOSPHORICUM AC, PHOS, PIX LIQUIDA, PLANTAGO, PLUMB MET, PULSATILLA, RADIUM BROM, RESORCINUM, SALOL, SILICEA, SYMPHYTUM, TABACUM, TEREBINTHINA, THYROIDINUM, TRITICUM, ZINC OXYD.)

Drug Information

  • Product NDC: 64578-0151
  • Proprietary Name: Tox-Chord
  • Non Proprietary Name: Alfalfa, Alumina, Benzoicum ac, Carboneum, Cetraria, Folliculinum, Fucus, Fumaricum ac, Hepar suis, Kali carb, Kreosotum, Nat mur, Paraffinum, Petroleum, Phosphoricum ac, Phos, Pix liquida, Plantago, Plumb met, Pulsatilla, Radium brom, Resorcinum, Salol, Silicea, Symphytum, Tabacum, Terebinthina, Thyroidinum, Triticum, Zinc oxyd.
  • Active Ingredient(s): 4 [hp_X]/59.1mL ALFALFA; 18 [hp_X]/59.1mL ALUMINUM OXIDE; 18 [hp_X]/59.1mL BENZOIC ACID; 9 [hp_C]/59.1mL CETRARIA ISLANDICA SUBSP. ISLANDICA; 6 [hp_X]/59.1mL COMFREY ROOT; 18 [hp_X]/59.1mL D&C BLACK NO. 2; 4 [hp_X]/59.1mL ELYMUS REPENS ROOT; 18 [hp_X]/59.1mL ESTRONE; 5 [hp_X]/59.1mL FUCUS VESICULOSUS; 18 [hp_X]/59.1mL FUMARIC ACID; 18 [hp_X]/59.1mL KEROSENE; 15 [hp_X]/59.1mL LEAD; 18 [hp_X]/59.1mL PARAFFIN; 18 [hp_X]/59.1mL PHENYL SALICYLATE; 12 [hp_X]/59.1mL PHOSPHORIC ACID; 12 [hp_X]/59.1mL PHOSPHORUS; 18 [hp_X]/59.1mL PINE TAR; 4 [hp_X]/59.1mL PLANTAGO MAJOR; 9 [hp_X]/59.1mL PORK LIVER; 12 [hp_X]/59.1mL POTASSIUM CARBONATE; 12 [hp_X]/59.1mL PULSATILLA VULGARIS; 15 [hp_C]/59.1mL RADIUM BROMIDE; 18 [hp_X]/59.1mL RESORCINOL; 12 [hp_X]/59.1mL SILICON DIOXIDE; 12 [hp_X]/59.1mL SODIUM CHLORIDE; 9 [hp_X]/59.1mL THYROID, UNSPECIFIED; 30 [hp_X]/59.1mL TOBACCO LEAF; 18 [hp_X]/59.1mL TURPENTINE OIL; 18 [hp_X]/59.1mL WOOD CREOSOTE; 18 [hp_X]/59.1mL ZINC OXIDE
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Ammonium Ion Binding Activity [MoA]; Cell-mediated Immunity [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Nitrogen Binding Agent [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; 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:4/1/2017

Package Information

No. Package Code Package Description Billing Unit
164578-0151-159.1 mL in 1 BOTTLE, DROPPER (64578-0151-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC64578-0151The 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 NAMETox-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 NAMEAlfalfa, Alumina, Benzoicum ac, Carboneum, Cetraria, Folliculinum, Fucus, Fumaricum ac, Hepar suis, Kali carb, Kreosotum, Nat mur, Paraffinum, Petroleum, Phosphoricum ac, Phos, Pix liquida, Plantago, Plumb met, Pulsatilla, Radium brom, Resorcinum, Salol, Silicea, Symphytum, Tabacum, Terebinthina, Thyroidinum, Triticum, Zinc oxyd.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 DATE4/1/2017This 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 NAMEALFALFA; ALUMINUM OXIDE; BENZOIC ACID; CETRARIA ISLANDICA SUBSP. ISLANDICA; COMFREY ROOT; D&C BLACK NO. 2; ELYMUS REPENS ROOT; ESTRONE; FUCUS VESICULOSUS; FUMARIC ACID; KEROSENE; LEAD; PARAFFIN; PHENYL SALICYLATE; PHOSPHORIC ACID; PHOSPHORUS; PINE TAR; PLANTAGO MAJOR; PORK LIVER; POTASSIUM CARBONATE; PULSATILLA VULGARIS; RADIUM BROMIDE; RESORCINOL; SILICON DIOXIDE; SODIUM CHLORIDE; THYROID, UNSPECIFIED; TOBACCO LEAF; TURPENTINE OIL; WOOD CREOSOTE; ZINC OXIDEAn 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 STRENGTH4; 18; 18; 9; 6; 18; 4; 18; 5; 18; 18; 15; 18; 18; 12; 12; 18; 4; 9; 12; 12; 15; 18; 12; 12; 9; 30; 18; 18; 18 
ACTIVE INGRED UNIT[hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_C]/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_C]/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], Ammonium Ion Binding Activity [MoA], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Nitrogen Binding Agent [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS] 

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

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