64578-0061 NDC - COLO-CHORD (HOMEOPATHIC LIQUID)

Drug Information

Product NDC: 64578-0061

Proprietary Name: Colo-Chord

Non Proprietary Name: Homeopathic Liquid

Active Ingredient(s):
  • 12 [hp_X]/59.1mL ABELMOSCHUS MOSCHATUS SEED;
  • 15 [hp_X]/59.1mL ACTIVATED CHARCOAL;
  • 12 [hp_X]/59.1mL ARANEUS DIADEMATUS;
  • 12 [hp_X]/59.1mL ASAFETIDA;
  • 30 [hp_X]/59.1mL BAPTISIA TINCTORIA ROOT;
  • 4 [hp_X]/59.1mL BERBERIS VULGARIS ROOT BARK;
  • 8 [hp_X]/59.1mL BOS TAURUS BILE;
  • 8 [hp_X]/59.1mL BOS TAURUS COLOSTRUM;
  • 18 [hp_X]/59.1mL CANDIDA ALBICANS;
  • 12 [hp_X]/59.1mL COW MILK;
  • 24 [hp_C]/59.1mL ESCHERICHIA COLI;
  • 4 [hp_X]/59.1mL FRANGULA PURSHIANA BARK;
  • 12 [hp_X]/59.1mL LYCOPODIUM CLAVATUM SPORE;
  • 12 [hp_X]/59.1mL MANDRAGORA OFFICINARUM ROOT;
  • 12 [hp_X]/59.1mL MARSDENIA CONDURANGO BARK;
  • 12 [hp_X]/59.1mL MERCURIUS SOLUBILIS;
  • 9 [hp_X]/59.1mL PORK LIVER;
  • 4 [hp_X]/59.1mL RHEUM OFFICINALE ROOT;
  • 15 [hp_X]/59.1mL SELENIUM;
  • 9 [hp_X]/59.1mL SUS SCROFA NASAL MUCOSA;
  • 12 [hp_X]/59.1mL VERATRUM ALBUM ROOT


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Allergens [CS];
  • Allergens [CS];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Dietary Proteins [CS];
  • Fungal Proteins [CS];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased IgG Production [PE];
  • Milk Proteins [CS];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Non-Standardized Fungal Allergenic Extract [EPC]

Labeler Information

Labeler Name: Energetix Corp
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:10/8/2014

Package Information

No. Package Code Package Description Billing Unit
164578-0061-159.1 mL in 1 BOTTLE, DROPPER (64578-0061-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC64578-0061The 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 NAMEColo-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 NAMEHomeopathic LiquidThe 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 DATE10/8/2014This 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 CorpName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEABELMOSCHUS MOSCHATUS SEED; ACTIVATED CHARCOAL; ARANEUS DIADEMATUS; ASAFETIDA; BAPTISIA TINCTORIA ROOT; BERBERIS VULGARIS ROOT BARK; BOS TAURUS BILE; BOS TAURUS COLOSTRUM; CANDIDA ALBICANS; COW MILK; ESCHERICHIA COLI; FRANGULA PURSHIANA BARK; LYCOPODIUM CLAVATUM SPORE; MANDRAGORA OFFICINARUM ROOT; MARSDENIA CONDURANGO BARK; MERCURIUS SOLUBILIS; PORK LIVER; RHEUM OFFICINALE ROOT; SELENIUM; SUS SCROFA NASAL MUCOSA; VERATRUM ALBUM ROOTAn 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; 15; 12; 12; 30; 4; 8; 8; 18; 12; 24; 4; 12; 12; 12; 12; 9; 4; 15; 9; 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_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 
PHARM CLASSESAllergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Fungal Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Milk Proteins [CS], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC] 

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This page was last updated on: 2/1/2023