64578-0062 NDC - DENTAL-CHORD (HOMEOPATHIC LIQUID)

Drug Information

Product NDC: 64578-0062

Proprietary Name: Dental-Chord

Non Proprietary Name: Homeopathic Liquid

Active Ingredient(s):
  • 15 [hp_X]/59.1mL ACETIC ACID;
  • 15 [hp_X]/59.1mL AMMONIUM CHLORIDE;
  • 4 [hp_X]/59.1mL ARCTIUM LAPPA ROOT;
  • 12 [hp_X]/59.1mL CALCIUM FLUORIDE;
  • 15 [hp_X]/59.1mL COPPER;
  • 6 [hp_X]/59.1mL DELPHINIUM STAPHISAGRIA SEED;
  • 4 [hp_X]/59.1mL GLYCYRRHIZA GLABRA;
  • 15 [hp_X]/59.1mL GOLD;
  • 12 [hp_X]/59.1mL IRON;
  • 30 [hp_C]/59.1mL LACTOSE, X-RAY EXPOSED (1000 RAD);
  • 12 [hp_X]/59.1mL LEMON JUICE;
  • 12 [hp_X]/59.1mL MERCURIUS SOLUBILIS;
  • 6 [hp_X]/59.1mL MYRRH;
  • 15 [hp_X]/59.1mL PALLADIUM;
  • 15 [hp_X]/59.1mL PHENOL;
  • 15 [hp_X]/59.1mL PHOSPHORIC ACID;
  • 4 [hp_X]/59.1mL PHYTOLACCA AMERICANA ROOT;
  • 15 [hp_X]/59.1mL SELENIUM;
  • 12 [hp_X]/59.1mL SILICON DIOXIDE;
  • 15 [hp_X]/59.1mL SILVER;
  • 12 [hp_X]/59.1mL SODIUM FLUORIDE;
  • 4 [hp_X]/59.1mL STILLINGIA SYLVATICA ROOT;
  • 9 [hp_X]/59.1mL SUS SCROFA BONE MARROW;
  • 15 [hp_X]/59.1mL TIN;
  • 12 [hp_X]/59.1mL TRIBASIC CALCIUM PHOSPHATE;
  • 4 [hp_X]/59.1mL TRIFOLIUM PRATENSE FLOWER;
  • 15 [hp_X]/59.1mL ZINC OXIDE


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Allergens [CS];
  • Allergens [CS];
  • Blood Coagulation Factor [EPC];
  • Calcium [CS];
  • Cations;
  • Divalent [CS];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Copper Absorption Inhibitor [EPC];
  • Copper [CS];
  • Copper-containing Intrauterine Device [EPC];
  • Decreased Copper Ion Absorption [PE];
  • Decreased Embryonic Implantation [PE];
  • Decreased Sperm Motility [PE];
  • Dietary Proteins [CS];
  • Increased Coagulation Factor Activity [PE];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Inhibit Ovum Fertilization [PE];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Non-Standardized Plant Allergenic Extract [EPC];
  • Plant Proteins [CS];
  • Standardized Chemical Allergen [EPC]

Labeler Information

Labeler Name: Energetix Corp
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:9/4/2014

Package Information

No. Package Code Package Description Billing Unit
164578-0062-159.1 mL in 1 BOTTLE, DROPPER (64578-0062-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC64578-0062The 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 NAMEDental-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 DATE9/4/2014This 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 NAMEACETIC ACID; AMMONIUM CHLORIDE; ARCTIUM LAPPA ROOT; CALCIUM FLUORIDE; COPPER; DELPHINIUM STAPHISAGRIA SEED; GLYCYRRHIZA GLABRA; GOLD; IRON; LACTOSE, X-RAY EXPOSED (1000 RAD); LEMON JUICE; MERCURIUS SOLUBILIS; MYRRH; PALLADIUM; PHENOL; PHOSPHORIC ACID; PHYTOLACCA AMERICANA ROOT; SELENIUM; SILICON DIOXIDE; SILVER; SODIUM FLUORIDE; STILLINGIA SYLVATICA ROOT; SUS SCROFA BONE MARROW; TIN; TRIBASIC CALCIUM PHOSPHATE; TRIFOLIUM PRATENSE FLOWER; 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 STRENGTH15; 15; 4; 12; 15; 6; 4; 15; 12; 30; 12; 12; 6; 15; 15; 15; 4; 15; 12; 15; 12; 4; 9; 15; 12; 4; 15 
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_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 
PHARM CLASSESAllergens [CS], Allergens [CS], Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Copper Absorption Inhibitor [EPC], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Copper Ion Absorption [PE], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Dietary Proteins [CS], Increased Coagulation Factor Activity [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Inhibit Ovum Fertilization [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Standardized Chemical Allergen [EPC] 

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