64578-0075 NDC - RENA-CHORD (HOMEOPATHIC LIQUID)

Drug Information

Product NDC: 64578-0075

Proprietary Name: Rena-Chord

Non Proprietary Name: Homeopathic Liquid

Active Ingredient(s):
  • 6 [hp_X]/59.1mL AGATHOSMA BETULINA LEAF;
  • 15 [hp_X]/59.1mL ALUMINUM OXIDE;
  • 15 [hp_X]/59.1mL ANTIMONY;
  • 12 [hp_X]/59.1mL APIS MELLIFERA;
  • 5 [hp_X]/59.1mL ARCTOSTAPHYLOS UVA-URSI LEAF;
  • 15 [hp_X]/59.1mL ARSENIC;
  • 4 [hp_X]/59.1mL BERBERIS VULGARIS ROOT BARK;
  • 12 [hp_X]/59.1mL BRYONIA ALBA ROOT;
  • 15 [hp_X]/59.1mL CADMIUM;
  • 15 [hp_X]/59.1mL COBALT;
  • 15 [hp_X]/59.1mL COPPER;
  • 4 [hp_X]/59.1mL ECHINACEA ANGUSTIFOLIA;
  • 4 [hp_X]/59.1mL ELYMUS REPENS ROOT;
  • 6 [hp_X]/59.1mL EUTROCHIUM PURPUREUM ROOT;
  • 15 [hp_X]/59.1mL IRON;
  • 15 [hp_X]/59.1mL KEROSENE;
  • 15 [hp_X]/59.1mL LEAD;
  • 15 [hp_X]/59.1mL LITHIUM CARBONATE;
  • 8 [hp_X]/59.1mL LYTTA VESICATORIA;
  • 15 [hp_X]/59.1mL MERCURIC CHLORIDE;
  • 15 [hp_X]/59.1mL PLATINUM;
  • 12 [hp_X]/59.1mL PULSATILLA VULGARIS;
  • 5 [hp_X]/59.1mL SARSAPARILLA;
  • 8 [hp_X]/59.1mL SAW PALMETTO;
  • 6 [hp_X]/59.1mL SOLIDAGO VIRGAUREA FLOWERING TOP;
  • 4 [hp_X]/59.1mL TARAXACUM OFFICINALE;
  • 12 [hp_X]/59.1mL THUJA OCCIDENTALIS LEAFY TWIG;
  • 15 [hp_X]/59.1mL TITANIUM;
  • 15 [hp_X]/59.1mL VANADIUM;
  • 15 [hp_X]/59.1mL ZINC


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Allergens [CS];
  • Allergens [CS];
  • Bee Venoms [CS];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Copper [CS];
  • Copper-containing Intrauterine Device [EPC];
  • Decreased Embryonic Implantation [PE];
  • Decreased Sperm Motility [PE];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased IgG Production [PE];
  • Inhibit Ovum Fertilization [PE];
  • Mood Stabilizer [EPC];
  • Standardized Chemical Allergen [EPC];
  • Standardized Insect Venom Allergenic Extract [EPC]

Labeler Information

Labeler Name: Energetix Corp
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:4/28/2016

Package Information

No. Package Code Package Description Billing Unit
164578-0075-159.1 mL in 1 BOTTLE, DROPPER (64578-0075-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC64578-0075The 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 NAMERena-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 DATE4/28/2016This 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 CorpName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEAGATHOSMA BETULINA LEAF; ALUMINUM OXIDE; ANTIMONY; APIS MELLIFERA; ARCTOSTAPHYLOS UVA-URSI LEAF; ARSENIC; BERBERIS VULGARIS ROOT BARK; BRYONIA ALBA ROOT; CADMIUM; COBALT; COPPER; ECHINACEA ANGUSTIFOLIA; ELYMUS REPENS ROOT; EUTROCHIUM PURPUREUM ROOT; IRON; KEROSENE; LEAD; LITHIUM CARBONATE; LYTTA VESICATORIA; MERCURIC CHLORIDE; PLATINUM; PULSATILLA VULGARIS; SARSAPARILLA; SAW PALMETTO; SOLIDAGO VIRGAUREA FLOWERING TOP; TARAXACUM OFFICINALE; THUJA OCCIDENTALIS LEAFY TWIG; TITANIUM; VANADIUM; ZINCAn 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 STRENGTH6; 15; 15; 12; 5; 15; 4; 12; 15; 15; 15; 4; 4; 6; 15; 15; 15; 15; 8; 15; 15; 12; 5; 8; 6; 4; 12; 15; 15; 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_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], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Inhibit Ovum Fertilization [PE], Mood Stabilizer [EPC], Standardized Chemical Allergen [EPC], Standardized Insect Venom Allergenic Extract [EPC] 

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