64578-0103 NDC - RENAPATH (BENZOICUM ACIDUM, BERBERIS VULGARIS, BRYONIA, DNA, EUPATORIUM PURPUREUM, GLANDULA SUPRARENALIS SUIS, HYDRANGEA ARBORESCENS, HYPOTHALAMUS, MERCURIUS CORROSIVUS, PANCREAS SUIS, PAREIRA BRAVA, PETROSELINUM SATIVUM, PITUITARUM POSTERIUM, RUBIA TINCTORUM, SARSAPARILLA, SOLIDAGO VIRGAUREA, THYROIDINUM (BOVINE), UVA-URSI)

Drug Information

Product NDC: 64578-0103

Proprietary Name: Renapath

Non Proprietary Name: Benzoicum Acidum, Berberis Vulgaris, Bryonia, DNA, Eupatorium Purpureum, Glandula Suprarenalis Suis, Hydrangea Arborescens, Hypothalamus, Mercurius Corrosivus, Pancreas Suis, Pareira Brava, Petroselinum Sativum, Pituitarum Posterium, Rubia Tinctorum, Sarsaparilla, Solidago Virgaurea, Thyroidinum (Bovine), Uva-Ursi

Active Ingredient(s):
  • 4 [hp_X]/mL ARCTOSTAPHYLOS UVA-URSI LEAF;
  • 10 [hp_X]/mL BENZOIC ACID;
  • 4 [hp_X]/mL BERBERIS VULGARIS ROOT BARK;
  • 12 [hp_X]/mL BOS TAURUS HYPOTHALAMUS;
  • 12 [hp_X]/mL BRYONIA ALBA ROOT;
  • 10 [hp_X]/mL CHONDRODENDRON TOMENTOSUM ROOT;
  • 12 [hp_X]/mL EUTROCHIUM PURPUREUM ROOT;
  • 12 [hp_X]/mL HERRING SPERM DNA;
  • 4 [hp_X]/mL HYDRANGEA ARBORESCENS ROOT;
  • 12 [hp_X]/mL MERCURIC CHLORIDE;
  • 4 [hp_X]/mL PETROSELINUM CRISPUM;
  • 6 [hp_X]/mL RUBIA TINCTORUM ROOT;
  • 4 [hp_X]/mL SARSAPARILLA;
  • 4 [hp_X]/mL SOLIDAGO VIRGAUREA FLOWERING TOP;
  • 9 [hp_X]/mL SUS SCROFA ADRENAL GLAND;
  • 9 [hp_X]/mL SUS SCROFA PANCREAS;
  • 12 [hp_X]/mL SUS SCROFA PITUITARY GLAND;
  • 9 [hp_X]/mL THYROID, BOVINE


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Ammonium Ion Binding Activity [MoA];
  • Nitrogen Binding Agent [EPC]

Labeler Information

Labeler Name: Energetix Corp
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:6/6/2014

Package Information

No. Package Code Package Description Billing Unit
164578-0103-159.1 mL in 1 BOTTLE, DROPPER (64578-0103-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC64578-0103The 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 NAMERenapathThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEBenzoicum Acidum, Berberis Vulgaris, Bryonia, DNA, Eupatorium Purpureum, Glandula Suprarenalis Suis, Hydrangea Arborescens, Hypothalamus, Mercurius Corrosivus, Pancreas Suis, Pareira Brava, Petroselinum Sativum, Pituitarum Posterium, Rubia Tinctorum, Sarsaparilla, Solidago Virgaurea, Thyroidinum (Bovine), Uva-UrsiThe 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 DATE6/6/2014This 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 NAMEARCTOSTAPHYLOS UVA-URSI LEAF; BENZOIC ACID; BERBERIS VULGARIS ROOT BARK; BOS TAURUS HYPOTHALAMUS; BRYONIA ALBA ROOT; CHONDRODENDRON TOMENTOSUM ROOT; EUTROCHIUM PURPUREUM ROOT; HERRING SPERM DNA; HYDRANGEA ARBORESCENS ROOT; MERCURIC CHLORIDE; PETROSELINUM CRISPUM; RUBIA TINCTORUM ROOT; SARSAPARILLA; SOLIDAGO VIRGAUREA FLOWERING TOP; SUS SCROFA ADRENAL GLAND; SUS SCROFA PANCREAS; SUS SCROFA PITUITARY GLAND; THYROID, BOVINEAn 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; 10; 4; 12; 12; 10; 12; 12; 4; 12; 4; 6; 4; 4; 9; 9; 12; 9 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESAmmonium Ion Binding Activity [MoA], Nitrogen Binding Agent [EPC] 

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