83027-0100 NDC - RENAL SARCODE (RUBIA TINCTORUM, URTICA DIOICA, SARSAPARILLA (SMILAX REGELII), BERBERIS VULGARIS, COCCUS CACTI, BENZOICUM ACIDUM, KIDNEY (BOVINE), LITHIUM CARBONICUM, LYCOPODIUM CLAVATUM, PETROSELINUM SATIVUM, TARAXACUM OFFICINALE, COLOCYNTHIS, ATROPINUM SULPHURICUM, CALCAREA CARBONICA, HYDRANGEA ARBORESCENS)

Drug Information

  • Product NDC: 83027-0100
  • Proprietary Name: Renal Sarcode
  • Non Proprietary Name: Rubia Tinctorum, Urtica Dioica, Sarsaparilla (smilax Regelii), Berberis Vulgaris, Coccus Cacti, Benzoicum Acidum, Kidney (Bovine), Lithium Carbonicum, Lycopodium Clavatum, Petroselinum Sativum, Taraxacum Officinale, Colocynthis, Atropinum Sulphuricum, Calcarea Carbonica, Hydrangea Arborescens
  • Active Ingredient(s): 10 [hp_X]/mL ATROPINE SULFATE; 6 [hp_X]/mL BEEF KIDNEY; 6 [hp_X]/mL BENZOIC ACID; 5 [hp_X]/mL BERBERIS VULGARIS ROOT BARK; 7 [hp_X]/mL CITRULLUS COLOCYNTHIS FRUIT PULP; 12 [hp_X]/mL HYDRANGEA ARBORESCENS ROOT; 6 [hp_X]/mL LITHIUM CARBONATE; 6 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE; 12 [hp_X]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE; 6 [hp_X]/mL PETROSELINUM CRISPUM WHOLE; 5 [hp_X]/mL PROTORTONIA CACTI; 3 [hp_X]/mL RUBIA TINCTORUM ROOT; 4 [hp_X]/mL SMILAX ORNATA ROOT; 6 [hp_X]/mL TARAXACUM OFFICINALE; 3 [hp_X]/mL URTICA DIOICA WHOLE
  • Administration Route(s): ORAL
  • Dosage Form(s): SPRAY
  • Pharmacy Class(es): Ammonium Ion Binding Activity [MoA]; Anticholinergic [EPC]; Cholinergic Antagonists [MoA]; Cholinergic Muscarinic Antagonist [EPC]; Cholinergic Muscarinic Antagonists [MoA]; Mood Stabilizer [EPC]; Nitrogen Binding Agent [EPC]

Labeler Information

Field Name Field Value
Labeler Name: Nutritional Specialties, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:8/11/2023

Package Information

No. Package Code Package Description Billing Unit
183027-0100-160 mL in 1 BOTTLE, SPRAY (83027-0100-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC83027-0100The 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 NAMERenal SarcodeThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMERubia Tinctorum, Urtica Dioica, Sarsaparilla (smilax Regelii), Berberis Vulgaris, Coccus Cacti, Benzoicum Acidum, Kidney (Bovine), Lithium Carbonicum, Lycopodium Clavatum, Petroselinum Sativum, Taraxacum Officinale, Colocynthis, Atropinum Sulphuricum, Calcarea Carbonica, Hydrangea ArborescensThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESPRAYThe 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 DATE8/11/2023This 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 NAMENutritional Specialties, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEATROPINE SULFATE; BEEF KIDNEY; BENZOIC ACID; BERBERIS VULGARIS ROOT BARK; CITRULLUS COLOCYNTHIS FRUIT PULP; HYDRANGEA ARBORESCENS ROOT; LITHIUM CARBONATE; LYCOPODIUM CLAVATUM SPORE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PETROSELINUM CRISPUM WHOLE; PROTORTONIA CACTI; RUBIA TINCTORUM ROOT; SMILAX ORNATA ROOT; TARAXACUM OFFICINALE; URTICA DIOICA WHOLEAn 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 STRENGTH10; 6; 6; 5; 7; 12; 6; 6; 12; 6; 5; 3; 4; 6; 3 
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 
PHARM CLASSESAmmonium Ion Binding Activity [MoA], Anticholinergic [EPC], Cholinergic Antagonists [MoA], Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA], Mood Stabilizer [EPC], Nitrogen Binding Agent [EPC] 

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This page was last updated on: 7/4/2025

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