62106-1200 NDC - CARDUUS PLEX (BELLADONNA, CARDUUS MARIANUS, CHELIDONIUM MAJUS, CHOLESTERINUM, CINCHONA SUCCIRUBRA, COLOCYNTHIS, LEPTANDRA VIRGINICA, LYCOPODIUM CLAVATUM, PODOPHYLLUM PELTATUM, TARAXACUM OFFICINALE)

Drug Information

Product NDC: 62106-1200

Proprietary Name: CARDUUS PLEX

Non Proprietary Name: belladonna, carduus marianus, chelidonium majus, cholesterinum, cinchona succirubra, colocynthis, leptandra virginica, lycopodium clavatum, podophyllum peltatum, taraxacum officinale

Active Ingredient(s):
  • 4 [hp_X]/30mL ATROPA BELLADONNA;
  • 2 [hp_X]/30mL CHELIDONIUM MAJUS;
  • 4 [hp_X]/30mL CHOLESTEROL;
  • 3 [hp_X]/30mL CINCHONA PUBESCENS BARK;
  • 6 [hp_X]/30mL CITRULLUS COLOCYNTHIS FRUIT PULP;
  • 1 [hp_X]/30mL CULVER'S ROOT;
  • 4 [hp_X]/30mL LYCOPODIUM CLAVATUM SPORE;
  • 2 [hp_X]/30mL MILK THISTLE;
  • 4 [hp_X]/30mL PODOPHYLLUM PELTATUM ROOT;
  • 2 [hp_X]/30mL TARAXACUM OFFICINALE


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Labeler Information

Labeler Name: Seroyal USA
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:5/18/2016

Package Information

No. Package Code Package Description Billing Unit
162106-1200-01 BOTTLE, GLASS in 1 CARTON (62106-1200-0) / 30 mL in 1 BOTTLE, GLASS

NDC Record

Field Name Field Value Definition
PRODUCT NDC62106-1200The 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 NAMECARDUUS PLEXThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEbelladonna, carduus marianus, chelidonium majus, cholesterinum, cinchona succirubra, colocynthis, leptandra virginica, lycopodium clavatum, podophyllum peltatum, taraxacum officinaleThe 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 DATE5/18/2016This 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 NAMESeroyal USAName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEATROPA BELLADONNA; CHELIDONIUM MAJUS; CHOLESTEROL; CINCHONA PUBESCENS BARK; CITRULLUS COLOCYNTHIS FRUIT PULP; CULVER'S ROOT; LYCOPODIUM CLAVATUM SPORE; MILK THISTLE; PODOPHYLLUM PELTATUM ROOT; TARAXACUM OFFICINALEAn 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; 2; 4; 3; 6; 1; 4; 2; 4; 2 
ACTIVE INGRED UNIT[hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL 

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

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