62106-3126 NDC - DROSERA PLEX (COUGH SYRUP)

Drug Information

Product NDC: 62106-3126

Proprietary Name: Drosera Plex

Non Proprietary Name: Cough Syrup

Active Ingredient(s):
  • 3 [hp_X]/180mL DROSERA ROTUNDIFOLIA;
  • 10 [hp_X]/180mL HYOSCYAMUS NIGER;
  • 6 [hp_X]/180mL IPECAC;
  • 10 [hp_X]/180mL LACHESIS MUTA VENOM;
  • 7 [hp_X]/180mL OREGANO FLOWERING TOP;
  • 5 [hp_X]/180mL PAPAVER RHOEAS FLOWER;
  • 8 [hp_X]/180mL PULSATILLA PRATENSIS;
  • 10 [hp_X]/180mL RUMEX CRISPUS ROOT;
  • 10 [hp_X]/180mL SPONGIA OFFICINALIS SKELETON, ROASTED;
  • 8 [hp_X]/180mL SULFUR


Administration Route(s): ORAL

Dosage Form(s): SYRUP

Labeler Information

Labeler Name: Seroyal USA
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:9/6/2017

Package Information

No. Package Code Package Description Billing Unit
162106-3126-11 BOTTLE, GLASS in 1 CARTON (62106-3126-1) / 180 mL in 1 BOTTLE, GLASS

NDC Record

Field Name Field Value Definition
PRODUCT NDC62106-3126The 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 NAMEDrosera 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 NAMECough SyrupThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESYRUPThe 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 DATE9/6/2017This 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 NAMEDROSERA ROTUNDIFOLIA; HYOSCYAMUS NIGER; IPECAC; LACHESIS MUTA VENOM; OREGANO FLOWERING TOP; PAPAVER RHOEAS FLOWER; PULSATILLA PRATENSIS; RUMEX CRISPUS ROOT; SPONGIA OFFICINALIS SKELETON, ROASTED; SULFURAn 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 STRENGTH3; 10; 6; 10; 7; 5; 8; 10; 10; 8 
ACTIVE INGRED UNIT[hp_X]/180mL; [hp_X]/180mL; [hp_X]/180mL; [hp_X]/180mL; [hp_X]/180mL; [hp_X]/180mL; [hp_X]/180mL; [hp_X]/180mL; [hp_X]/180mL; [hp_X]/180mL 

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This page was last updated on: 4/12/2024