60295-5304 NDC - POLYGONUM AVICULARE, ACORUS CALAMUS, RHUS TOXICODENDRON, GNAPHALIUM POLYCEPHALUM, RHODODENDRON CHRYSANTHUM, COLOCYNTHIS, COLCHICUM AUTUMNALE, KALI IODATUM, ICHTHYOLUM, SYMPHYTUM OFFICINALE

Drug Information

  • Product NDC: 60295-5304
  • Proprietary Name:
  • Non Proprietary Name: Polygonum Aviculare, Acorus Calamus, Rhus Toxicodendron, Gnaphalium Polycephalum, Rhododendron Chrysanthum, Colocynthis, Colchicum Autumnale, Kali Iodatum, Ichthyolum, Symphytum Officinale
  • Active Ingredient(s): 1 [hp_X]/100mL ACORUS CALAMUS WHOLE; 3 [hp_X]/100mL CITRULLUS COLOCYNTHIS FRUIT PULP; 3 [hp_X]/100mL COLCHICUM AUTUMNALE BULB; 6 [hp_X]/100mL COMFREY ROOT; 3 [hp_X]/100mL ICHTHAMMOL; 1 [hp_X]/100mL POLYGONUM AVICULARE TOP; 4 [hp_X]/100mL POTASSIUM IODIDE; 2 [hp_X]/100mL PSEUDOGNAPHALIUM OBTUSIFOLIUM; 3 [hp_X]/100mL RHODODENDRON AUREUM LEAF; 4 [hp_X]/100mL TOXICODENDRON PUBESCENS LEAF
  • Administration Route(s):
  • Dosage Form(s): LIQUID

Labeler Information

Field Name Field Value
Labeler Name: Nestmann Pharma GmbH
Product Type: DRUG FOR FURTHER PROCESSING
FDA Application Number:
Marketing Category: DRUG FOR FURTHER PROCESSING
Start Marketing Date:6/14/2022

Package Information

No. Package Code Package Description Billing Unit
160295-5304-130000 mL in 1 CONTAINER (60295-5304-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC60295-5304The 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 NAMEDRUG FOR FURTHER PROCESSINGIndicates 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.
NON PROPRIETARY NAMEPolygonum Aviculare, Acorus Calamus, Rhus Toxicodendron, Gnaphalium Polycephalum, Rhododendron Chrysanthum, Colocynthis, Colchicum Autumnale, Kali Iodatum, Ichthyolum, Symphytum 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.
START MARKETING DATE6/14/2022This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEDRUG FOR FURTHER PROCESSINGProduct 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 NAMENestmann Pharma GmbHName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACORUS CALAMUS WHOLE; CITRULLUS COLOCYNTHIS FRUIT PULP; COLCHICUM AUTUMNALE BULB; COMFREY ROOT; ICHTHAMMOL; POLYGONUM AVICULARE TOP; POTASSIUM IODIDE; PSEUDOGNAPHALIUM OBTUSIFOLIUM; RHODODENDRON AUREUM LEAF; TOXICODENDRON PUBESCENS LEAFAn 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 STRENGTH1; 3; 3; 6; 3; 1; 4; 2; 3; 4 
ACTIVE INGRED UNIT[hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL 

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This page was last updated on: 12/6/2025

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