60295-5302 NDC - POTENTILLA ANSERINA, AESCULUS HIPPOCASTANUM, USTILAGO MAIDIS, SECALE CORNUTUM, RUTA GRAVEOLENS

Drug Information

  • Product NDC: 60295-5302
  • Proprietary Name:
  • Non Proprietary Name: Potentilla Anserina, Aesculus Hippocastanum, Ustilago Maidis, Secale Cornutum, Ruta Graveolens
  • Active Ingredient(s): 1 [hp_X]/100mL ARGENTINA ANSERINA FLOWERING TOP; 4 [hp_X]/100mL CLAVICEPS PURPUREA SCLEROTIUM; 1 [hp_X]/100mL HORSE CHESTNUT; 3 [hp_X]/100mL RUTA GRAVEOLENS WHOLE; 5 [hp_X]/100mL USTILAGO MAYDIS
  • 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:3/1/1992

Package Information

No. Package Code Package Description Billing Unit
160295-5302-130000 mL in 1 CONTAINER (60295-5302-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC60295-5302The 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 NAMEPotentilla Anserina, Aesculus Hippocastanum, Ustilago Maidis, Secale Cornutum, Ruta GraveolensThe 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 DATE3/1/1992This 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 NAMEARGENTINA ANSERINA FLOWERING TOP; CLAVICEPS PURPUREA SCLEROTIUM; HORSE CHESTNUT; RUTA GRAVEOLENS WHOLE; USTILAGO MAYDISAn 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; 4; 1; 3; 5 
ACTIVE INGRED UNIT[hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL 

Download Record

Download this NDC record record in Text format: Export

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

Download this NDC record record in XML format: Export

This page was last updated on: 11/21/2025

Previous Code
Next Code