60295-0304 NDC - FORMICUM ACIDUM, LACHESIS MUTUS, LUFFA OPERCULATA. PETROLEUM, RHUS TOXICODEBDRON, ARALAI RACEMOSA,GALPHIMIA GLAUCA, THUJA OCCIDENTALIS, URTICA DICICA AND CARDIOSPERMUM

Drug Information

  • Product NDC: 60295-0304
  • Proprietary Name:
  • Non Proprietary Name: Formicum acidum, Lachesis mutus, luffa Operculata. Petroleum, Rhus Toxicodebdron, Aralai racemosa,Galphimia glauca, thuja occidentalis, Urtica dicica and Cardiospermum
  • Active Ingredient(s): 4 [hp_X]/100mL ARALIA RACEMOSA ROOT; 3 [hp_X]/100mL CARDIOSPERMUM HALICACABUM FLOWERING TOP; 12 [hp_X]/100mL FORMIC ACID; 4 [hp_X]/100mL GALPHIMIA GLAUCA FLOWERING TOP; 6 [hp_X]/100mL KEROSENE; 8 [hp_X]/100mL LACHESIS MUTA VENOM; 6 [hp_X]/100mL LUFFA OPERCULATA FRUIT; 4 [hp_X]/100mL THUJA OCCIDENTALIS LEAFY TWIG; 6 [hp_X]/100mL TOXICODENDRON PUBESCENS LEAF; 4 [hp_X]/100mL URTICA DIOICA
  • 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
160295-0304-130000 mL in 1 CONTAINER (60295-0304-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC60295-0304The 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 NAMEFormicum acidum, Lachesis mutus, luffa Operculata. Petroleum, Rhus Toxicodebdron, Aralai racemosa,Galphimia glauca, thuja occidentalis, Urtica dicica and CardiospermumThe 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 NAMEARALIA RACEMOSA ROOT; CARDIOSPERMUM HALICACABUM FLOWERING TOP; FORMIC ACID; GALPHIMIA GLAUCA FLOWERING TOP; KEROSENE; LACHESIS MUTA VENOM; LUFFA OPERCULATA FRUIT; THUJA OCCIDENTALIS LEAFY TWIG; TOXICODENDRON PUBESCENS LEAF; URTICA DIOICAAn 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; 3; 12; 4; 6; 8; 6; 4; 6; 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: 11/21/2025

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