60295-0305 NDC - ECHINACEA AUGUSTIFOLIA, SCROPHULARIA NODOSA, ABROTANUM, PETROLEUM, ALOE SOCOTRINA, MERCURIUS SOLUBILIS, CROTALUS HORIIDUS, THUJA OCCIDENTALIS, LACHESIS MUTUS, ARISTOLOCHIA CLEMATITIS

Drug Information

  • Product NDC: 60295-0305
  • Proprietary Name:
  • Non Proprietary Name: Echinacea augustifolia, Scrophularia nodosa, Abrotanum, Petroleum, Aloe socotrina, Mercurius solubilis, Crotalus horiidus, Thuja occidentalis, Lachesis mutus, Aristolochia clematitis
  • Active Ingredient(s): 1 [hp_X]/100mL ALOE; 6 [hp_X]/100mL ARISTOLOCHIA CLEMATITIS ROOT; 3 [hp_X]/100mL ARTEMISIA ABROTANUM FLOWERING TOP; 10 [hp_X]/100mL CROTALUS HORRIDUS HORRIDUS VENOM; 1 [hp_X]/100mL ECHINACEA ANGUSTIFOLIA; 3 [hp_X]/100mL KEROSENE; 8 [hp_X]/100mL LACHESIS MUTA VENOM; 12 [hp_X]/100mL MERCURIUS SOLUBILIS; 1 [hp_X]/100mL SCROPHULARIA NODOSA; 10 [hp_X]/100mL THUJA OCCIDENTALIS LEAFY TWIG
  • 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
160295-0305-130000 mL in 1 CONTAINER (60295-0305-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC60295-0305The 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 PROCESSINGThe 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.
NON PROPRIETARY NAMEEchinacea augustifolia, Scrophularia nodosa, Abrotanum, Petroleum, Aloe socotrina, Mercurius solubilis, Crotalus horiidus, Thuja occidentalis, Lachesis mutus, Aristolochia clematitisThe 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 PROCESSINGThe translation of the route code submitted by the firm, indicating route of administration.
LABELER NAMENestmann Pharma GmbHThis is the date that the labeler indicates was the start of its marketing of the drug product.
SUBSTANCE NAMEALOE; ARISTOLOCHIA CLEMATITIS ROOT; ARTEMISIA ABROTANUM FLOWERING TOP; CROTALUS HORRIDUS HORRIDUS VENOM; ECHINACEA ANGUSTIFOLIA; KEROSENE; LACHESIS MUTA VENOM; MERCURIUS SOLUBILIS; SCROPHULARIA NODOSA; THUJA OCCIDENTALIS LEAFY TWIGAn 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; 6; 3; 10; 1; 3; 8; 12; 1; 10 
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 

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: 3/6/2026

Previous Code
Next Code