59469-203 NDC - VULPUR (SILVER NITRATE, ARMORACIA RUSTICANA WHOLE, CINNAMOMUM VERUM WHOLE, WOOD CREOSOTE, CAPSELLA BURSA-PASTORIS, CALENDULA OFFICINALIS FLOWERING TOP, ACHILLEA MILLEFOLIUM, AND SALVIA OFFICINALIS FLOWERING TOP)

Drug Information

Product NDC: 59469-203

Proprietary Name: VULPUR

Non Proprietary Name: Silver Nitrate, Armoracia rusticana whole, Cinnamomum verum whole, Wood Creosote, Capsella bursa-pastoris, Calendula Officinalis Flowering Top, Achillea Millefolium, and Salvia officinalis flowering top

Active Ingredient(s):
  • 8 [hp_X]/50mL ACHILLEA MILLEFOLIUM WHOLE;
  • 4 [hp_X]/50mL ARMORACIA RUSTICANA WHOLE;
  • 8 [hp_X]/50mL CALENDULA OFFICINALIS FLOWERING TOP;
  • 4 [hp_X]/50mL CAPSELLA BURSA-PASTORIS WHOLE;
  • 12 [hp_X]/50mL CINNAMOMUM VERUM WHOLE;
  • 8 [hp_X]/50mL SALVIA OFFICINALIS FLOWERING TOP;
  • 6 [hp_X]/50mL SILVER NITRATE;
  • 6 [hp_X]/50mL WOOD CREOSOTE


Administration Route(s): ORAL

Dosage Form(s): SOLUTION/ DROPS

Labeler Information

Labeler Name: PEKANA Naturheilmittel GmbH
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:10/1/2017

Package Information

No. Package Code Package Description Billing Unit
159469-203-101 BOTTLE, GLASS in 1 BOX (59469-203-10) / 50 mL in 1 BOTTLE, GLASS

NDC Record

Field Name Field Value Definition
PRODUCT NDC59469-203The 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 NAMEVULPURThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMESilver Nitrate, Armoracia rusticana whole, Cinnamomum verum whole, Wood Creosote, Capsella bursa-pastoris, Calendula Officinalis Flowering Top, Achillea Millefolium, and Salvia officinalis flowering topThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESOLUTION/ DROPSThe 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 DATE10/1/2017This 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 NAMEPEKANA Naturheilmittel GmbHName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACHILLEA MILLEFOLIUM WHOLE; ARMORACIA RUSTICANA WHOLE; CALENDULA OFFICINALIS FLOWERING TOP; CAPSELLA BURSA-PASTORIS WHOLE; CINNAMOMUM VERUM WHOLE; SALVIA OFFICINALIS FLOWERING TOP; SILVER NITRATE; WOOD CREOSOTEAn 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 STRENGTH8; 4; 8; 4; 12; 8; 6; 6 
ACTIVE INGRED UNIT[hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL 

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This page was last updated on: 2/1/2023