43406-0019 NDC - ECZEMA HP (ARSENIC TRIOXIDE 30X, OYSTER SHELL CALCIUM CARBONATE, CRUDE 30X, GRAPHITE 30X, MERCURIUS SOLUBILIS 30X, DAPHNE MEZEREUM BARK 30X, TOXICODENDRON PUBESCENS LEAF 30X, SEPIA OFFICINALIS JUICE 30X, SULFUR 30X)

Drug Information

Product NDC: 43406-0019

Proprietary Name: ECZEMA HP

Non Proprietary Name: Arsenic Trioxide 30X, Oyster Shell Calcium Carbonate, Crude 30X, Graphite 30X, Mercurius Solubilis 30X, Daphne Mezereum Bark 30X, Toxicodendron Pubescens Leaf 30X, Sepia Officinalis Juice 30X, Sulfur 30X

Active Ingredient(s):
  • 30 [hp_X]/mL ARSENIC TRIOXIDE;
  • 30 [hp_X]/mL DAPHNE MEZEREUM BARK;
  • 30 [hp_X]/mL GRAPHITE;
  • 30 [hp_X]/mL MERCURIUS SOLUBILIS;
  • 30 [hp_X]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE;
  • 30 [hp_X]/mL SEPIA OFFICINALIS JUICE;
  • 30 [hp_X]/mL SULFUR;
  • 30 [hp_X]/mL TOXICODENDRON PUBESCENS LEAF


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Labeler Information

Labeler Name: Natural Creations, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:5/29/2007

Package Information

No. Package Code Package Description Billing Unit
143406-0019-130 mL in 1 BOTTLE, DROPPER (43406-0019-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43406-0019The 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 NAMEECZEMA HPThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEArsenic Trioxide 30X, Oyster Shell Calcium Carbonate, Crude 30X, Graphite 30X, Mercurius Solubilis 30X, Daphne Mezereum Bark 30X, Toxicodendron Pubescens Leaf 30X, Sepia Officinalis Juice 30X, Sulfur 30XThe 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.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE5/29/2007This 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 NAMENatural Creations, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEARSENIC TRIOXIDE; DAPHNE MEZEREUM BARK; GRAPHITE; MERCURIUS SOLUBILIS; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SEPIA OFFICINALIS JUICE; SULFUR; 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 STRENGTH30; 30; 30; 30; 30; 30; 30; 30 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 

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