Search Icon


Drug Information

Product NDC: 43853-0042

Proprietary Name: Lung Detox

Non Proprietary Name: Argentum nitricum, Arsenicum album, Carduus marianus, Hepar suis, Mercurius corrosivus, Plumbum metallicum

Active Ingredient(s):
  • 200 [hp_C]/30mL ARSENIC TRIOXIDE;
  • 200 [hp_C]/30mL LEAD;
  • 200 [hp_C]/30mL MERCURIC CHLORIDE;
  • 1 [hp_X]/30mL MILK THISTLE;
  • 6 [hp_X]/30mL PORK LIVER;
  • 200 [hp_C]/30mL SILVER NITRATE

Administration Route(s): ORAL

Dosage Form(s): LIQUID

Labeler Information

Labeler Name: ProBLEN
Product Type: HUMAN OTC DRUG
FDA Application Number:
Start Marketing Date:4/15/2021

Package Information

No. Package Code Package Description Billing Unit
143853-0042-130 mL in 1 BOTTLE (43853-0042-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43853-0042The 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 NAMELung DetoxThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEArgentum nitricum, Arsenicum album, Carduus marianus, Hepar suis, Mercurius corrosivus, Plumbum metallicumThe 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 DATE4/15/2021This 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 under Structured Product Labeling Resources.
LABELER NAMEProBLENName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEARSENIC TRIOXIDE; LEAD; MERCURIC CHLORIDE; MILK THISTLE; PORK LIVER; SILVER NITRATEAn 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 STRENGTH200; 200; 200; 1; 6; 200 
ACTIVE INGRED UNIT[hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_C]/30mL 

Download Record

Download this NDC record in Text format: Export

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

Download this NDC record in XML format: Export

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