43853-0041 NDC - METALS DETOX (ALUMINA, ARSENICUM METALLICUM, MERCURIUS CORROSIVUS, NICCOLUM METALLICUM, PLUMBUM METALLICUM, RADIUM BROMATUM, STANNUM METALLICUM)

Drug Information

Product NDC: 43853-0041

Proprietary Name: Metals Detox

Non Proprietary Name: Alumina, Arsenicum metallicum, Mercurius corrosivus, Niccolum metallicum, Plumbum metallicum, Radium bromatum, Stannum metallicum

Active Ingredient(s):
  • 30 [hp_C]/30mL ALUMINUM OXIDE;
  • 30 [hp_C]/30mL LEAD;
  • 30 [hp_C]/30mL MERCURIC CHLORIDE;
  • 30 [hp_C]/30mL NICKEL;
  • 30 [hp_C]/30mL RADIUM BROMIDE;
  • 30 [hp_C]/30mL TIN


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Allergens [CS];
  • Cell-mediated Immunity [PE];
  • Increased Histamine Release [PE];
  • Standardized Chemical Allergen [EPC]

Labeler Information

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

Package Information

No. Package Code Package Description Billing Unit
143853-0041-130 mL in 1 BOTTLE (43853-0041-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43853-0041The 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 NAMEMetals 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 NAMEAlumina, Arsenicum metallicum, Mercurius corrosivus, Niccolum metallicum, Plumbum metallicum, Radium bromatum, Stannum 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 www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMEProBLENName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEALUMINUM OXIDE; LEAD; MERCURIC CHLORIDE; NICKEL; RADIUM BROMIDE; TINAn 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 
ACTIVE INGRED UNIT[hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL 
PHARM CLASSESAllergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC] 

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