63083-6023 NDC - FOOD POISONING DETOX

Drug Information

Product NDC: 63083-6023

Proprietary Name: Food Poisoning Detox

Non Proprietary Name: Food Poisoning Detox

Active Ingredient(s):
  • 6 [hp_X]/59mL ACONITUM LYCOCTONUM WHOLE;
  • 3 [hp_X]/59mL ACONITUM NAPELLUS WHOLE;
  • 6 [hp_X]/59mL ARSENIC TRIOXIDE;
  • 6 [hp_X]/59mL CITRULLUS COLOCYNTHIS FRUIT PULP;
  • 30 [hp_X]/59mL CLOSTRIDIUM BOTULINUM;
  • 30 [hp_X]/59mL CLOSTRIDIUM DIFFICILE;
  • 1 [hp_X]/59mL ECHINACEA PURPUREA WHOLE;
  • 30 [hp_X]/59mL ESCHERICHIA COLI;
  • 30 [hp_X]/59mL GIBBERELLA FUJIKUROI;
  • 1 [hp_X]/59mL GLYCYRRHIZA GLABRA;
  • 5 [hp_X]/59mL GOLDENSEAL;
  • 30 [hp_X]/59mL HELICOBACTER PYLORI;
  • 30 [hp_X]/59mL KLEBSIELLA PNEUMONIAE;
  • 30 [hp_X]/59mL LISTERIA MONOCYTOGENES;
  • 30 [hp_X]/59mL MERCURIC CHLORIDE;
  • 30 [hp_X]/59mL MERCURIUS SOLUBILIS;
  • 6 [hp_X]/59mL PODOPHYLLUM;
  • 30 [hp_X]/59mL SALMONELLA ENTERICA ENTERICA SEROVAR TYPHI;
  • 30 [hp_X]/59mL STAPHYLOCOCCUS AUREUS;
  • 30 [hp_X]/59mL STREPTOCOCCUS PYOGENES;
  • 30 [hp_X]/59mL YERSINIA ENTEROCOLITICA


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Allergens [CS];
  • Allergens [CS];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Dietary Proteins [CS];
  • Fungal Proteins [CS];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased IgG Production [PE];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Non-Standardized Fungal Allergenic Extract [EPC];
  • Non-Standardized Plant Allergenic Extract [EPC];
  • Plant Proteins [CS]

Labeler Information

Labeler Name: Professional Complementary Health Formulas
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:8/15/1984

Package Information

No. Package Code Package Description Billing Unit
163083-6023-259 mL in 1 BOTTLE, DROPPER (63083-6023-2)

NDC Record

Field Name Field Value Definition
PRODUCT NDC63083-6023The 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 NAMEFood Poisoning DetoxThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIX6023A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
NON PROPRIETARY NAMEFood Poisoning DetoxThe 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 DATE8/15/1984This 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 NAMEProfessional Complementary Health FormulasName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACONITUM LYCOCTONUM WHOLE; ACONITUM NAPELLUS WHOLE; ARSENIC TRIOXIDE; CITRULLUS COLOCYNTHIS FRUIT PULP; CLOSTRIDIUM BOTULINUM; CLOSTRIDIUM DIFFICILE; ECHINACEA PURPUREA WHOLE; ESCHERICHIA COLI; GIBBERELLA FUJIKUROI; GLYCYRRHIZA GLABRA; GOLDENSEAL; HELICOBACTER PYLORI; KLEBSIELLA PNEUMONIAE; LISTERIA MONOCYTOGENES; MERCURIC CHLORIDE; MERCURIUS SOLUBILIS; PODOPHYLLUM; SALMONELLA ENTERICA ENTERICA SEROVAR TYPHI; STAPHYLOCOCCUS AUREUS; STREPTOCOCCUS PYOGENES; YERSINIA ENTEROCOLITICAAn 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 STRENGTH6; 3; 6; 6; 30; 30; 1; 30; 30; 1; 5; 30; 30; 30; 30; 30; 6; 30; 30; 30; 30 
ACTIVE INGRED UNIT[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL 
PHARM CLASSESAllergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Fungal Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS] 

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