55146-011 NDC - 1 DETOXIFICATION (TRIFOLIUM PRATENSE, CAPSICUM ANNUUM, PHYTOLACCA DECANDRA, ALUMINUM METALLICUM, ANTIMONIUM CRUDUM, ARGENTUM METALLICUM, ARSENICUM ALBUM, AURUM METALLICUM, BARYTA CARBONICA, BERYLLIUM METALLICUM, BISMUTHUM METALLICUM, BORON, BROMIUM, CADMIUM METALLICUM, CERIUM METALLICUM, CESIUM CHLORIDE, CHROMIUM, COBALTUM METALLICUM, CUPRUM METALLICUM, DYSPROSIUM METALLICUM, ERBIUM METALLICUM, EUROPIUM OXYDATUM, FERRUM METALLICUM, GADOLINIUM METALLICUM, GERMANIUM SESQUIOXIDE, HOLMIUM METALLICUM, INDIUM METALLICUM,)

Drug Information

Product NDC: 55146-011

Proprietary Name: 1 Detoxification

Non Proprietary Name: Trifolium Pratense, Capsicum Annuum, Phytolacca Decandra, Aluminum Metallicum, Antimonium Crudum, Argentum Metallicum, Arsenicum Album, Aurum Metallicum, Baryta Carbonica, Beryllium Metallicum, Bismuthum Metallicum, Boron, Bromium, Cadmium Metallicum, Cerium Metallicum, Cesium Chloride, Chromium, Cobaltum Metallicum, Cuprum Metallicum, Dysprosium Metallicum, Erbium Metallicum, Europium Oxydatum, Ferrum Metallicum, Gadolinium Metallicum, Germanium Sesquioxide, Holmium Metallicum, Indium Metallicum,

Active Ingredient(s):
  • 30 [hp_C]/mL ACTIVATED CHARCOAL;
  • 30 [hp_C]/mL ALCOHOL, X-RAY EXPOSED (1000 RAD);
  • 30 [hp_C]/mL ALLYLTHIOUREA;
  • 12 [hp_X]/mL ALUMINUM;
  • 30 [hp_X]/mL ANGUILLA ROSTRATA BLOOD SERUM;
  • 12 [hp_X]/mL ANTIMONY TRISULFIDE;
  • 30 [hp_C]/mL APIS MELLIFERA;
  • 12 [hp_X]/mL ARSENIC TRIOXIDE;
  • 30 [hp_X]/mL BACILLUS ANTHRACIS IMMUNOSERUM RABBIT;
  • 12 [hp_X]/mL BARIUM CARBONATE;
  • 12 [hp_X]/mL BERYLLIUM;
  • 12 [hp_X]/mL BISMUTH;
  • 12 [hp_X]/mL BORON;
  • 12 [hp_X]/mL BROMINE;
  • 12 [hp_X]/mL CADMIUM;
  • 3 [hp_X]/mL CAPSICUM;
  • 30 [hp_C]/mL CARBO ANIMALIS;
  • 12 [hp_X]/mL CERIUM;
  • 12 [hp_X]/mL CESIUM CHLORIDE;
  • 12 [hp_X]/mL CHROMIUM;
  • 30 [hp_C]/mL CLAVICEPS PURPUREA SCLEROTIUM;
  • 12 [hp_X]/mL COBALT;
  • 30 [hp_C]/mL CONIUM MACULATUM FLOWERING TOP;
  • 12 [hp_X]/mL COPPER;
  • 30 [hp_C]/mL CORTICOTROPIN;
  • 12 [hp_X]/mL DYSPROSIUM;
  • 12 [hp_X]/mL ERBIUM;
  • 12 [hp_X]/mL EUROPIUM;
  • 12 [hp_X]/mL GADOLINIUM;
  • 30 [hp_C]/mL GELSEMIUM SEMPERVIRENS ROOT;
  • 12 [hp_X]/mL GERMANIUM SESQUIOXIDE;
  • 12 [hp_X]/mL GOLD;
  • 12 [hp_X]/mL HOLMIUM;
  • 30 [hp_C]/mL HUMAN BREAST TUMOR CELL;
  • 12 [hp_X]/mL INDIUM;
  • 12 [hp_X]/mL IRON;
  • 30 [hp_C]/mL LACHESIS MUTA VENOM;
  • 14 [hp_C]/mL LANTHANUM;
  • 12 [hp_X]/mL LEAD;
  • 12 [hp_X]/mL LITHIUM CARBONATE;
  • 12 [hp_X]/mL MAGNESIUM;
  • 12 [hp_X]/mL MANGANESE;
  • 12 [hp_X]/mL MERCURIUS SOLUBILIS;
  • 12 [hp_X]/mL MOLYBDENUM;
  • 12 [hp_X]/mL NEODYMIUM OXIDE;
  • 12 [hp_X]/mL NICKEL;
  • 30 [hp_C]/mL NIOBIUM;
  • 12 [hp_X]/mL OSMIUM;
  • 30 [hp_C]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE;
  • 12 [hp_X]/mL PALLADIUM;
  • 30 [hp_C]/mL PHOSPHORIC ACID;
  • 30 [hp_C]/mL PHOSPHORUS;
  • 4 [hp_X]/mL PHYTOLACCA AMERICANA ROOT;
  • 12 [hp_X]/mL PLATINUM;
  • 30 [hp_C]/mL POTASSIUM DICHROMATE;
  • 12 [hp_X]/mL PRASEODYMIUM;
  • 30 [hp_C]/mL RANCID BEEF;
  • 12 [hp_X]/mL RHODIUM;
  • 12 [hp_X]/mL RUBIDIUM NITRITE;
  • 12 [hp_X]/mL SAMARIUM;
  • 12 [hp_X]/mL SELENIUM;
  • 12 [hp_X]/mL SILVER;
  • 30 [hp_C]/mL SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE;
  • 12 [hp_X]/mL STRONTIUM CARBONATE;
  • 30 [hp_C]/mL STRYCHNOS WALLICHIANA BARK;
  • 30 [hp_C]/mL SULFURIC ACID;
  • 30 [hp_X]/mL SUS SCROFA PITUITARY GLAND;
  • 30 [hp_X]/mL SUS SCROFA THYROID;
  • 30 [hp_C]/mL TANTALUM;
  • 30 [hp_X]/mL TARTARIC ACID;
  • 12 [hp_X]/mL TERBIUM;
  • 12 [hp_X]/mL THALLIUM;
  • 30 [hp_X]/mL THERIDION CURASSAVICUM;
  • 30 [hp_C]/mL THUJA OCCIDENTALIS LEAFY TWIG;
  • 12 [hp_X]/mL TIN;
  • 3 [hp_X]/mL TRIFOLIUM PRATENSE FLOWER;
  • 12 [hp_X]/mL URANYL NITRATE HEXAHYDRATE;
  • 12 [hp_X]/mL VANADIUM;
  • 30 [hp_C]/mL VERATRUM ALBUM ROOT;
  • 12 [hp_X]/mL YTTERBIUM OXIDE;
  • 12 [hp_X]/mL ZINC


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Adrenocorticotropic Hormone [CS];
  • Adrenocorticotropic Hormone [EPC];
  • Allergens [CS];
  • Allergens [CS];
  • Allergens [CS];
  • Allergens [CS];
  • Allergens [CS];
  • Allergens [CS];
  • Bee Venoms [CS];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Copper [CS];
  • Copper-containing Intrauterine Device [EPC];
  • Decreased Embryonic Implantation [PE];
  • Decreased Sperm Motility [PE];
  • Dietary Proteins [CS];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased IgG Production [PE];
  • Inhibit Ovum Fertilization [PE];
  • Mood Stabilizer [EPC];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Non-Standardized Plant Allergenic Extract [EPC];
  • Plant Proteins [CS];
  • Standardized Chemical Allergen [EPC];
  • Standardized Chemical Allergen [EPC];
  • Standardized Chemical Allergen [EPC];
  • Standardized Chemical Allergen [EPC];
  • Standardized Insect Venom Allergenic Extract [EPC];
  • Vegetable Proteins [CS]

Labeler Information

Labeler Name: Biotics Research Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:5/5/2020

Package Information

No. Package Code Package Description Billing Unit
155146-011-01120 mL in 1 BOTTLE (55146-011-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC55146-011The 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 NAME1 DetoxificationThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMETrifolium Pratense, Capsicum Annuum, Phytolacca Decandra, Aluminum Metallicum, Antimonium Crudum, Argentum Metallicum, Arsenicum Album, Aurum Metallicum, Baryta Carbonica, Beryllium Metallicum, Bismuthum Metallicum, Boron, Bromium, Cadmium Metallicum, Cerium Metallicum, Cesium Chloride, Chromium, Cobaltum Metallicum, Cuprum Metallicum, Dysprosium Metallicum, Erbium Metallicum, Europium Oxydatum, Ferrum Metallicum, Gadolinium Metallicum, Germanium Sesquioxide, Holmium Metallicum, Indium Metallicum,The 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 DATE5/5/2020This 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 NAMEBiotics Research CorporationName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACTIVATED CHARCOAL; ALCOHOL, X-RAY EXPOSED (1000 RAD); ALLYLTHIOUREA; ALUMINUM; ANGUILLA ROSTRATA BLOOD SERUM; ANTIMONY TRISULFIDE; APIS MELLIFERA; ARSENIC TRIOXIDE; BACILLUS ANTHRACIS IMMUNOSERUM RABBIT; BARIUM CARBONATE; BERYLLIUM; BISMUTH; BORON; BROMINE; CADMIUM; CAPSICUM; CARBO ANIMALIS; CERIUM; CESIUM CHLORIDE; CHROMIUM; CLAVICEPS PURPUREA SCLEROTIUM; COBALT; CONIUM MACULATUM FLOWERING TOP; COPPER; CORTICOTROPIN; DYSPROSIUM; ERBIUM; EUROPIUM; GADOLINIUM; GELSEMIUM SEMPERVIRENS ROOT; GERMANIUM SESQUIOXIDE; GOLD; HOLMIUM; HUMAN BREAST TUMOR CELL; INDIUM; IRON; LACHESIS MUTA VENOM; LANTHANUM; LEAD; LITHIUM CARBONATE; MAGNESIUM; MANGANESE; MERCURIUS SOLUBILIS; MOLYBDENUM; NEODYMIUM OXIDE; NICKEL; NIOBIUM; OSMIUM; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PALLADIUM; PHOSPHORIC ACID; PHOSPHORUS; PHYTOLACCA AMERICANA ROOT; PLATINUM; POTASSIUM DICHROMATE; PRASEODYMIUM; RANCID BEEF; RHODIUM; RUBIDIUM NITRITE; SAMARIUM; SELENIUM; SILVER; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; STRONTIUM CARBONATE; STRYCHNOS WALLICHIANA BARK; SULFURIC ACID; SUS SCROFA PITUITARY GLAND; SUS SCROFA THYROID; TANTALUM; TARTARIC ACID; TERBIUM; THALLIUM; THERIDION CURASSAVICUM; THUJA OCCIDENTALIS LEAFY TWIG; TIN; TRIFOLIUM PRATENSE FLOWER; URANYL NITRATE HEXAHYDRATE; VANADIUM; VERATRUM ALBUM ROOT; YTTERBIUM OXIDE; ZINCAn 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; 12; 30; 12; 30; 12; 30; 12; 12; 12; 12; 12; 12; 3; 30; 12; 12; 12; 30; 12; 30; 12; 30; 12; 12; 12; 12; 30; 12; 12; 12; 30; 12; 12; 30; 14; 12; 12; 12; 12; 12; 12; 12; 12; 30; 12; 30; 12; 30; 30; 4; 12; 30; 12; 30; 12; 12; 12; 12; 12; 30; 12; 30; 30; 30; 30; 30; 30; 12; 12; 30; 30; 12; 3; 12; 12; 30; 12; 12 
ACTIVE INGRED UNIT[hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESAdrenocorticotropic Hormone [CS], Adrenocorticotropic Hormone [EPC], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Inhibit Ovum Fertilization [PE], Mood Stabilizer [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC], Standardized Insect Venom Allergenic Extract [EPC], Vegetable Proteins [CS] 

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