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,

Biotics Research Corporation
Human Otc Drug
NDC 55146-011

1 Detoxification also known as 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, is a human otc drug labeled by 'Biotics Research Corporation'. National Drug Code (NDC) number for 1 Detoxification is 55146-011. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in 1 Detoxification drug includes Activated Charcoal - 30 [hp_C]/mL Alcohol, X-ray Exposed (1000 Rad) - 30 [hp_C]/mL Allylthiourea - 30 [hp_C]/mL Aluminum - 12 [hp_X]/mL Anguilla Rostrata Blood Serum - 30 [hp_X]/mL Antimony Trisulfide - 12 [hp_X]/mL Apis Mellifera - 30 [hp_C]/mL Arsenic Trioxide - 12 [hp_X]/mL Bacillus Anthracis Immunoserum Rabbit - 30 [hp_X]/mL Barium Carbonate - 12 [hp_X]/mL and more. The currest status of 1 Detoxification drug is Active.

Drug Information:

Drug NDC:	55146-011
The 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.
Proprietary Name:	1 Detoxification
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type:	Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
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,
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Biotics Research Corporation
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Liquid
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status:	Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:	ACTIVATED CHARCOAL - 30 [hp_C]/mL ALCOHOL, X-RAY EXPOSED (1000 RAD) - 30 [hp_C]/mL ALLYLTHIOUREA - 30 [hp_C]/mL ALUMINUM - 12 [hp_X]/mL ANGUILLA ROSTRATA BLOOD SERUM - 30 [hp_X]/mL ANTIMONY TRISULFIDE - 12 [hp_X]/mL APIS MELLIFERA - 30 [hp_C]/mL ARSENIC TRIOXIDE - 12 [hp_X]/mL BACILLUS ANTHRACIS IMMUNOSERUM RABBIT - 30 [hp_X]/mL BARIUM CARBONATE - 12 [hp_X]/mL Load more... BERYLLIUM - 12 [hp_X]/mL BISMUTH - 12 [hp_X]/mL BORON - 12 [hp_X]/mL BROMINE - 12 [hp_X]/mL CADMIUM - 12 [hp_X]/mL CAPSICUM - 3 [hp_X]/mL CARBO ANIMALIS - 30 [hp_C]/mL CERIUM - 12 [hp_X]/mL CESIUM CHLORIDE - 12 [hp_X]/mL CHROMIUM - 12 [hp_X]/mL CLAVICEPS PURPUREA SCLEROTIUM - 30 [hp_C]/mL COBALT - 12 [hp_X]/mL CONIUM MACULATUM FLOWERING TOP - 30 [hp_C]/mL COPPER - 12 [hp_X]/mL CORTICOTROPIN - 30 [hp_C]/mL DYSPROSIUM - 12 [hp_X]/mL ERBIUM - 12 [hp_X]/mL EUROPIUM - 12 [hp_X]/mL GADOLINIUM - 12 [hp_X]/mL GELSEMIUM SEMPERVIRENS ROOT - 30 [hp_C]/mL GERMANIUM SESQUIOXIDE - 12 [hp_X]/mL GOLD - 12 [hp_X]/mL HOLMIUM - 12 [hp_X]/mL HUMAN BREAST TUMOR CELL - 30 [hp_C]/mL INDIUM - 12 [hp_X]/mL IRON - 12 [hp_X]/mL LACHESIS MUTA VENOM - 30 [hp_C]/mL LANTHANUM - 14 [hp_C]/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 - 12 [hp_X]/mL NIOBIUM - 30 [hp_C]/mL OSMIUM - 12 [hp_X]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE - 30 [hp_C]/mL PALLADIUM - 12 [hp_X]/mL PHOSPHORIC ACID - 30 [hp_C]/mL PHOSPHORUS - 30 [hp_C]/mL PHYTOLACCA AMERICANA ROOT - 4 [hp_X]/mL PLATINUM - 12 [hp_X]/mL POTASSIUM DICHROMATE - 30 [hp_C]/mL PRASEODYMIUM - 12 [hp_X]/mL RANCID BEEF - 30 [hp_C]/mL RHODIUM - 12 [hp_X]/mL RUBIDIUM NITRITE - 12 [hp_X]/mL SAMARIUM - 12 [hp_X]/mL SELENIUM - 12 [hp_X]/mL SILVER - 12 [hp_X]/mL SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE - 30 [hp_C]/mL STRONTIUM CARBONATE - 12 [hp_X]/mL STRYCHNOS WALLICHIANA BARK - 30 [hp_C]/mL SULFURIC ACID - 30 [hp_C]/mL SUS SCROFA PITUITARY GLAND - 30 [hp_X]/mL SUS SCROFA THYROID - 30 [hp_X]/mL TANTALUM - 30 [hp_C]/mL TARTARIC ACID - 30 [hp_X]/mL TERBIUM - 12 [hp_X]/mL THALLIUM - 12 [hp_X]/mL THERIDION CURASSAVICUM - 30 [hp_X]/mL THUJA OCCIDENTALIS LEAFY TWIG - 30 [hp_C]/mL TIN - 12 [hp_X]/mL TRIFOLIUM PRATENSE FLOWER - 3 [hp_X]/mL URANYL NITRATE HEXAHYDRATE - 12 [hp_X]/mL VANADIUM - 12 [hp_X]/mL VERATRUM ALBUM ROOT - 30 [hp_C]/mL YTTERBIUM OXIDE - 12 [hp_X]/mL ZINC - 12 [hp_X]/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Marketing Category:	UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date:	05 May, 2020
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	16 Jun, 2026
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Listing Expiration Date:	31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Manufacturer Name:	Biotics Research Corporation
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:	Yes
Whether or not the drug has been repackaged for distribution.
NUI:	N0000185021 N0000175629 N0000184306 N0000185001 M0000728 M0002274 N0000185375 N0000185371 M0006342 M0016962 M0022575 N0000185508 M0005152 N0000175831 N0000008595 N0000008924 N0000175830 M0000499 N0000175941
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	2P3VWU3H10 6PRJ93602P 706IDJ14B7 CPD4NFA903 L7B16ESD1U F79059A38U 7S82P3R43Z S7V92P67HO 41LZ22DD4N 6P669D8HQ8 Load more... OW5102UV6N U015TT5I8H N9E3X5056Q SBV4XY874G 00BH33GNGH 00UK7646FG 279O8I0433 30K4522N6T GNR9HML8BA 0R0008Q3JB 01G9XEA93N 3G0H8C9362 Q28R5GF371 789U1901C5 K0U68Q2TXA 1D4N45714Q 77B218D3YE 444W947O8O AU0V1LM3JT 639KR60Q1Q 96WE91N25T 79Y1949PYO W1XX32SQN1 C62OO7VD9K 045A6V3VFX E1UOL152H7 VSW71SS07I 6I3K30563S 2P299V784P 2BMD2GNA4V I38ZP9992A 42Z2K6ZL8P 324Y4038G2 81AH48963U AYT3H319PN 7OV03QG267 05175J654G 2E7M255OPY 2E32821G6I 5TWQ1V240M E4GA8884NN 27YLU75U4W 11E6VI8VEG 49DFR088MY T4423S18FM NKN7EZA750 29SUH5R3HU DMK383DSAC 93722E7JA1 42OD65L39F H6241UJ22B 3M4G523W1G 70WT22SF4B 41YPU4MMCA OQ16ZEE7O7 O40UQP6WCF L0PFEMQ1DT 6RV024OAUQ 6424HBN274 W4888I119H 06SSF7P179 AD84R52XLF 9Z8D3HEM8L 1NT28V9397 387GMG9FH5 4JS0838828 3V057702FY 00J9J9XKDE QNS6W5US1Z T66CZ53RP4 J41CSQ7QDS
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class EPC:	Standardized Insect Venom Allergenic Extract [EPC] Non-Standardized Plant Allergenic Extract [EPC] Non-Standardized Food Allergenic Extract [EPC] Standardized Chemical Allergen [EPC] Copper-containing Intrauterine Device [EPC] Adrenocorticotropic Hormone [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class PE:	Increased Histamine Release [PE] Cell-mediated Immunity [PE] Increased IgG Production [PE] Decreased Embryonic Implantation [PE] Decreased Sperm Motility [PE] Inhibit Ovum Fertilization [PE]
Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`.
Pharmacologic Class CS:	Allergens [CS] Bee Venoms [CS] Dietary Proteins [CS] Plant Proteins [CS] Vegetable Proteins [CS] Copper [CS] Adrenocorticotropic Hormone [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:	Adrenocorticotropic Hormone [CS] Adrenocorticotropic Hormone [EPC] Allergens [CS] Bee Venoms [CS] 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 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 Insect Venom Allergenic Extract [EPC] Vegetable Proteins [CS]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
55146-011-01	120 mL in 1 BOTTLE (55146-011-01)	05 May, 2020	N/A	No
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Other medicines with the same generic name

1 Detoxification

Trifolium Pratense & more..

Liquid
Biotics Research Corporation
NDC: 55146-011

Purpose:

Indications: for temporary relief of gastrointestinal dyspepsia (indigestion) with flatulence, bloating and intolerance of certain foods. remedy #1 supports detoxification and cellular repair.

Product Elements:

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, trifolium pratense flower trifolium pratense flower capsicum capsicum phytolacca americana root phytolacca americana root aluminum aluminum antimony trisulfide antimony trisulfide silver silver arsenic trioxide arsenic cation (3+) gold gold barium carbonate barium cation beryllium beryllium bismuth bismuth boron boron bromine bromine cadmium cadmium cerium cerium cesium chloride cesium cation chromium chromium cobalt cobalt copper copper dysprosium dysprosium erbium erbium europium europium iron iron gadolinium gadolinium germanium sesquioxide germanium sesquioxide holmium holmium indium indium lithium carbonate lithium cation magnesium magnesium manganese manganese mercurius solubilis mercurius solubilis molybdenum molybdenum neodymium oxide neodymium oxide nickel nickel osmium osmium palladium palladium platinum platinum lead lead praseodymium praseodymium rhodium rhodium rubidium nitrite rubidium cation nitrite ion samarium samarium selenium selenium tin tin strontium carbonate strontium cation terbium terbium thallium thallium uranyl nitrate hexahydrate uranium cation (6+) vanadium vanadium ytterbium oxide ytterbium oxide zinc zinc bacillus anthracis immunoserum rabbit bacillus anthracis immunoserum rabbit sus scrofa pituitary gland sus scrofa pituitary gland anguilla rostrata blood serum anguilla rostrata blood serum tartaric acid tartaric acid theridion curassavicum theridion curassavicum sus scrofa thyroid sus scrofa thyroid lanthanum lanthanum corticotropin corticotropin apis mellifera apis mellifera oyster shell calcium carbonate, crude oyster shell calcium carbonate, crude carbo animalis carbo animalis activated charcoal activated charcoal human breast tumor cell human breast tumor cell conium maculatum flowering top conium maculatum flowering top gelsemium sempervirens root gelsemium sempervirens root strychnos wallichiana bark strychnos wallichiana bark potassium dichromate dichromate ion lachesis muta venom lachesis muta venom sodium phosphate, dibasic, heptahydrate phosphate ion niobium niobium phosphoric acid phosphoric acid phosphorus phosphorus rancid beef rancid beef claviceps purpurea sclerotium claviceps purpurea sclerotium sulfuric acid sulfuric acid tantalum tantalum allylthiourea allylthiourea thuja occidentalis leafy twig thuja occidentalis leafy twig veratrum album root veratrum album root alcohol, x-ray exposed (1000 rad) alcohol, x-ray exposed (1000 rad) citric acid monohydrate sodium benzoate alcohol water

Indications and Usage:

Indications: for temporary relief of gastrointestinal dyspepsia (indigestion) with flatulence, bloating and intolerance of certain foods. remedy #1 supports detoxification and cellular repair.

Warnings:

Warnings: if symptoms persist or worsen, seek the advice of a healthcare professional. caution: not recommended for pregnant or lactating women. keep out of reach of children in case of overdose, get medical help or contact a poison control center right away. tamper seal: sealed with an imprinted safety seal for your protection. do not use if seal is missing or broken.

Dosage and Administration:

Directions: one (1) teaspoon twice daily or as otherwise directed by a healthcare professional. consult a physician for use in children under 6 years of age.

Package Label Principal Display Panel:

Package label display: biotics research corporation's 21st century homeopathics ndc #55146-011-01 homeopathic remedy #1 detoxification water based formula 4 fl. oz. (120 ml) 1 detoxification

Further Questions:

Questions: distributed by biotics research corporation rosenberg, tx 77471 â¢ (281) 344-0909

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.