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NDC 50181-0075 Biotox Bac I

Cochlearia Armoracia,Taraxacum Officinale,Tabebuia Impetiginosa,Brucella - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 50181-0075?
  4. Biotox Bac I Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Get all the details for National Drug Code (NDC) 50181-0075 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
50181-0075
Proprietary Name:
Biotox Bac I
Non-Proprietary Name: [1]
Cochlearia Armoracia, Taraxacum Officinale, Tabebuia Impetiginosa, Brucella Abortus, Colibacillinum Cum Natrum Muriaticum, Germanium, Pertussinum, Anthracinum, Bacillus Tetani, Pyrogenium, Francisella Tularensis, Yersinia Enterocolitica, Brucella Melitensis, Serratia Marcescens, Citrobacter Diversus, Enterobacter Aerogenes, Pestinum, Bacillus Cereus, Pseudomonas Aeruginosa, Coxiella Burnetii, Proteus (mirabilis)
Substance Name: [2]
Bacillus Anthracis Immunoserum Rabbit; Bacillus Cereus; Brucella Abortus; Brucella Melitensis; Citrobacter Koseri; Clostridium Tetani; Coxiella Burnetii; Enterobacter Aerogenes; Escherichia Coli; Francisella Tularensis; Germanium; Horseradish; Human Sputum, Bordetella Pertussis Infected; Proteus Mirabilis; Pseudomonas Aeruginosa; Rancid Beef; Serratia Marcescens; Tabebuia Impetiginosa Bark; Taraxacum Officinale; Yersinia Enterocolitica; Yersinia Pestis
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.
Labeler Name: [5]
The Wellness Center For Research
Labeler Code:
50181
Product Label ID:
df12608a-d29e-4c95-ac06-bbf2c38ba007
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
05-04-2021
End Marketing Date: [10]
08-23-2026
Exclude Flag: [12]
N
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Product Details

What is NDC 50181-0075?

The NDC code 50181-0075 is assigned by the FDA to the product Biotox Bac I which is a human over the counter drug product labeled by The Wellness Center For Research. The generic name of Biotox Bac I is cochlearia armoracia, taraxacum officinale, tabebuia impetiginosa, brucella abortus, colibacillinum cum natrum muriaticum, germanium, pertussinum, anthracinum, bacillus tetani, pyrogenium, francisella tularensis, yersinia enterocolitica, brucella melitensis, serratia marcescens, citrobacter diversus, enterobacter aerogenes, pestinum, bacillus cereus, pseudomonas aeruginosa, coxiella burnetii, proteus (mirabilis). The product's dosage form is liquid and is administered via oral form. The product is distributed in a single package with assigned NDC code 50181-0075-1 30 ml in 1 bottle, dropper . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Biotox Bac I?

Tired, rash, flu-like symptoms, swelling, joint pain, tingling, numbness in your hands, feet or back, brain fog, poor memory, weakness or paralysis in facial muscles. Tired, rash, flu-like symptoms, swelling, joint pain, tingling, numbness in your hands, feet or back, brain fog, poor memory, weakness or paralysis in facial muscles.

What are Biotox Bac I Active Ingredients?

An 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.
  • BACILLUS ANTHRACIS IMMUNOSERUM RABBIT 60 [hp_X]/mL
  • BACILLUS CEREUS 18 [hp_C]/mL - A species of rod-shaped bacteria that is a common soil saprophyte. Its spores are widespread and multiplication has been observed chiefly in foods. Contamination may lead to food poisoning.
  • BRUCELLA ABORTUS 12 [hp_X]/mL - A species of the genus BRUCELLA whose natural hosts are cattle and other bovidae. Abortion and placentitis are frequently produced in the pregnant animal. Other mammals, including humans, may be infected.
  • BRUCELLA MELITENSIS 9 [hp_C]/mL - A species of the genus BRUCELLA whose natural hosts are sheep and goats. Other mammals, including humans, may be infected. In general, these organisms tend to be more virulent for laboratory animals than BRUCELLA ABORTUS and may cause fatal infections.
  • CITROBACTER KOSERI 12 [hp_C]/mL - A species of gram-negative enterobacteria found in WATER; SEWAGE; SOIL; and FOOD. It can be present in any clinical specimen as an opportunistic pathogen.
  • CLOSTRIDIUM TETANI 60 [hp_X]/mL - The cause of TETANUS in humans and domestic animals. It is a common inhabitant of human and horse intestines as well as soil. Two components make up its potent exotoxin activity, a neurotoxin and a hemolytic toxin.
  • COXIELLA BURNETII 30 [hp_C]/mL - A species of gram-negative bacteria that grows preferentially in the vacuoles of the host cell. It is the etiological agent of Q FEVER.
  • ENTEROBACTER AEROGENES 15 [hp_C]/mL - Gram-negative, capsulated, gas-producing rods found widely in nature. Both motile and non-motile strains exist. The species is closely related to KLEBSIELLA PNEUMONIAE and is frequently associated with nosocomial infections
  • ESCHERICHIA COLI 12 [hp_X]/mL - A species of gram-negative, facultatively anaerobic, rod-shaped bacteria (GRAM-NEGATIVE FACULTATIVELY ANAEROBIC RODS) commonly found in the lower part of the intestine of warm-blooded animals. It is usually nonpathogenic, but some strains are known to produce DIARRHEA and pyogenic infections. Pathogenic strains (virotypes) are classified by their specific pathogenic mechanisms such as toxins (ENTEROTOXIGENIC ESCHERICHIA COLI), etc.
  • FRANCISELLA TULARENSIS 60 [hp_X]/mL - The etiologic agent of TULAREMIA in man and other warm-blooded animals.
  • GERMANIUM 15 [hp_X]/mL - A rare metal element with a blue-gray appearance and atomic symbol Ge, atomic number 32, and atomic weight 72.63.
  • HORSERADISH 3 [hp_X]/mL
  • HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED 30 [hp_X]/mL
  • PROTEUS MIRABILIS 30 [hp_C]/mL - A species of gram-negative, facultatively anaerobic, rod-shaped bacteria that is frequently isolated from clinical specimens. Its most common site of infection is the urinary tract.
  • PSEUDOMONAS AERUGINOSA 30 [hp_C]/mL - A species of gram-negative, aerobic, rod-shaped bacteria commonly isolated from clinical specimens (wound, burn, and urinary tract infections). It is also found widely distributed in soil and water. P. aeruginosa is a major agent of nosocomial infection.
  • RANCID BEEF 60 [hp_X]/mL
  • SERRATIA MARCESCENS 12 [hp_C]/mL - A species of gram-negative, facultatively anaerobic, rod-shaped bacteria found in soil, water, food, and clinical specimens. It is a prominent opportunistic pathogen for hospitalized patients.
  • TABEBUIA IMPETIGINOSA BARK 3 [hp_X]/mL
  • TARAXACUM OFFICINALE 3 [hp_X]/mL - A plant genus of the family Asteraceae. Members contain chicoric and chlorogenic acids and germacrane- and eudesmane-type SESQUITERPENES.
  • YERSINIA ENTEROCOLITICA 60 [hp_X]/mL - A species of the genus YERSINIA, isolated from both man and animal. It is a frequent cause of bacterial gastroenteritis in children.
  • YERSINIA PESTIS 15 [hp_C]/mL - The etiologic agent of PLAGUE in man, rats, ground squirrels, and other rodents.

Which are Biotox Bac I UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Biotox Bac I Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

Which are the Pharmacologic Classes for Biotox Bac I?

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Product Footnotes

[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

[2] What is the Substance Name? - An 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.

[3] What kind of product is this? - Indicates 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.

[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[8] What is the Marketing Category? - Product 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.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[10] What is the End Marketing Date? - 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.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".