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NDC 63083-9411 Intestinal Nosode Combination 9411

Liquid Oral - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 63083-9411?
  4. Intestinal Nosode Combination 9411 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) 63083-9411 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:
63083-9411
Proprietary Name:
Intestinal Nosode Combination 9411
Non-Proprietary Name: [1]
Intestinal Nosode Combination
Substance Name: [2]
Aloe; Cholera Enterotoxin Subunit B; Citrullus Colocynthis Fruit Pulp; Colchicum Autumnale Bulb; Helicobacter Pylori; Lactobacillus Acidophilus; Mercuric Chloride; Shigella Dysenteriae; Strychnos Nux-vomica Seed; Yersinia Enterocolitica
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]
Professional Complementary Health Formulas
Labeler Code:
63083
Product Label ID:
3b167c3e-10d2-4db1-881d-37f9101315fc
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
08-15-1984
Listing Expiration Date: [11]
12-31-2027
Exclude Flag: [12]
N
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Product Details

What is NDC 63083-9411?

The NDC code 63083-9411 is assigned by the FDA to the product Intestinal Nosode Combination 9411 which is a human over the counter drug product labeled by Professional Complementary Health Formulas. 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 63083-9411-1 29.5 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 Intestinal Nosode Combination 9411?

For the temporary relief of diarrhea, nausea or vomiting, minor abdominal pain or cramping, occasional headache, or lethargy.*

What are Intestinal Nosode Combination 9411 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.
  • ALOE 6 [hp_X]/29.5mL - A plant genus of the family ASPHODELACEAE which is used medicinally. It contains anthraquinone glycosides such as aloin-emodin or aloe-emodin (EMODIN).
  • CHOLERA ENTEROTOXIN SUBUNIT B 12 [hp_X]/29.5mL
  • CITRULLUS COLOCYNTHIS FRUIT PULP 6 [hp_X]/29.5mL
  • COLCHICUM AUTUMNALE BULB 4 [hp_X]/29.5mL
  • HELICOBACTER PYLORI 12 [hp_X]/29.5mL - A spiral bacterium active as a human gastric pathogen. It is a gram-negative, urease-positive, curved or slightly spiral organism initially isolated in 1982 from patients with lesions of gastritis or peptic ulcers in Western Australia. Helicobacter pylori was originally classified in the genus CAMPYLOBACTER, but RNA sequencing, cellular fatty acid profiles, growth patterns, and other taxonomic characteristics indicate that the micro-organism should be included in the genus HELICOBACTER. It has been officially transferred to Helicobacter gen. nov. (see Int J Syst Bacteriol 1989 Oct;39(4):297-405).
  • LACTOBACILLUS ACIDOPHILUS 12 [hp_X]/29.5mL - A species of gram-positive, rod-shaped bacteria isolated from the intestinal tract of humans and animals, the human mouth, and vagina. This organism produces the fermented product, acidophilus milk.
  • MERCURIC CHLORIDE 12 [hp_X]/29.5mL - Mercury chloride (HgCl2). A highly toxic compound that volatizes slightly at ordinary temperature and appreciably at 100 degrees C. It is corrosive to mucous membranes and used as a topical antiseptic and disinfectant.
  • SHIGELLA DYSENTERIAE 12 [hp_X]/29.5mL - A species of gram-negative, facultatively anaerobic, rod-shaped bacteria that is extremely pathogenic and causes severe dysentery. Infection with this organism often leads to ulceration of the intestinal epithelium.
  • STRYCHNOS NUX-VOMICA SEED 6 [hp_X]/29.5mL
  • YERSINIA ENTEROCOLITICA 14 [hp_X]/29.5mL - A species of the genus YERSINIA, isolated from both man and animal. It is a frequent cause of bacterial gastroenteritis in children.

Which are Intestinal Nosode Combination 9411 UNII Codes?

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

Which are Intestinal Nosode Combination 9411 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 Intestinal Nosode Combination 9411?

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

* Please review the disclaimer below.

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.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[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".