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NDC 17089-470 Guna Bowel Plus

Activated Charcoal - Aloe - Aluminum Oxide - Bryonia Alba Root - Chelidonium Majus - - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 17089-470?
  4. Guna Bowel Plus 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) 17089-470 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:
17089-470
Proprietary Name:
Guna Bowel Plus
Non-Proprietary Name: [1]
Activated Charcoal - Aloe - Aluminum Oxide - Bryonia Alba Root - Chelidonium Majus - Collinsonia - Frangula Alnus Bark - Lycopodium Clavatum Spore - Potassium Carbonate- Rhubarb - Strychnos Nux Vomica Seed - Silybum Marianum Seed - Skatole - Sodium Carbonate - Sus Scrofa Pancreas - Taraxacum Officinale - Thiamine -
Substance Name: [2]
Activated Charcoal; Aloe; Aluminum Oxide; Bryonia Alba Root; Chelidonium Majus; Collinsonia; Frangula Alnus Bark; Lycopodium Clavatum Spore; Potassium Carbonate; Rhubarb; Silybum Marianum Seed; Skatole; Sodium Carbonate; Strychnos Nux-vomica Seed; Sus Scrofa Pancreas; Taraxacum Officinale; Thiamine
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.
Labeler Name: [5]
Guna Spa
Labeler Code:
17089
Product Label ID:
b3aa4fd3-c87a-ccd2-e053-2995a90a46a9
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
01-17-2021
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
N
Code Navigator:

Code Structure Chart

Product Details

What is NDC 17089-470?

The NDC code 17089-470 is assigned by the FDA to the product Guna Bowel Plus which is a human over the counter drug product labeled by Guna Spa. The generic name of Guna Bowel Plus is activated charcoal - aloe - aluminum oxide - bryonia alba root - chelidonium majus - collinsonia - frangula alnus bark - lycopodium clavatum spore - potassium carbonate- rhubarb - strychnos nux vomica seed - silybum marianum seed - skatole - sodium carbonate - sus scrofa pancreas - taraxacum officinale - thiamine -. The product's dosage form is solution/ drops and is administered via oral form. The product is distributed in a single package with assigned NDC code 17089-470-18 1 bottle, dropper in 1 box / 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 Guna Bowel Plus?

Take 15 minutes before meals

What are Guna Bowel Plus 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.

Which are Guna Bowel Plus UNII Codes?

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

Which are Guna Bowel Plus 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 Guna Bowel Plus?

* 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".