NDC 17089-470 Guna Bowel Plus

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 -

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  3. NDC: 17089-470 Guna Bowel Plus

NDC Product Code 17089-470

NDC CODE: 17089-470

Proprietary Name: Guna Bowel Plus What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: 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 - 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.
  • Drug uses not available

NDC Code Structure

NDC 17089-470-18

Package Description: 1 BOTTLE, DROPPER in 1 BOX > 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Guna Bowel Plus with NDC 17089-470 is a 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.

Labeler Name: Guna Spa

Dosage Form: Solution/ Drops - A solution which is usually administered in a drop-wise fashion.

Product Type: Human Otc Drug 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.

Guna Bowel Plus Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
  • ALOE 4 [hp_X]/30mL
  • ALUMINUM OXIDE 6 [hp_X]/30mL
  • BRYONIA ALBA ROOT 6 [hp_X]/30mL
  • SILYBUM MARIANUM SEED 2 [hp_X]/30mL
  • CHELIDONIUM MAJUS 2 [hp_X]/30mL
  • ACTIVATED CHARCOAL 6 [hp_X]/30mL
  • COLLINSONIA 2 [hp_X]/30mL
  • SUS SCROFA PANCREAS 6 [hp_X]/30mL
  • POTASSIUM CARBONATE 6 [hp_X]/30mL
  • SODIUM CARBONATE 6 [hp_X]/30mL
  • LYCOPODIUM CLAVATUM SPORE 2 [hp_X]/30mL
  • STRYCHNOS NUX-VOMICA SEED 6 [hp_X]/30mL
  • FRANGULA ALNUS BARK 2 [hp_X]/30mL
  • RHUBARB 2 [hp_X]/30mL
  • SKATOLE 6 [hp_X]/30mL
  • TARAXACUM OFFICINALE 2 [hp_X]/30mL
  • THIAMINE 4 [hp_X]/30mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.
  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.
  • Oral - Administration to or by way of the mouth.

Product Labeler Information

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

Labeler Name: Guna Spa
Labeler Code: 17089
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.
Start Marketing Date: 01-17-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2022 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.
Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Guna Bowel Plus Product Label Images

Guna Bowel Plus Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Indications & Usage

Take 15 minutes before meals

Inactive Ingredient

Inactive ingredient: Ethyl alcohol 30%

Questions

Questions?: info@gunainc.com, tel. (484) 223-3500

Directions

Adults and children 12 years and older 20 drops in a little water, 2 times per day

Children between 12 years and 6 years of age 10 drops in a little water, 2 times per day

Children under 6 years: consulta a physician

Warnings

Keep out of reach of children

  • Stop use and ask doctor if symptoms persist more than 5 days.
  • If pregnant or breast-feeding ask a health care professional before use.
  • Keep out of reach of children. In case of accidental overdose, seek professional assitance ot or contact a Poison Control Center immediately
  • Contains Aloe: do not use orally for more than 30 days.Contains ethyl alcohol 30%

Pregnancy

If pregnant or breast-feeding ask a health care professional before use

Uses

  • Temporary relief of gastrointestinal disorders, such as:constipationnauseaabdominal gasimpaired digestion

Active Ingredients/Purpose

Aloe 4X Relieves constipationAlumina 6X, 8X Relieves constipationBryonia 6X, 8X Relieves nausea, appetite disordersCarbo vegetabilis 6X Helps digestionCarduus marianus 2X Supports liver functionChelidonium majus 2X Supports liver and gallbladder functionCollinsonia canadensis 2X Relieves hemorrhoids and constipationKali carbonicum 6X, 8X, 12X Relieves abdominal gas and nauseaLycopodium clavatum 2X Supports liver function and drainageNatrum carbonicum 6X, 8X, 12X Helps digestionNux vomica 6X, 8X Relieves abdominal gas and helps digestionPancreas suis 6X Relieves nausea, appetite disordersRhamnus frangula 2X Relieves nauseaRheum 2X Relieves constipationSkatolum 6X, 10X Helps digestionTaraxacum officinale 2X Supports liver and gallbladder functionThiaminum hydroc. 4X Relieves abdominal gas and helps digestion

* Please review the disclaimer below.