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  5. NDC Package Code: 17089-293-18 Guna-bowel

NDC Package 17089-293-18 Guna-bowel

Aloe - Aluminum Oxide - Bryonia Alba Root - Chelidonium Majus - Cholecalciferol - - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
17089-293-18
Package Description:
1 BOTTLE, DROPPER in 1 BOX / 30 mL in 1 BOTTLE, DROPPER
Product Code:
17089-293
Proprietary Name:
Guna-bowel
Non-Proprietary Name:
Aloe - Aluminum Oxide - Bryonia Alba Root - Chelidonium Majus - Cholecalciferol - Collinsonia - Frangula Alnus Bark - Niacin - Pantothenic Acid - Potassium Carbonate - Rhubarb - Silybum Marianum Seed - Skatole - Sodium Carbonate - Strychnos Nux-vomica Seed - Sus Scrofa Colon - Sus Scrofa Rectum - Taraxacum Officinale - Thiamine -
Substance Name:
Aloe; Aluminum Oxide; Bryonia Alba Root; Chelidonium Majus; Cholecalciferol; Collinsonia; Frangula Alnus Bark; Niacin; Pantothenic Acid; Potassium Carbonate; Rhubarb; Silybum Marianum Seed; Skatole; Sodium Carbonate; Strychnos Nux-vomica Seed; Sus Scrofa Colon; Sus Scrofa Rectum; Taraxacum Officinale; Thiamine
Usage Information:
Take 15 minutes before mealsAdults and children 12 years and older    20 drops in a little water, 2 times per dayChildren  between 12 years and 6 years of age    10 drops in a little water, 2 times per dayChildren under 6 years     5 drops in a glass of water, 2 times per day
11-Digit NDC Billing Format:
17089029318
Product Type:
Human Otc Drug
Labeler Name:
Guna Spa
Dosage Form:
Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ALOE 2 [hp_X]/30mL
  • ALUMINUM OXIDE 6 [hp_X]/30mL
  • BRYONIA ALBA ROOT 6 [hp_X]/30mL
  • CHELIDONIUM MAJUS 2 [hp_X]/30mL
  • CHOLECALCIFEROL 2 [hp_X]/30mL
  • COLLINSONIA 2 [hp_X]/30mL
  • FRANGULA ALNUS BARK 2 [hp_X]/30mL
  • NIACIN 2 [hp_X]/30mL
  • PANTOTHENIC ACID 2 [hp_X]/30mL
  • POTASSIUM CARBONATE 6 [hp_X]/30mL
  • RHUBARB 2 [hp_X]/30mL
  • SILYBUM MARIANUM SEED 2 [hp_X]/30mL
  • SKATOLE 10 [hp_X]/30mL
  • SODIUM CARBONATE 6 [hp_X]/30mL
  • STRYCHNOS NUX-VOMICA SEED 6 [hp_X]/30mL
  • SUS SCROFA COLON 12 [hp_X]/30mL
  • SUS SCROFA RECTUM 12 [hp_X]/30mL
  • TARAXACUM OFFICINALE 2 [hp_X]/30mL
  • THIAMINE 4 [hp_X]/30mL
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Allergens - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Dietary Proteins - [CS]
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Increased IgG Production - [PE] (Physiologic Effect)
  • Nicotinic Acid - [EPC] (Established Pharmacologic Class)
  • Nicotinic Acids - [CS]
  • Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Plant Proteins - [CS]
  • Seed Storage Proteins - [CS]
  • Vitamin D - [CS]
  • Vitamin D - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    05-23-2006
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 17089-293-18?

    The NDC Packaged Code 17089-293-18 is assigned to a package of 1 bottle, dropper in 1 box / 30 ml in 1 bottle, dropper of Guna-bowel, a human over the counter drug labeled by Guna Spa. The product's dosage form is solution/ drops and is administered via oral form.

    Is NDC 17089-293 included in the NDC Directory?

    Yes, Guna-bowel with product code 17089-293 is active and included in the NDC Directory. The product was first marketed by Guna Spa on May 23, 2006 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 17089-293-18?

    The 11-digit format is 17089029318. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-217089-293-185-4-217089-0293-18