NDC Package 17089-470-18 Guna Bowel Plus

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

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:
17089-470-18
Package Description:
1 BOTTLE, DROPPER in 1 BOX / 30 mL in 1 BOTTLE, DROPPER
Product Code:
Proprietary Name:
Guna Bowel Plus
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 -
Substance Name:
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
Usage Information:
Take 15 minutes before meals
11-Digit NDC Billing Format:
17089047018
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.
  • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    01-17-2021
    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 17089-470-18?

    The NDC Packaged Code 17089-470-18 is assigned to a package of 1 bottle, dropper in 1 box / 30 ml in 1 bottle, dropper of Guna Bowel Plus, 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 17089-470 included in the NDC Directory?

    Yes, Guna Bowel Plus with product code 17089-470 is active and included in the NDC Directory. The product was first marketed by Guna Spa on January 17, 2021 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 17089-470-18?

    The 11-digit format is 17089047018. 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
    5-3-217089-470-185-4-217089-0470-18