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  5. NDC Package Code: 17089-453-24 Guna-cough

NDC Package 17089-453-24 Guna-cough

Althaea Officinalis Leaf - Antimony Potassium Tartrate - Bryonia Alba Root - Cetraria - 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:
17089-453-24
Package Description:
1 BOTTLE in 1 BOX / 150 mL in 1 BOTTLE
Product Code:
17089-453
Proprietary Name:
Guna-cough
Non-Proprietary Name:
Althaea Officinalis Leaf - Antimony Potassium Tartrate - Bryonia Alba Root - Cetraria Islandica Subsp. Islandica - Cochineal - Copper - Drosera Rotundifolia - Echinacea Angustifolia - Garden Thyme - Lobaria Pulmonaria - Plantago Major -
Substance Name:
Althaea Officinalis Leaf; Antimony Potassium Tartrate; Bryonia Alba Root; Cetraria Islandica Subsp. Islandica; Cochineal; Copper; Drosera Rotundifolia; Echinacea Angustifolia; Lobaria Pulmonaria; Plantago Major; Thyme
Usage Information:
Use enclosed dosage cup for dosingAdults and children 12 years and older    10 ml  every 4 hours as neededChildren between 12 years and 2 years of age    5 ml  every 4 hours as neededChildren under 2 years     Ask a physician
11-Digit NDC Billing Format:
17089045324
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):
Pharmacologic Class(es):
Sample Package:
No
Marketing Category:
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date:
05-27-2010
Listing Expiration Date:
12-31-2025
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 17089-453-24?

The NDC Packaged Code 17089-453-24 is assigned to a package of 1 bottle in 1 box / 150 ml in 1 bottle of Guna-cough, 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 17089-453 included in the NDC Directory?

Yes, Guna-cough with product code 17089-453 is active and included in the NDC Directory. The product was first marketed by Guna Spa on May 27, 2010 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 17089-453-24?

The 11-digit format is 17089045324. 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
5-3-217089-453-245-4-217089-0453-24