Mucus And Sinus Spray
NDC Package 17312-433-23

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Mucus And Sinus (bryonia alba, hydrastis canadensis, kali bichromicum, natrum muriaticum, pulsatilla pratensis, silicea, stannum metallicum, thuja occidentalis, zincum gluconicum) sprays is suitable for adults and children ages 12 and over. This formulation utilizes a spray delivery system. Marketed by Trp Company, this product is identified by NDC 17312-433.

Identification & Billing

NDC Package Code
17312-433-23
Package Description
1 BOTTLE, SPRAY in 1 CARTON / 20 mL in 1 BOTTLE, SPRAY
Product Code
17312-433
11-Digit Billing Format
17312043323

Clinical Specifications

Proprietary Name
Mucus And Sinus Mucus And Sinus Symptom Relief
Non-Proprietary Name
Bryonia Alba, Hydrastis Canadensis, Kali Bichromicum, Natrum Muriaticum, Pulsatilla Pratensis, Silicea, Stannum Metallicum, Thuja Occidentalis, Zincum Gluconicum
Substance Name
Bryonia Alba Root; Goldenseal; Potassium Dichromate; Pulsatilla Pratensis; Silicon Dioxide; Sodium Chloride; Thuja Occidentalis Leafy Twig; Tin; Zinc Gluconate
Dosage Form
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Suitable for adults and children ages 12 and over. Spray 2-3 times in mouth. • Keep in mouth for 15 seconds before swallowing. • Use up to 6 times a day as needed. • Use at least 10 minutes before or at least 10 minutes after eating or drinking. • Children under the age of 12: Consult a physician before use.

Regulatory & Marketing

Labeler Name
Trp Company
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
08-06-2024
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 17312-433-23 identifies a specific commercial package of 1 bottle, spray in 1 carton / 20 ml in 1 bottle, spray of Mucus And Sinus Mucus And Sinus Symptom Relief, a human over the counter drug labeled by Trp Company. This spray is formulated for oral use and contains bryonia alba root; goldenseal; potassium dichromate; pulsatilla pratensis; silicon dioxide; sodium chloride; thuja occidentalis leafy twig; tin; zinc gluconate as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Trp Company on August 06, 2024. The current certification is valid through December 31, 2026.

How is this Trp Company product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 17312043323. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
17312-433-23
11-Digit CMS (5-4-2)
17312-0433-23

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.