Cough Plus Bronchial Spray
NDC Package 50845-0246-1

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

Package Information

Cough Plus Bronchial (antimonium tartaricum, arum triphyllum, badiaga, baptisia tinctoria, bryonia (alba), drosera (rotundifolia), echinacea (angustifolia), eupatorium perfoliatum, kali bromatum, lung suis, phosphorus, pulsatilla (pratensis), spongia tosta, sticta pulmonaria, sulphur iodatum, urtica urens) sprays is adults and children over 12 Spray twice under the tongue three times per day. This formulation utilizes a spray delivery system. Marketed by Liddell Laboratories, Inc., this product is identified by NDC 50845-0246.

Identification & Billing

NDC Package Code
50845-0246-1
Package Description
30 mL in 1 BOTTLE, SPRAY
Product Code
50845-0246
11-Digit Billing Format
50845024601

Clinical Specifications

Proprietary Name
Cough Plus Bronchial
Non-Proprietary Name
Antimonium Tartaricum, Arum Triphyllum, Badiaga, Baptisia Tinctoria, Bryonia (alba), Drosera (rotundifolia), Echinacea (angustifolia), Eupatorium Perfoliatum, Kali Bromatum, Lung Suis, Phosphorus, Pulsatilla (pratensis), Spongia Tosta, Sticta Pulmonaria, Sulphur Iodatum, Urtica Urens
Substance Name
Antimony Potassium Tartrate; Arisaema Triphyllum Root; Baptisia Tinctoria Root; Bryonia Alba Root; Drosera Rotundifolia Whole; Echinacea Angustifolia Whole; Eupatorium Perfoliatum Flowering Top; Lobaria Pulmonaria; Phosphorus; Potassium Bromide; Pulsatilla Pratensis Whole; Silicon Dioxide; Spongia Officinalis Skeleton, Roasted; Spongilla Lacustris; Sulfur Iodide; Sus Scrofa Lung; Urtica Urens Whole
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)
Usage Information
Adults and children over 12 Spray twice under the tongue three times per day. For severe symptoms, dosage may be taken up to six times the first day.Children 12 and under Consult a doctor prior to use.

Regulatory & Marketing

Labeler Name
Liddell Laboratories, Inc.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
04-09-2019
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 50845-0246-1 identifies a specific commercial package of 30 ml in 1 bottle, spray of Cough Plus Bronchial, a human over the counter drug labeled by Liddell Laboratories, Inc.. This spray is formulated for oral use and contains antimony potassium tartrate; arisaema triphyllum root; baptisia tinctoria root; bryonia alba root; drosera rotundifolia whole; echinacea angustifolia whole; eupatorium perfoliatum flowering top; lobaria pulmonaria; phosphorus; potassium bromide; pulsatilla pratensis whole; silicon dioxide; spongia officinalis skeleton, roasted; spongilla lacustris; sulfur iodide; sus scrofa lung; urtica urens whole 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 Liddell Laboratories, Inc. on April 09, 2019. The current certification is valid through December 31, 2026.

How is this Liddell Laboratories, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 50845024601. 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 (5-4-1)
50845-0246-1
11-Digit CMS (5-4-2)
50845-0246-01

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