Bronchial Cough Liquid
NDC Package 43742-2034-1
Package Information
Bronchial Cough (coccus cacti, drosera (rotundifolia), scilla maritima, sticta pulmonaria, causticum, cuprum aceticum, arsenicum iodatum, carbo vegetabilis, kali carbonicum, lachesis mutus) liquids is for temporary relief of symptoms related to bronchial cough including irritating cough and congestion.**** These statements are based upon homeopathic principles. This formulation utilizes a liquid delivery system. Marketed by Deseret Biologicals, Inc., this product is identified by NDC 43742-2034.
Identification & Billing
Clinical Specifications
- ACTIVATED CHARCOAL 12 [hp_X]/mL
- ARSENIC TRIIODIDE 8 [hp_X]/mL
- CAUSTICUM 6 [hp_X]/mL
- CUPRIC ACETATE 6 [hp_X]/mL
- DRIMIA MARITIMA BULB 5 [hp_X]/mL
- DROSERA ROTUNDIFOLIA WHOLE 4 [hp_X]/mL
- LACHESIS MUTA VENOM 12 [hp_X]/mL
- LOBARIA PULMONARIA 4 [hp_X]/mL
- POTASSIUM CARBONATE 12 [hp_X]/mL
- PROTORTONIA CACTI 4 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 43742 - Deseret Biologicals, Inc.
- 43742-2034 - Bronchial Cough
- 43742-2034-1 - 30 mL in 1 BOTTLE, DROPPER
- 43742-2034 - Bronchial Cough
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 43742-2034-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Bronchial Cough, a human over the counter drug labeled by Deseret Biologicals, Inc.. This liquid is formulated for oral use and contains activated charcoal; arsenic triiodide; causticum; cupric acetate; drimia maritima bulb; drosera rotundifolia whole; lachesis muta venom; lobaria pulmonaria; potassium carbonate; protortonia cacti 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 Deseret Biologicals, Inc. on August 03, 2021. The current certification is valid through December 31, 2026.
How is this Deseret Biologicals, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 43742203401. 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:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.