Cough Liquid
NDC Package 44911-0319-1
Package Information
Cough (arsenicum album, bryonia (alba), corallium rubrum, cuprum aceticum, drosera (rotundifolia), ipecacuanha, kali carbonicum, phosphorus, pulsatilla (pratensis), spongia tosta) liquids May temporarily relieve symptoms associated with chronic chest congestion, irritation, tickling, and cough with smarting in the chest.****Claims based on traditional homeopathic practice, not accepted medical evidence. This formulation utilizes a liquid delivery system. Marketed by Energique, Inc., this product is identified by NDC 44911-0319.
Identification & Billing
Clinical Specifications
- ARSENIC TRIOXIDE 30 [hp_X]/mL
- BRYONIA ALBA ROOT 30 [hp_X]/mL
- CORALLIUM RUBRUM EXOSKELETON 30 [hp_X]/mL
- CUPRIC ACETATE 30 [hp_X]/mL
- DROSERA ROTUNDIFOLIA WHOLE 30 [hp_X]/mL
- IPECAC 30 [hp_X]/mL
- PHOSPHORUS 30 [hp_X]/mL
- POTASSIUM CARBONATE 30 [hp_X]/mL
- PULSATILLA PRATENSIS WHOLE 30 [hp_X]/mL
- SPONGIA OFFICINALIS SKELETON, ROASTED 30 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 44911 - Energique, Inc.
- 44911-0319 - Cough
- 44911-0319-1 - 30 mL in 1 BOTTLE, DROPPER
- 44911-0319 - 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.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 44911-0319-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Cough HP, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains arsenic trioxide; bryonia alba root; corallium rubrum exoskeleton; cupric acetate; drosera rotundifolia whole; ipecac; phosphorus; potassium carbonate; pulsatilla pratensis whole; spongia officinalis skeleton, roasted 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 Energique, Inc. on January 12, 2016. The current certification is valid through December 31, 2026.
How is this Energique, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 44911031901. 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.