Upper Resp Hp Liquid
NDC Package 44911-0595-1
Package Information
Upper Resp Hp (carbo vegetabilis, cuprum metallicum, drosera (rotundifolia), hepar sulphuris calcareum, ipecacuanha, lachesis mutus, lobelia inflata, phosphorus, pulsatilla (pratensis), rumex crispus, spongia tosta) liquids May temporarily relieve symptoms of chronic cough, heaviness in chest, and bronchial irritation.****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 44911-0595.
Identification & Billing
Clinical Specifications
- ACTIVATED CHARCOAL 30 [hp_X]/mL
- CALCIUM SULFIDE 30 [hp_X]/mL
- COPPER 30 [hp_X]/mL
- DROSERA ROTUNDIFOLIA WHOLE 30 [hp_X]/mL
- IPECAC 30 [hp_X]/mL
- LACHESIS MUTA VENOM 30 [hp_X]/mL
- LOBELIA INFLATA WHOLE 30 [hp_X]/mL
- PHOSPHORUS 30 [hp_X]/mL
- PULSATILLA PRATENSIS WHOLE 30 [hp_X]/mL
- RUMEX CRISPUS ROOT 30 [hp_X]/mL
- SPONGIA OFFICINALIS SKELETON, ROASTED 30 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 44911 - Energique, Inc.
- 44911-0595 - Upper Resp Hp
- 44911-0595-1 - 30 mL in 1 BOTTLE, DROPPER
- 44911-0595 - Upper Resp Hp
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 44911-0595-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Upper Resp Hp, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains activated charcoal; calcium sulfide; copper; drosera rotundifolia whole; ipecac; lachesis muta venom; lobelia inflata whole; phosphorus; pulsatilla pratensis whole; rumex crispus root; 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 04, 2021. 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: 44911059501. 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.