Joint Hp Liquid
NDC Package 44911-0585-1
Package Information
Joint Hp (apis mellifica, bryonia (alba), causticum, colchicum autumnale, kali carbonicum, kalmia latifolia, ledum palustre, pulsatilla (pratensis), rhododendron chrysanthum, rhus tox) liquids May temporarily relieve symptoms due to minor joint inflammation and swelling.****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 44911-0585.
Identification & Billing
Clinical Specifications
- APIS MELLIFERA 30 [hp_X]/mL
- BRYONIA ALBA ROOT 30 [hp_X]/mL
- CAUSTICUM 30 [hp_X]/mL
- COLCHICUM AUTUMNALE BULB 30 [hp_X]/mL
- KALMIA LATIFOLIA LEAF 30 [hp_X]/mL
- LEDUM PALUSTRE TWIG 30 [hp_X]/mL
- POTASSIUM CARBONATE 30 [hp_X]/mL
- PULSATILLA PRATENSIS WHOLE 30 [hp_X]/mL
- RHODODENDRON AUREUM LEAF 30 [hp_X]/mL
- TOXICODENDRON PUBESCENS LEAF 30 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 44911 - Energique, Inc.
- 44911-0585 - Joint Hp
- 44911-0585-1 - 30 mL in 1 BOTTLE, DROPPER
- 44911-0585 - Joint 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.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 44911-0585-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Joint Hp, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains apis mellifera; bryonia alba root; causticum; colchicum autumnale bulb; kalmia latifolia leaf; ledum palustre twig; potassium carbonate; pulsatilla pratensis whole; rhododendron aureum leaf; toxicodendron pubescens leaf 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 May 24, 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: 44911058501. 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.