Jointstat Bb Liquid
NDC Package 44911-0729-1
Package Information
Jointstat Bb (chelidonium majus, echinacea (angustifolia), hydrastis canadensis, arsenicum album, bryonia (alba), colchicum autumnale, kalmia latifolia, ledum palustre, lycopodium clavatum, phosphorus, rhus tox) liquids is • Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional.• Consult a physician for use in children under 12 years of age. This formulation utilizes a liquid delivery system. Marketed by Energique, Inc., this product is identified by NDC 44911-0729.
Identification & Billing
Clinical Specifications
- ARSENIC TRIOXIDE 12 [hp_X]/mL
- BRYONIA ALBA ROOT 12 [hp_X]/mL
- CHELIDONIUM MAJUS WHOLE 3 [hp_X]/mL
- COLCHICUM AUTUMNALE BULB 12 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA WHOLE 3 [hp_X]/mL
- GOLDENSEAL 6 [hp_X]/mL
- KALMIA LATIFOLIA LEAF 12 [hp_X]/mL
- LACHESIS MUTA VENOM 12 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
- PHOSPHORUS 12 [hp_X]/mL
- PHYTOLACCA AMERICANA ROOT 4 [hp_X]/mL
- RHODODENDRON TOMENTOSUM LEAFY TWIG 12 [hp_X]/mL
- SMILAX ORNATA ROOT 12 [hp_X]/mL
- TOXICODENDRON PUBESCENS LEAF 12 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 44911 - Energique, Inc.
- 44911-0729 - Jointstat Bb
- 44911-0729-1 - 30 mL in 1 BOTTLE, DROPPER
- 44911-0729 - Jointstat Bb
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 44911-0729-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Jointstat Bb, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains arsenic trioxide; bryonia alba root; chelidonium majus whole; colchicum autumnale bulb; echinacea angustifolia whole; goldenseal; kalmia latifolia leaf; lachesis muta venom; lycopodium clavatum spore; phosphorus; phytolacca americana root; rhododendron tomentosum leafy twig; smilax ornata root; 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 January 27, 2025. 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: 44911072901. 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.