Ligatone Liquid
NDC Package 43857-0001-1
Package Information
Ligatone (arnica montana, bryonia, calcarea phosphorica, causticum, kali carbonicum, manganese gluconate, mezereum, rhus tox, ruta graveolens, silicea) liquids is For temporary relief of painful lower back with burning, looseness of ligaments, general soreness, and aching tendons, ligaments, and bones. This formulation utilizes a liquid delivery system. Marketed by Bioactive Nutritional, Inc., this product is identified by NDC 43857-0001.
Identification & Billing
Clinical Specifications
- ARNICA MONTANA WHOLE 12 [hp_X]/mL
- BRYONIA ALBA ROOT 12 [hp_X]/mL
- CAUSTICUM 12 [hp_X]/mL
- DAPHNE MEZEREUM BARK 12 [hp_X]/mL
- MANGANESE GLUCONATE 12 [hp_X]/mL
- POTASSIUM CARBONATE 12 [hp_X]/mL
- RUTA GRAVEOLENS FLOWERING TOP 12 [hp_X]/mL
- SILICON DIOXIDE 12 [hp_X]/mL
- TOXICODENDRON PUBESCENS LEAF 12 [hp_X]/mL
- TRIBASIC CALCIUM PHOSPHATE 12 [hp_X]/mL
- Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
- Calcium - [CS]
- Cations, Divalent - [CS]
- Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
- Magnetic Resonance Contrast Activity - [MoA] (Mechanism of Action)
- Paramagnetic Contrast Agent - [EPC] (Established Pharmacologic Class)
- Phosphate Binder - [EPC] (Established Pharmacologic Class)
- Phosphate Chelating Activity - [MoA] (Mechanism of Action)
Regulatory & Marketing
Hierarchy Structure
- 43857 - Bioactive Nutritional, Inc.
- 43857-0001 - Ligatone
- 43857-0001-1 - 30 mL in 1 BOTTLE, DROPPER
- 43857-0001 - Ligatone
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 43857-0001-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Ligatone, a human over the counter drug labeled by Bioactive Nutritional, Inc.. This liquid is formulated for oral use and contains arnica montana whole; bryonia alba root; causticum; daphne mezereum bark; manganese gluconate; potassium carbonate; ruta graveolens flowering top; silicon dioxide; toxicodendron pubescens leaf; tribasic calcium phosphate 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 Bioactive Nutritional, Inc. on April 13, 2012. The current certification is valid through December 31, 2027.
How is this Bioactive Nutritional, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 43857000101. 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.