Jointforce R Liquid
NDC Package 43857-0602-1
Package Information
Jointforce R (chondrus crispus, cimicifuga racemosa, spiraea ulmaria, trifolium pratense, urtica urens, xanthoxylum fraxineum, symphytum officinale, colchicum autumnale, ferrum phosphoricum, formica rufa, lithium carbonicum, natrum sulphuricum, rhododendron chrysanthemum, rhus tox) liquids is for temporary relief of pains throughout shoulder joint, arm, fingers, and small joints generally; swelling and tenderness of the finger and toe joints; and swellings in the joints with heat. This formulation utilizes a liquid delivery system. Marketed by Bioactive Nutritional, Inc., this product is identified by NDC 43857-0602.
Identification & Billing
Clinical Specifications
- BLACK COHOSH 3 [hp_X]/mL
- CHONDRUS CRISPUS 3 [hp_X]/mL
- COLCHICUM AUTUMNALE BULB 12 [hp_X]/mL
- COMFREY ROOT 6 [hp_X]/mL
- FERROSOFERRIC PHOSPHATE 12 [hp_X]/mL
- FILIPENDULA ULMARIA ROOT 9 [hp_X]/mL
- FORMICA RUFA 12 [hp_X]/mL
- LITHIUM CARBONATE 12 [hp_X]/mL
- RHODODENDRON AUREUM LEAF 12 [hp_X]/mL
- SODIUM SULFATE 12 [hp_X]/mL
- TOXICODENDRON PUBESCENS LEAF 12 [hp_X]/mL
- TRIFOLIUM PRATENSE FLOWER 3 [hp_X]/mL
- URTICA URENS WHOLE 3 [hp_X]/mL
- ZANTHOXYLUM AMERICANUM BARK 3 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 43857 - Bioactive Nutritional, Inc.
- 43857-0602 - Jointforce R
- 43857-0602-1 - 30 mL in 1 BOTTLE, DROPPER
- 43857-0602 - Jointforce R
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 43857-0602-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Jointforce R, a human over the counter drug labeled by Bioactive Nutritional, Inc.. This liquid is formulated for oral use and contains black cohosh; chondrus crispus; colchicum autumnale bulb; comfrey root; ferrosoferric phosphate; filipendula ulmaria root; formica rufa; lithium carbonate; rhododendron aureum leaf; sodium sulfate; toxicodendron pubescens leaf; trifolium pratense flower; urtica urens whole; zanthoxylum americanum bark 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 June 17, 2021. 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: 43857060201. 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.