Calciforce Liquid
NDC Package 43857-0569-1
Package Information
Calciforce (arnica montana, chamomilla, echinacea (angustifolia), boron citrate, symphytum officinale, calcarea fluorica, calcarea phosphorica, hekla lava, lycopodium clavatum, silicea, calcarea carbonica) liquids is for temporary relief of tickling cough troublesome at night, pains in joints & bones, cramps in calves and soles. This formulation utilizes a liquid delivery system. Marketed by Bioactive Nutritional, Inc., this product is identified by NDC 43857-0569.
Identification & Billing
Clinical Specifications
- ARNICA MONTANA WHOLE 3 [hp_X]/mL
- BORON CITRATE 6 [hp_X]/mL
- CALCIUM FLUORIDE 12 [hp_X]/mL
- COMFREY ROOT 6 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA WHOLE 3 [hp_X]/mL
- HEKLA LAVA 12 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
- MATRICARIA CHAMOMILLA WHOLE 3 [hp_X]/mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_X]/mL
- SILICON DIOXIDE 12 [hp_X]/mL
- TRIBASIC CALCIUM PHOSPHATE 12 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 43857 - Bioactive Nutritional, Inc.
- 43857-0569 - Calciforce
- 43857-0569-1 - 30 mL in 1 BOTTLE, DROPPER
- 43857-0569 - Calciforce
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 43857-0569-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Calciforce, a human over the counter drug labeled by Bioactive Nutritional, Inc.. This liquid is formulated for oral use and contains arnica montana whole; boron citrate; calcium fluoride; comfrey root; echinacea angustifolia whole; hekla lava; lycopodium clavatum spore; matricaria chamomilla whole; oyster shell calcium carbonate, crude; silicon dioxide; 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 January 04, 2021. The current certification is valid through December 31, 2026.
How is this Bioactive Nutritional, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 43857056901. 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.