Ld Force Hp Liquid
NDC Package 43857-0618-1
Package Information
Ld Force Hp (arsenicum album, borrelia burgdorferi nosode, chelidonium majus, coccus cacti, echinacea (angustifolia), hydrastis canadensis, lycopodium clavatum, nasturtium aquaticum, phosphorus, rhus tox, taraxacum officinale, thymus (suis), thyroidinum (suis), trifolium pratense, urtica dioica) liquids is for temporary relief of aches and pains of joints and muscles as a consequence of infection. This formulation utilizes a liquid delivery system. Marketed by Bioactive Nutritional, Inc., this product is identified by NDC 43857-0618.
Identification & Billing
Clinical Specifications
- ARSENIC TRIOXIDE 30 [hp_C]/mL
- BORRELIA BURGDORFERI 30 [hp_C]/mL
- CHELIDONIUM MAJUS WHOLE 30 [hp_C]/mL
- ECHINACEA ANGUSTIFOLIA WHOLE 30 [hp_C]/mL
- GOLDENSEAL 30 [hp_C]/mL
- LYCOPODIUM CLAVATUM SPORE 30 [hp_C]/mL
- NASTURTIUM OFFICINALE 30 [hp_C]/mL
- PHOSPHORUS 30 [hp_C]/mL
- PROTORTONIA CACTI 30 [hp_C]/mL
- SUS SCROFA THYMUS 30 [hp_C]/mL
- TARAXACUM OFFICINALE 30 [hp_C]/mL
- THYROID 30 [hp_C]/mL
- TOXICODENDRON PUBESCENS LEAF 30 [hp_C]/mL
- TRIFOLIUM PRATENSE FLOWER 30 [hp_C]/mL
- URTICA DIOICA WHOLE 30 [hp_C]/mL
Regulatory & Marketing
Hierarchy Structure
- 43857 - Bioactive Nutritional, Inc.
- 43857-0618 - Ld Force Hp
- 43857-0618-1 - 30 mL in 1 BOTTLE, DROPPER
- 43857-0618 - Ld Force 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 43857-0618-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Ld Force Hp, a human over the counter drug labeled by Bioactive Nutritional, Inc.. This liquid is formulated for oral use and contains arsenic trioxide; borrelia burgdorferi; chelidonium majus whole; echinacea angustifolia whole; goldenseal; lycopodium clavatum spore; nasturtium officinale; phosphorus; protortonia cacti; sus scrofa thymus; taraxacum officinale; thyroid; toxicodendron pubescens leaf; trifolium pratense flower; urtica dioica whole 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 November 08, 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: 43857061801. 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.