Dentox Liquid
NDC Package 43857-0593-1
Package Information
Dentox (berberis vulgaris, glycyrrhiza glabra, lappa major, stillingia sylvatica, trifolium pratense, phytolacca decandra, lymph node(suis), medulla ossis suis, thymus (suis), thyroidinum (suis), calcarea fluorica, natrum fluoratum, argentum metallicum, aurum metallicum, cuprum metallicum, eugenol, formalinum, lidocaine, mercurius solubilis, molybdenum, niccolum metallicum, palladium metallicum, stannum metallicum, titanium metallicum, zincum metallicum) liquids is 10 drops orally, 3 times a day. This formulation utilizes a liquid delivery system. Marketed by Bioactive Nutritional, Inc., this product is identified by NDC 43857-0593.
Identification & Billing
Clinical Specifications
- ARCTIUM LAPPA ROOT 3 [hp_X]/mL
- BERBERIS VULGARIS ROOT BARK 3 [hp_X]/mL
- CALCIUM FLUORIDE 12 [hp_X]/mL
- COPPER 12 [hp_X]/mL
- EUGENOL 12 [hp_X]/mL
- FORMALDEHYDE SOLUTION 12 [hp_X]/mL
- GLYCYRRHIZA GLABRA 3 [hp_X]/mL
- GOLD 12 [hp_X]/mL
- LIDOCAINE 12 [hp_X]/mL
- MERCURIUS SOLUBILIS 12 [hp_X]/mL
- MOLYBDENUM 12 [hp_X]/mL
- NICKEL 12 [hp_X]/mL
- PALLADIUM 12 [hp_X]/mL
- PHYTOLACCA AMERICANA ROOT 4 [hp_X]/mL
- SILVER 12 [hp_X]/mL
- SODIUM FLUORIDE 12 [hp_X]/mL
- STILLINGIA SYLVATICA ROOT 3 [hp_X]/mL
- SUS SCROFA BONE MARROW 8 [hp_X]/mL
- SUS SCROFA LYMPH 8 [hp_X]/mL
- SUS SCROFA THYMUS 8 [hp_X]/mL
- THYROID 8 [hp_X]/mL
- TIN 12 [hp_X]/mL
- TITANIUM 12 [hp_X]/mL
- TRIFOLIUM PRATENSE FLOWER 3 [hp_X]/mL
- ZINC 12 [hp_X]/mL
- Allergens - [CS]
- Allergens - [CS]
- Amide Local Anesthetic - [EPC] (Established Pharmacologic Class)
- Amides - [CS]
- Antiarrhythmic - [EPC] (Established Pharmacologic Class)
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Copper - [CS]
- Copper-containing Intrauterine Device - [EPC] (Established Pharmacologic Class)
- Decreased Embryonic Implantation - [PE] (Physiologic Effect)
- Decreased Sperm Motility - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Inhibit Ovum Fertilization - [PE] (Physiologic Effect)
- Local Anesthesia - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
Regulatory & Marketing
Hierarchy Structure
- 43857 - Bioactive Nutritional, Inc.
- 43857-0593 - Dentox
- 43857-0593-1 - 30 mL in 1 BOTTLE, DROPPER
- 43857-0593 - Dentox
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.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 43857-0593-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Dentox, a human over the counter drug labeled by Bioactive Nutritional, Inc.. This liquid is formulated for oral use and contains arctium lappa root; berberis vulgaris root bark; calcium fluoride; copper; eugenol; formaldehyde solution; glycyrrhiza glabra; gold; lidocaine; mercurius solubilis; molybdenum; nickel; palladium; phytolacca americana root; silver; sodium fluoride; stillingia sylvatica root; sus scrofa bone marrow; sus scrofa lymph; sus scrofa thymus; thyroid; tin; titanium; trifolium pratense flower; zinc 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 February 14, 2023. 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: 43857059301. 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.