What is NDC 43857-0593?

43857-0593 is the product NDC for Dentox, Berberis vulgaris root bark 3 [hp_X]/mL + 24 more ingredients liquid, listed with the FDA by BioActive Nutritional, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

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).

What is the active ingredient?

Berberis vulgaris root bark, Glycyrrhiza glabra, Arctium lappa root, Stillingia sylvatica root, Trifolium pratense flower, Phytolacca americana root, Sus scrofa lymph, Sus scrofa bone marrow, Sus scrofa thymus, Thyroid, Calcium fluoride, Sodium fluoride, Silver, Gold, Copper, Eugenol, Formaldehyde solution, Lidocaine, Mercurius solubilis, Molybdenum, Nickel, Palladium, Tin, Titanium, Zinc.

BioActive Nutritional, Inc., NDC labeler code 43857. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Dentox?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Dentox NDC 43857-0593 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0593Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0593Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
43857-0593-1	4385705930143857059301	30 mL in 1 BOTTLE, DROPPER (43857-0593-1)Marketed from Feb 14, 2023

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Dentox
Generic name (nonproprietary): 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
Active ingredients: Berberis vulgaris root bark — 3 [hp_X]/mLGlycyrrhiza glabra — 3 [hp_X]/mLArctium lappa root — 3 [hp_X]/mLStillingia sylvatica root — 3 [hp_X]/mLTrifolium pratense flower — 3 [hp_X]/mLPhytolacca americana root — 4 [hp_X]/mLSus scrofa lymph — 8 [hp_X]/mLSus scrofa bone marrow — 8 [hp_X]/mLSus scrofa thymus — 8 [hp_X]/mLThyroid — 8 [hp_X]/mLCalcium fluoride — 12 [hp_X]/mLSodium fluoride — 12 [hp_X]/mLSilver — 12 [hp_X]/mLGold — 12 [hp_X]/mLCopper — 12 [hp_X]/mLEugenol — 12 [hp_X]/mLFormaldehyde solution — 12 [hp_X]/mLLidocaine — 12 [hp_X]/mLMercurius solubilis — 12 [hp_X]/mLMolybdenum — 12 [hp_X]/mLNickel — 12 [hp_X]/mLPalladium — 12 [hp_X]/mLTin — 12 [hp_X]/mLTitanium — 12 [hp_X]/mLZinc — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.NDC labeler code 43857
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 14, 2023
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Amides (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)Local Anesthesia (Physiologic effect)Plant Proteins (Chemical structure)
Identifiers: Product ID 43857-0593_dc063355-9747-4133-b7be-beebc2333e11SPL ID dc063355-9747-4133-b7be-beebc2333e11SPL set ID dbe965b3-e81e-4328-bc41-43e875e12a05UNII 1TH8Q20J0U, 2788Z9758H, 597E9BI3Z3, QBR70R4FBK, 4JS0838828, 11E6VI8VEG, 33A7VYU29L, VP2CN2G7Y8, 7B69B0BD62, 6RV024OAUQ, O3B55K4YKI, 8ZYQ1474W7, 3M4G523W1G, 79Y1949PYO, 789U1901C5, 3T8H1794QW, T0H3L6C7I5, 98PI200987, 324Y4038G2, 81AH48963U, 7OV03QG267, 5TWQ1V240M, 387GMG9FH5, D1JT611TNE, J41CSQ7QDS
Pharmacologic class: Amide Local Anesthetic; Antiarrhythmic; Copper-containing Intrauterine Device; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Standardized Chemical Allergen

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N443857059301 followed by a unit qualifier and the quantity

Package 43857-0593-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Mar 18, 2026.

Indications (excerpt from the label)

USES: For temporary relief of pain and minor inflammation in the mouth or on the gums following dental procedures.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 43857-0593

What is NDC 43857-0593?: 43857-0593 is the product NDC for Dentox, Berberis vulgaris root bark 3 [hp_X]/mL + 24 more ingredients liquid, listed with the FDA by BioActive Nutritional, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: 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).
What is the active ingredient?: Berberis vulgaris root bark, Glycyrrhiza glabra, Arctium lappa root, Stillingia sylvatica root, Trifolium pratense flower, Phytolacca americana root, Sus scrofa lymph, Sus scrofa bone marrow, Sus scrofa thymus, Thyroid, Calcium fluoride, Sodium fluoride, Silver, Gold, Copper, Eugenol, Formaldehyde solution, Lidocaine, Mercurius solubilis, Molybdenum, Nickel, Palladium, Tin, Titanium, Zinc.
Who is the labeler?: BioActive Nutritional, Inc., NDC labeler code 43857. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Dentox?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.