Ligatone NDC 43857-0001

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0001Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0001Add 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
43857-0001-1	43857000101	30 mL in 1 BOTTLE, DROPPER (43857-0001-1)Marketed from Apr 14, 2016

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): Ligatone
Generic name (nonproprietary): arnica montana, bryonia, calcarea phosphorica, causticum, kali carbonicum, manganese gluconate, mezereum, rhus tox, ruta graveolens, silicea
Active ingredients: Arnica montana whole — 12 [hp_X]/mLBryonia alba root — 12 [hp_X]/mLTribasic calcium phosphate — 12 [hp_X]/mLCausticum — 12 [hp_X]/mLPotassium carbonate — 12 [hp_X]/mLManganese gluconate — 12 [hp_X]/mLDaphne mezereum bark — 12 [hp_X]/mLToxicodendron pubescens leaf — 12 [hp_X]/mLRuta graveolens flowering top — 12 [hp_X]/mLSilicon dioxide — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Apr 13, 2012
Listing expires: Dec 31, 2027
Other FDA classes: Calcium (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Magnetic Resonance Contrast Activity (Mechanism)Phosphate Chelating Activity (Mechanism)
Identifiers: Product ID 43857-0001_96833ba7-cf09-4188-9707-2e2b52328bfbSPL ID 96833ba7-cf09-4188-9707-2e2b52328bfbSPL set ID 3a3bdd55-daec-43b9-a380-54a747fb7d10UNII O80TY208ZW, T7J046YI2B, 91D9GV0Z28, DD5FO1WKFU, BQN1B9B9HA, 9YY2F980SV, X2N6E405GV, 6IO182RP7A, N94C2U587S, ETJ7Z6XBU4UPC 0210184341596
Pharmacologic class: Blood Coagulation Factor; Paramagnetic Contrast Agent; Phosphate Binder

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

N443857000101 followed by a unit qualifier and the quantity

Package 43857-0001-01. 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 13, 2026.

Indications (excerpt from the label)

USES: For temporary relief of painful low back with burning, looseness of ligaments and general soreness and aching tendons, ligaments, and bones.** **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)