Bone HP NDC 43406-0611

NDC codes

FDA NDC Directory

Product NDC (as listed)43406-0611Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43406-0611Add 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
43406-0611-1	43406061101	30 mL in 1 BOTTLE, DROPPER (43406-0611-1)Marketed from Jun 1, 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): Bone HP
Generic name (nonproprietary): sodium borate, oyster shell calcium carbonate crude, calcium fluoride, tribasic calcium phosphate, eupatorium perfoliatum flowering top, iron, hydrofluoric acid, hekla lava, toxicodendron pubescens leaf, ruta graveolens flowering top, silicon dioxide, comfrey root.
Active ingredients: Sodium borate — 30 [hp_C]/mLOyster shell calcium carbonate, Crude — 30 [hp_C]/mLCalcium fluoride — 30 [hp_C]/mLTribasic calcium phosphate — 30 [hp_C]/mLEupatorium perfoliatum flowering top — 30 [hp_C]/mLIron — 30 [hp_C]/mLHydrofluoric acid — 30 [hp_C]/mLHekla lava — 30 [hp_C]/mLToxicodendron pubescens leaf — 30 [hp_C]/mLRuta graveolens flowering top — 30 [hp_C]/mLSilicon dioxide — 30 [hp_C]/mLComfrey root — 30 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Natural Creations, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 1, 2016
Listing expires: Dec 31, 2026
Other FDA classes: Calcium (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Phosphate Chelating Activity (Mechanism)
Identifiers: Product ID 43406-0611_c32b90a6-ddf7-41d9-b6f3-2d808a8d9b93SPL ID c32b90a6-ddf7-41d9-b6f3-2d808a8d9b93SPL set ID 93d2b385-9ce3-4d16-b428-1638e9a55f92UNII 91MBZ8H3QO, 2E32821G6I, O3B55K4YKI, 91D9GV0Z28, 1W0775VX6E, E1UOL152H7, RGL5YE86CZ, C21158IIRK, 6IO182RP7A, N94C2U587S, ETJ7Z6XBU4, M9VVZ08EKQUPC 0877730004482
Pharmacologic class: Blood Coagulation Factor; 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

N443406061101 followed by a unit qualifier and the quantity

Package 43406-0611-01. 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 Nov 13, 2025.

Indications (excerpt from the label)

USES: Temporarily relieves bone aches and pains.**

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)