Osteoplex NDC 43857-0555

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0555Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0555Add 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
43857-0555-1	43857055501	30 mL in 1 BOTTLE, DROPPER (43857-0555-1)Marketed from Jul 15, 2020

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): Osteoplex
Generic name (nonproprietary): equisetum hyemale, magnesia muriatica, ascorbicum acidum, manganum muriaticum, symphytum officinale, medulla ossis suis, calcarea fluorica, calcarea phosphorica, silicea, parathyroid gland (suis), ligament (suis)
Active ingredients: Equisetum hyemale whole — 3 [hp_X]/mLMagnesium chloride — 3 [hp_X]/mLAscorbic acid — 6 [hp_X]/mLManganese chloride — 6 [hp_X]/mLComfrey root — 6 [hp_X]/mLSus scrofa bone marrow — 8 [hp_X]/mLCalcium fluoride — 12 [hp_X]/mLTribasic calcium phosphate — 12 [hp_X]/mLSilicon dioxide — 12 [hp_X]/mLSus scrofa parathyroid gland — 8 [hp_C]/mLSus scrofa ligament — 30 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 15, 2020
Listing expires: Dec 31, 2027
Other FDA classes: Ascorbic Acid (Chemical structure)Calcium (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Magnetic Resonance Contrast Activity (Mechanism)Osmotic Activity (Mechanism)Phosphate Chelating Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 43857-0555_d22123dd-aaad-4b98-b8ec-813ebfdb656eSPL ID d22123dd-aaad-4b98-b8ec-813ebfdb656eSPL set ID 8a7e1397-a387-4f2c-ab4f-7f1a7f1a849bUNII 59677RXH25, 02F3473H9O, PQ6CK8PD0R, QQE170PANO, M9VVZ08EKQ, VP2CN2G7Y8, O3B55K4YKI, 91D9GV0Z28, ETJ7Z6XBU4, 2KBE35NE8S, 2004Q810JOUPC 0810184340478
Pharmacologic class: Blood Coagulation Factor; Calculi Dissolution Agent; Osmotic Laxative; Paramagnetic Contrast Agent; Phosphate Binder; Vitamin C

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

N443857055501 followed by a unit qualifier and the quantity

Package 43857-0555-01. 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 5, 2026.

Indications (excerpt from the label)

USES: For temporary relief of pain in lower part of the back with burning, chronic lower back pain, soreness in the sacroiliac area, pain in the joints & 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)