Neuroforce NDC 43857-0457

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0457Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0457Add 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
43857-0457-1	43857045701	30 mL in 1 BOTTLE, DROPPER (43857-0457-1)Marketed from Jul 28, 2017

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): Neuroforce
Generic name (nonproprietary): echinacea (angustifolia), hypericum perforatum, arnica montana, symphytum officinale, agaricus muscarius, arsenicum album, gelsemium sempervirens, plumbum metallicum, rhus tox
Active ingredients: Echinacea angustifolia — 3 [hp_X]/mLHypericum perforatum — 3 [hp_X]/mLArnica montana — 3 [hp_X]/mLComfrey root — 6 [hp_X]/mLAmanita muscaria fruiting body — 12 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLGelsemium sempervirens root — 12 [hp_X]/mLLead — 12 [hp_X]/mLToxicodendron pubescens leaf — 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: Jul 28, 2017
Listing expires: Dec 31, 2026
Identifiers: Product ID 43857-0457_c4c611f8-2d01-4a6f-8caa-a7e891f9e236SPL ID c4c611f8-2d01-4a6f-8caa-a7e891f9e236SPL set ID 328e1e3d-c411-413c-9a44-d0e41b7a9be4UNII VB06AV5US8, XK4IUX8MNB, O80TY208ZW, M9VVZ08EKQ, DIF093I037, S7V92P67HO, 639KR60Q1Q, 2P299V784P, 6IO182RP7A

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

N443857045701 followed by a unit qualifier and the quantity

Package 43857-0457-01. 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 Jul 28, 2017.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of minor burning pains and weakness and heaviness of the arms and legs; dull aching in lumbar and sacral regions of the back, passing upward and lightning-like pains in the back relieved temporarily by pressure.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)