Traumatone NDC 44911-0416

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0416Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0416Add 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
44911-0416-1	44911041601	30 mL in 1 BOTTLE, DROPPER (44911-0416-1)Marketed from Feb 8, 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): Traumatone
Generic name (nonproprietary): calendula officinalis, symphytum officinale, arnica montana, bellis perennis, hypericum perforatum, ledum palustre, phosphorus, rhus tox, ruta graveolens, staphysagria, strontium carbonicum
Active ingredients: Calendula officinalis flowering top — 3 [hp_X]/mLComfrey root — 6 [hp_X]/mLArnica montana whole — 12 [hp_X]/mLBellis perennis whole — 12 [hp_X]/mLHypericum perforatum whole — 12 [hp_X]/mLRhododendron tomentosum leafy twig — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLToxicodendron pubescens leaf — 12 [hp_X]/mLRuta graveolens flowering top — 12 [hp_X]/mLDelphinium staphisagria seed — 12 [hp_X]/mLStrontium carbonate — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 8, 2017
Marketing end: Aug 30, 2027
Identifiers: Product ID 44911-0416_9df727b1-265a-48e3-ad50-feee3a962f3eSPL ID 9df727b1-265a-48e3-ad50-feee3a962f3eSPL set ID d4e72b3a-7336-410d-99e3-df10bcc65e75UNII 18E7415PXQ, M9VVZ08EKQ, O80TY208ZW, 2HU33I03UY, XK4IUX8MNB, 877L01IZ0P, 27YLU75U4W, 6IO182RP7A, N94C2U587S, 00543AP1JV, 41YPU4MMCAUPC 0363113700824

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

N444911041601 followed by a unit qualifier and the quantity

Package 44911-0416-01. 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 Aug 1, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve soreness after exertion, bruises, strains, sprains, and joint pain and stiffness.** **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)