Trauma plus Gel NDC 44911-0466

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0466Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0466Add 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
44911-0466-1	44911046601	57 g in 1 TUBE (44911-0466-1)Marketed from Aug 20, 2018

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): Trauma plus Gel
Generic name (nonproprietary): calendula officinalis, arnica montana, hypericum perforatum, symphytum officinale, bellis perennis, ledum palustre, sulphuricum acidum, calcarea fluorica, ferrum phosphoricum, rhus tox, ruta graveolens, natrum sulphuricum
Active ingredients: Calendula officinalis flowering top — 1 [hp_X]/gArnica montana — 1 [hp_X]/gHypericum perforatum — 1 [hp_X]/gComfrey root — 6 [hp_X]/gBellis perennis — 12 [hp_X]/gLedum palustre twig — 12 [hp_X]/gSulfuric acid — 12 [hp_X]/gCalcium fluoride — 30 [hp_X]/gFerrosoferric phosphate — 30 [hp_X]/gToxicodendron pubescens leaf — 30 [hp_X]/gRuta graveolens flowering top — 30 [hp_X]/gSodium sulfate — 30 [hp_C]/g
Dosage form: Gel
Route: Topical
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 20, 2018
Marketing end: Jan 5, 2031
Identifiers: Product ID 44911-0466_99572f2b-6667-460a-828f-2074e823f91fSPL ID 99572f2b-6667-460a-828f-2074e823f91fSPL set ID 53f4232b-23d4-48dc-aa76-175fdebfc74fUNII 18E7415PXQ, O80TY208ZW, XK4IUX8MNB, M9VVZ08EKQ, 2HU33I03UY, 877L01IZ0P, O40UQP6WCF, O3B55K4YKI, 91GQH8I5F7, 6IO182RP7A, N94C2U587S, 0YPR65R21J

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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N444911046601 followed by a unit qualifier and the quantity

Package 44911-0466-01. 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 May 6, 2026.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve pain associated with bumps, bruises, abrasions, strains, sprains, fractures, stiffness; for all minor injuries.** **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)