Traumex NDC 62795-2302

NDC codes

FDA NDC Directory

Product NDC (as listed)62795-2302Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62795-2302Add 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
62795-2302-2	62795230202	60 TABLET, CHEWABLE in 1 BOTTLE (62795-2302-2)Marketed from Mar 20, 2023

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): Traumex
Generic name (nonproprietary): arnica montana whole, calendula officinalis flowering top, hamamelis virginiana root bark/stem bark,baptisia tinctoria root, bellis perennis whole, echinacea angustifolia whole,aconitum napellus whole,matricaria chamomilla whole,achillea millefolium whole,atropa belladonna,hypericum perforatum whole,ruta graveolens flowering top and comfrey root
Active ingredients: Arnica montana whole — 3 [hp_X]/1Calendula officinalis flowering top — 2 [hp_X]/1Hamamelis virginiana root bark/stem bark — 2 [hp_X]/1Baptisia tinctoria root — 2 [hp_X]/1Bellis perennis whole — 2 [hp_X]/1Echinacea angustifolia whole — 2 [hp_X]/1Aconitum napellus whole — 3 [hp_X]/1Matricaria chamomilla whole — 2 [hp_X]/1Achillea millefolium whole — 2 [hp_X]/1Atropa belladonna — 3 [hp_X]/1Hypericum perforatum whole — 3 [hp_X]/1Ruta graveolens flowering top — 4 [hp_X]/1Comfrey root — 8 [hp_X]/1
Dosage form: Tablet, Chewable
Route: Oral
Labeler: MediNatura Inc
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 20, 2023
Listing expires: Dec 31, 2026
Identifiers: Product ID 62795-2302_b8047305-bf5e-40a9-98b7-cc113890003bSPL ID b8047305-bf5e-40a9-98b7-cc113890003bSPL set ID 335c8bec-f0c3-4b95-a6a6-5fda262be0e6UNII O80TY208ZW, 18E7415PXQ, T7S323PKJS, 5EF0HWI5WU, 2HU33I03UY, VB06AV5US8, U0NQ8555JD, G0R4UBI2ZZ, 2FXJ6SW4PK, WQZ3G9PF0H, XK4IUX8MNB, N94C2U587S, M9VVZ08EKQUPC 0787647948406

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

N462795230202 followed by a unit qualifier and the quantity

Package 62795-2302-02. 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 20, 2023.

Indications (excerpt from the label)

Uses: For the temporary relief of minor symptoms of bruising and pain.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)