Traulevium NDC 70857-001

NDC codes

FDA NDC Directory

Product NDC (as listed)70857-001Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70857-0001Add 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
70857-001-50	70857000150	1 TUBE in 1 BOX (70857-001-50) / 50 g in 1 TUBEMarketed from Oct 12, 2016

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Traulevium
Generic name (nonproprietary): arnica montana radix, calendula officinalis, hamamelis virginiana, echinacea, echinacea purpurea, chamomilla, symphytum officinale, bellis perennis, hypericum perforatum, millefolium, aconitum napellus, belladonna, mercurius solubilis, hepar sulphuris calcareum.
Active ingredients: Arnica montana root — 3 [hp_X]/50gCalendula officinalis flowering top — 225 mg/50gHamamelis virginiana root bark/stem bark — 225 mg/50gEchinacea, Unspecified — 75 mg/50gEchinacea purpurea — 75 mg/50gMatricaria recutita — 75 mg/50gComfrey root — 6 [hp_X]/50gBellis perennis — 50 mg/50gHypericum perforatum — 6 [hp_X]/50gAchillea millefolium — 45 mg/50gAconitum napellus — 4 [hp_X]/50gAtropa belladonna — 1 [hp_X]/50gMercurius solubilis — 6 [hp_X]/50gCalcium sulfide — 6 [hp_X]/50g
Dosage form: Ointment
Route: Topical
Labeler: Medical Technology Products, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 12, 2016
Listing expires: Dec 31, 2026
Identifiers: Product ID 70857-001_d44c2b78-496a-70f3-e053-2a95a90a9ffdSPL ID d44c2b78-496a-70f3-e053-2a95a90a9ffdSPL set ID 797f448f-a4c7-4c7a-980d-7c3b074e6499UNII MUE8Y11327, 18E7415PXQ, T7S323PKJS, 4N9P6CC1DX, QI7G114Y98, G0R4UBI2ZZ, M9VVZ08EKQ, 2HU33I03UY, XK4IUX8MNB, 2FXJ6SW4PK, U0NQ8555JD, WQZ3G9PF0H, 324Y4038G2, 1MBW07J51Q

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

N470857000150 followed by a unit qualifier and the quantity

Package 70857-0001-50. 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 Dec 29, 2021.

Indications (excerpt from the label)

USES Uses** For the temporary relief of: Joint Pain Back Pain Muscular Pain

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)