Traulevium NDC 70857-002

NDC codes

FDA NDC Directory

Product NDC (as listed)70857-002Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70857-0002Add 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
70857-002-10	70857000210	100 TABLET, CHEWABLE in 1 BOTTLE (70857-002-10)Marketed from Oct 3, 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): belladonna, arnica montana radix, aconitum napellus, chamomilla, symphytum officinale, calendula officinalis, hamamelis virginiana, millefolium, hepar sulphuris calcareum, mercurius solubilis, hypericum perforatum, bellis perennis, echinacea angustifolia, echinacea purpurea.
Active ingredients: Atropa belladonna — 4 [hp_X]/1Arnica montana — 3 [hp_X]/1Aconitum napellus — 3 [hp_X]/1Matricaria recutita — 3 [hp_X]/1Comfrey root — 8 [hp_X]/1Calendula officinalis flowering top — 2 [hp_X]/1Hamamelis virginiana root bark/stem bark — 2 [hp_X]/1Achillea millefolium — 3 [hp_X]/1Calcium sulfide — 8 [hp_X]/1Mercurius solubilis — 8 [hp_X]/1Hypericum perforatum — 3 [hp_X]/1Bellis perennis — 2 [hp_X]/1Echinacea angustifolia — 2 [hp_X]/1Echinacea purpurea — 2 [hp_X]/1
Dosage form: Tablet, Chewable
Route: Oral
Labeler: Medical Technology Products, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 3, 2016
Listing expires: Dec 31, 2026
Identifiers: Product ID 70857-002_d44bff7e-57cc-a6fa-e053-2a95a90a4e04SPL ID d44bff7e-57cc-a6fa-e053-2a95a90a4e04SPL set ID 6123d145-4edf-4ecd-8b30-196e52273127UNII WQZ3G9PF0H, O80TY208ZW, U0NQ8555JD, G0R4UBI2ZZ, M9VVZ08EKQ, 18E7415PXQ, T7S323PKJS, 2FXJ6SW4PK, 1MBW07J51Q, 324Y4038G2, XK4IUX8MNB, 2HU33I03UY, VB06AV5US8, QI7G114Y98UPC 0742574246544

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

N470857000210 followed by a unit qualifier and the quantity

Package 70857-0002-10. 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** 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)