Arnica Recovery (arnica montana) NDC 34666-010

NDC codes

FDA NDC Directory

Product NDC (as listed)34666-010Labeler and product segments. Claims need a package NDC.

Product NDC at billing width34666-0010Add 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
34666-010-12	34666001012	12 TABLET in 1 BLISTER PACK (34666-010-12)Marketed from Mar 1, 2018
34666-010-60	34666001060	60 TABLET in 1 BLISTER PACK (34666-010-60)Marketed from Jul 1, 2011

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): Arnica Recovery
Generic name (nonproprietary): arnica montana
Active ingredients: Arnica montana — 6 [hp_C]/1
Dosage form: Tablet
Route: Oral
Labeler: NARTEX LABORATORIOS HOMEOPATICOS SA DE CV
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 1, 2011
Listing expires: Dec 31, 2026
Identifiers: Product ID 34666-010_6637cdc3-5654-4469-e053-2991aa0abb48SPL ID 6637cdc3-5654-4469-e053-2991aa0abb48SPL set ID e9e22991-48a0-4e66-bd6f-267f3e8badd6UNII O80TY208ZW

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

N434666001012 followed by a unit qualifier and the quantity

Package 34666-0010-12. 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 Feb 27, 2018.

Indications (excerpt from the label)

For the temporary relief of sore muscles bruises sprains as per homeopathic materia medica Product uses are based on Homeopathic Materia Medica. These "Uses" have not been evaluated by teh Food and Drug Administration. This product has not been clinically tested by Nartex Labs USA, Inc.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)