Arnicare Arnica (arnica montana) NDC 0220-9059

NDC codes

FDA NDC Directory

Product NDC (as listed)0220-9059Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00220-9059Add 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
0220-9059-04	00220905904	60 TABLET in 1 BLISTER PACK (0220-9059-04)Marketed from Jul 11, 2011
0220-9059-29	00220905929	120 TABLET in 1 BLISTER PACK (0220-9059-29)Marketed from Apr 9, 2021
0220-9059-92	00220905992	100 TABLET in 1 BLISTER PACK (0220-9059-92)Marketed from Mar 20, 2025

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): Arnicare Arnica
Generic name (nonproprietary): arnica montana
Active ingredients: Arnica montana — 9 [hp_C]/1
Dosage form: Tablet
Route: Oral
Labeler: Laboratoires Boiron
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 11, 2011
Listing expires: Dec 31, 2026
Identifiers: Product ID 0220-9059_30d0f65b-a256-29b9-e063-6394a90a9b0fSPL ID 30d0f65b-a256-29b9-e063-6394a90a9b0fSPL set ID 96a3e7ea-94ed-46b4-94d7-70b8cc68c688UNII 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

N400220905904 followed by a unit qualifier and the quantity

Package 00220-9059-04. 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, 2025.

Indications (excerpt from the label)

Uses* temporarily relieves minor muscle pain and stiffness due to: minor injuries overexertion falls reduces symptoms of bruising such as: pain swelling discoloration

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)