Arnicare (arnica montana) NDC 0220-9021

NDC codes

FDA NDC Directory

Product NDC (as listed)0220-9021Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00220-9021Add 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
0220-9021-60	00220902160	40 g in 1 TUBE (0220-9021-60)Marketed from Mar 1, 2007
0220-9021-63	00220902163	70 g in 1 TUBE (0220-9021-63)Marketed from Mar 1, 2007
0220-9021-68	00220902168	1 TUBE in 1 BOX (0220-9021-68) / 14 g in 1 TUBEMarketed from Feb 29, 2016
0220-9021-82	00220902182	1 TUBE in 1 BOX (0220-9021-82) / 120 g in 1 TUBEMarketed from Jun 1, 2018
0220-9021-88	00220902188	2 TUBE in 1 BOX (0220-9021-88) / 120 g in 1 TUBEMarketed from Jul 21, 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
Generic name (nonproprietary): arnica montana
Active ingredients: Arnica montana — 1 [hp_X]/g
Dosage form: Cream
Route: Topical
Labeler: Laboratoires Boiron
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 1, 2007
Listing expires: Dec 31, 2027
Identifiers: Product ID 0220-9021_5242ebff-163f-ebd4-e063-6294a90a61dfSPL ID 5242ebff-163f-ebd4-e063-6294a90a61dfSPL set ID 542b41dd-f285-4e48-a67b-8e69523b143aUNII O80TY208ZWUPC 0306962032555

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

N400220902160 followed by a unit qualifier and the quantity

Package 00220-9021-60. 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 May 20, 2026.

Indications (excerpt from the label)

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)