Arnica Cream (arnica montana) NDC 62106-1180

NDC codes

FDA NDC Directory

Product NDC (as listed)62106-1180Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62106-1180Add 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
62106-1180-0	62106118000	1 TUBE in 1 CARTON (62106-1180-0) / 40 g in 1 TUBEMarketed from Jan 20, 2015

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 Cream
Generic name (nonproprietary): arnica montana
Active ingredients: Arnica montana — 1 [hp_X]/40gCalendula officinalis flowering top — 1 [hp_X]/40g
Dosage form: Cream
Route: Topical
Labeler: Seroyal USA
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 20, 2015
Listing expires: Dec 31, 2026
Identifiers: Product ID 62106-1180_dc794e74-8ef3-7942-e053-2a95a90a2beaSPL ID dc794e74-8ef3-7942-e053-2a95a90a2beaSPL set ID 079c4f1c-836d-1113-e054-00144ff8d46cUNII O80TY208ZW, 18E7415PXQUPC 0883196316403, 0883196316304

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

N462106118000 followed by a unit qualifier and the quantity

Package 62106-1180-00. 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 Apr 12, 2022.

Indications (excerpt from the label)

Uses For the temporary relief of symptoms associated with minor cuts and burns Directions Adults: Apply a small amount on the affected area two to three times daily, or as recommended by your healthcare practitioner. Children: Use under the direction of your healthcare practitioner.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)