Arnica Montana 30C HPUS (arnica montana) NDC 80004-300

NDC codes

FDA NDC Directory

Product NDC (as listed)80004-300Labeler and product segments. Claims need a package NDC.

Product NDC at billing width80004-0300Add 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
80004-300-10	80004030010	1 BOTTLE in 1 CARTON (80004-300-10) / 150 TABLET in 1 BOTTLEMarketed from Mar 14, 2022
80004-300-20	80004030020	1 BLISTER PACK in 1 CARTON (80004-300-20) / 30 TABLET in 1 BLISTER PACKMarketed from Mar 14, 2022

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 Montana 30C HPUSSuffix: 30C HPUS
Generic name (nonproprietary): arnica montana
Active ingredients: Arnica montana whole — 30 [hp_C]/1
Dosage form: Tablet
Route: Oral
Labeler: VITAMEDICA, INC.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 14, 2022
Listing expires: Dec 31, 2027
Identifiers: Product ID 80004-300_4e580e93-09b7-ad67-e063-6394a90aea01SPL ID 4e580e93-09b7-ad67-e063-6394a90aea01SPL set ID 3d6bfff9-16a2-8ff8-e063-6394a90a2bdaUNII 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

N480004030010 followed by a unit qualifier and the quantity

Package 80004-0300-10. 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 Mar 31, 2026.

Indications (excerpt from the label)

USES: *Temporarily relieves these symptoms: • Bruising • Swelling • Pain • Stiff • Muscle Soreness *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)