What is NDC 61096-1032?

61096-1032 is the product NDC for Arnica Power (arnica montana), Arnica montana whole 3 [hp_X]/41mL liquid, listed with the FDA by Eight and Company L.L.C. It has 1 package NDC, shown above in 10- and 11-digit form.

Eight and Company L.L.C, NDC labeler code 61096. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Arnica Power?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Arnica Power NDC 61096-1032 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)61096-1032Labeler and product segments. Claims need a package NDC.

Product NDC at billing width61096-1032Add 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
61096-1032-1	61096103201	1 BOTTLE, SPRAY in 1 CARTON (61096-1032-1) / 41 mL in 1 BOTTLE, SPRAYMarketed from Mar 8, 2019

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 Power
Generic name (nonproprietary): arnica montana
Active ingredients: Arnica montana whole — 3 [hp_X]/41mL
Dosage form: Liquid
Route: Oral
Labeler: Eight and Company L.L.CNDC labeler code 61096
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 8, 2019
Listing expires: Dec 31, 2026
Identifiers: Product ID 61096-1032_1c3e7699-74cd-441a-92f3-d27b8267e8d9SPL ID 1c3e7699-74cd-441a-92f3-d27b8267e8d9SPL set ID 48c84c56-1179-4be5-84aa-033ddcb8e80cUNII O80TY208ZWUPC 0361096003215

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

N461096103201 followed by a unit qualifier and the quantity

Package 61096-1032-01. 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 Dec 18, 2025.

Indications (excerpt from the label)

INDICATIONS: Temporarily relieves symptoms associated with overexertion or trauma, such as: muscle aches stiffness swelling from injuries bruising ° natural ° gluten & lactose free ° no artificial flavors or colors ° vegan ° no known negative side effects ° no known negative drug interactions

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 61096-1032

What is NDC 61096-1032?: 61096-1032 is the product NDC for Arnica Power (arnica montana), Arnica montana whole 3 [hp_X]/41mL liquid, listed with the FDA by Eight and Company L.L.C. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Arnica Power (Arnica montana).
What is the active ingredient?: Arnica montana whole.
Who is the labeler?: Eight and Company L.L.C, NDC labeler code 61096. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Arnica Power?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Arnica Power (Arnica montana) NDC 61096-1032