What is NDC 68466-0004?

68466-0004 is the product NDC for Arniflora Gel (arnica montana), Arnica montana 1 [hp_X]/28g gel, listed with the FDA by Schwabe Mexico S.A. de C.V.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Arniflora Gel (Arnica montana).

Schwabe Mexico S.A. de C.V., NDC labeler code 68466. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Arniflora Gel?

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.

Arniflora Gel NDC 68466-0004 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68466-0004Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68466-0004Add 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
68466-0004-8	6846600040868466000408	1 TUBE in 1 CARTON (68466-0004-8) / 78 g in 1 TUBEMarketed from Jan 1, 2011

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): Arniflora Gel
Generic name (nonproprietary): arnica montana
Active ingredients: Arnica montana — 1 [hp_X]/28g
Dosage form: Gel
Route: Topical, Topical
Labeler: Schwabe Mexico S.A. de C.V.NDC labeler code 68466
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 1, 2011
Listing expires: Dec 31, 2026
Identifiers: Product ID 68466-0004_11f1a77b-71cd-41fb-945f-6d7d1d9b12e2SPL ID 11f1a77b-71cd-41fb-945f-6d7d1d9b12e2SPL set ID 2031b9b0-a188-43c9-95da-6488a3ba033dUNII O80TY208ZWUPC 0308078250977

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, Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N468466000408 followed by a unit qualifier and the quantity

Package 68466-0004-08. 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 Nov 21, 2025.

Indications (excerpt from the label)

Indications & Usage Temporarily relieves muscle pain, stiffness, and swelling associated with overexertion, sprains, falls, blows, and minor sports injuries. Reduces pain, swelling, and discoloration from bruises.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68466-0004

What is NDC 68466-0004?: 68466-0004 is the product NDC for Arniflora Gel (arnica montana), Arnica montana 1 [hp_X]/28g gel, listed with the FDA by Schwabe Mexico S.A. de C.V.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Arniflora Gel (Arnica montana).
What is the active ingredient?: Arnica montana.
Who is the labeler?: Schwabe Mexico S.A. de C.V., NDC labeler code 68466. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Arniflora Gel?: 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.

Arniflora Gel (Arnica montana) NDC 68466-0004