What is NDC 53645-1004?

53645-1004 is the product NDC for Arnica 6X, Arnica montana root 6 [hp_X]/30mL; Arnica montana flower 6 [hp_X]/30mL liquid, listed with the FDA by True Botanica, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What is the active ingredient?

Arnica montana root, Arnica montana flower.

True Botanica, LLC, NDC labeler code 53645. 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 6X?

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 6X NDC 53645-1004 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)53645-1004Labeler and product segments. Claims need a package NDC.

Product NDC at billing width53645-1004Add 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
53645-1004-6	53645100406	30 mL in 1 BOTTLE (53645-1004-6)Marketed from Aug 1, 2024

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 6X
Generic name (nonproprietary): arnica 6x
Active ingredients: Arnica montana root — 6 [hp_X]/30mLArnica montana flower — 6 [hp_X]/30mL
Dosage form: Liquid
Route: Oral
Labeler: True Botanica, LLCNDC labeler code 53645
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 1, 2024
Listing expires: Dec 31, 2026
Identifiers: Product ID 53645-1004_1d5ff5bb-47b7-ebd1-e063-6394a90a84c9SPL ID 1d5ff5bb-47b7-ebd1-e063-6394a90a84c9SPL set ID 1d5fd20f-00dc-c8fe-e063-6394a90afae7UNII MUE8Y11327, OZ0E5Y15PZ

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

N453645100406 followed by a unit qualifier and the quantity

Package 53645-1004-06. 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 Aug 1, 2024.

Indications (excerpt from the label)

Use: For temporary relief of minor trauma and shocks. May also be used for standard homeopathic indications or as directed by your physician.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 53645-1004

What is NDC 53645-1004?: 53645-1004 is the product NDC for Arnica 6X, Arnica montana root 6 [hp_X]/30mL; Arnica montana flower 6 [hp_X]/30mL liquid, listed with the FDA by True Botanica, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Arnica 6X.
What is the active ingredient?: Arnica montana root, Arnica montana flower.
Who is the labeler?: True Botanica, LLC, NDC labeler code 53645. 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 6X?: 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.