What is NDC 60986-2040?

60986-2040 is the product NDC for Ab, Aconitum napellus 3 [hp_X]/100mL; Bryonia cretica subsp. Dioica root 3 [hp_X]/100mL liquid, listed with the FDA by MARCO PHARMA INTERNATIONAL LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Ab (Aconitum napellus, Bryonia cretica).

What is the active ingredient?

Aconitum napellus, Bryonia cretica subsp. Dioica root.

MARCO PHARMA INTERNATIONAL LLC, NDC labeler code 60986. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Ab?

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.

Ab NDC 60986-2040 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)60986-2040Labeler and product segments. Claims need a package NDC.

Product NDC at billing width60986-2040Add 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
60986-2040-3	60986204003	50 mL in 1 BOTTLE (60986-2040-3)Marketed from Feb 6, 2025

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): Ab
Generic name (nonproprietary): aconitum napellus, bryonia cretica
Active ingredients: Aconitum napellus — 3 [hp_X]/100mLBryonia cretica subsp. Dioica root — 3 [hp_X]/100mL
Dosage form: Liquid
Route: Oral
Labeler: MARCO PHARMA INTERNATIONAL LLCNDC labeler code 60986
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 6, 2025
Listing expires: Dec 31, 2027
Identifiers: Product ID 60986-2040_483ad8b7-56c6-1dc3-e063-6394a90abb23SPL ID 483ad8b7-56c6-1dc3-e063-6394a90abb23SPL set ID 2d81c13f-102a-6741-e063-6294a90aee84UNII U0NQ8555JD, 53UB5FH7CX

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

N460986204003 followed by a unit qualifier and the quantity

Package 60986-2040-03. 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 Jan 12, 2026.

Indications (excerpt from the label)

FOR TEMPORARY RELIEF OF MINOR INFLAMMATION AND TRAUMA

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 60986-2040

What is NDC 60986-2040?: 60986-2040 is the product NDC for Ab, Aconitum napellus 3 [hp_X]/100mL; Bryonia cretica subsp. Dioica root 3 [hp_X]/100mL liquid, listed with the FDA by MARCO PHARMA INTERNATIONAL LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Ab (Aconitum napellus, Bryonia cretica).
What is the active ingredient?: Aconitum napellus, Bryonia cretica subsp. Dioica root.
Who is the labeler?: MARCO PHARMA INTERNATIONAL LLC, NDC labeler code 60986. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ab?: 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.

Ab (Aconitum napellus, bryonia cretica) NDC 60986-2040