Sabal Serrulatum NDC 60986-1009

NDC codes

FDA NDC Directory

Product NDC (as listed)60986-1009Labeler and product segments. Claims need a package NDC.

Product NDC at billing width60986-1009Add 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
60986-1009-3	60986100903	50 mL in 1 BOTTLE, GLASS (60986-1009-3)Marketed from Feb 28, 2018
60986-1009-4	60986100904	100 mL in 1 BOTTLE, GLASS (60986-1009-4)Marketed from Feb 28, 2018

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): Sabal Serrulatum
Generic name (nonproprietary): sabal serulatum, lycopodium clavatum, pareira brava
Active ingredients: Saw palmetto — 1 [hp_X]/100mLLycopodium clavatum spore — 4 [hp_X]/100mLChondrodendron tomentosum root — 4 [hp_X]/100mL
Dosage form: Liquid
Route: Oral
Labeler: Marco Pharma International LLC.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 1, 1992
Listing expires: Dec 31, 2027
Identifiers: Product ID 60986-1009_483c0b7f-aa46-c983-e063-6294a90a16c2SPL ID 483c0b7f-aa46-c983-e063-6294a90a16c2SPL set ID 158394db-fc09-4a17-a55b-12329d972c2aUNII J7WWH9M8QS, C88X29Y479, 395A3P448Z

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

N460986100903 followed by a unit qualifier and the quantity

Package 60986-1009-03. 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)

Suggested use In acute disorders, take 10 drops in pure water every hour until improvement is felt. Then take 25 drops in pure water three times daily after or between meals.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)