Aesculus NDC 60986-1027

NDC codes

FDA NDC Directory

Product NDC (as listed)60986-1027Labeler and product segments. Claims need a package NDC.

Product NDC at billing width60986-1027Add 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
60986-1027-3	60986102703	50 mL in 1 BOTTLE, GLASS (60986-1027-3)Marketed from Feb 27, 2018
60986-1027-4	60986102704	100 mL in 1 BOTTLE, GLASS (60986-1027-4)Marketed from Feb 27, 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): Aesculus
Generic name (nonproprietary): potentilla anserina, aesculus hippocastanum, ustilago maidis, secale cornutum, ruta graveolens
Active ingredients: Argentina anserina flowering top — 1 [hp_X]/mLHorse chestnut — 1 [hp_X]/mLUstilago maydis — 5 [hp_X]/mLClaviceps purpurea sclerotium — 4 [hp_X]/mLRuta graveolens whole — 3 [hp_X]/mL
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
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Fungal Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 60986-1027_483bfb8e-a23c-8c1c-e063-6294a90abcb1SPL ID 483bfb8e-a23c-8c1c-e063-6294a90abcb1SPL set ID 99365ce6-f7d1-483b-952b-2ef6a17d39abUNII H00Y243SK0, 3C18L6RJAZ, 4K7Z7K7SWG, 01G9XEA93N, 181JI0338P
Pharmacologic class: Non-Standardized Fungal Allergenic Extract

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

N460986102703 followed by a unit qualifier and the quantity

Package 60986-1027-03. 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 Adults: take 25 drops in tepid water three times daily. For severe symptoms take 20 drops five times daily until improvement is felt. Children receive 1/2 or less of the adult amount.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)