What is NDC 60986-2025?

60986-2025 is the product NDC for Luffa, Luffa acutangula fruit 6 [hp_X]/1 + 7 more ingredients tablet, orally disintegrating, 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?

Luffa (Luffa, Hydrastis Canadensis, Mercurius Sulph. Rub, Allium Cepa, Natrum Muriticum, Phosphorus, Eupatorium Perf, Sticta).

What is the active ingredient?

Luffa acutangula fruit, Goldenseal, Mercuric sulfide, Onion, Sodium chloride, Phosphorus, Eupatorium perfoliatum flowering top, Lobaria pulmonaria.

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 Luffa?

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.

Luffa NDC 60986-2025 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)60986-2025Labeler and product segments. Claims need a package NDC.

Product NDC at billing width60986-2025Add 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
60986-2025-2	6098620250260986202502	60 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (60986-2025-2)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): Luffa
Generic name (nonproprietary): luffa, hydrastis canadensis, mercurius sulph. rub, allium cepa, natrum muriticum, phosphorus, eupatorium perf, sticta
Active ingredients: Luffa acutangula fruit — 6 [hp_X]/1Goldenseal — 4 [hp_X]/1Mercuric sulfide — 4 [hp_X]/1Onion — 6 [hp_X]/1Sodium chloride — 6 [hp_X]/1Phosphorus — 6 [hp_X]/1Eupatorium perfoliatum flowering top — 5 [hp_X]/1Lobaria pulmonaria — 2 [hp_X]/1
Dosage form: Tablet, Orally disintegrating
Route: Oral
Labeler: Marco Pharma International LLC.NDC labeler code 60986
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)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 60986-2025_483bedff-d761-3c5b-e063-6394a90a8eebSPL ID 483bedff-d761-3c5b-e063-6394a90a8eebSPL set ID 7dbb79de-c3f5-4245-884a-a6bd29bb861cUNII F0R3Y60C6V, ZW3Z11D0JV, ZI0T668SF1, 492225Q21H, 451W47IQ8X, 27YLU75U4W, 1W0775VX6E, D1YM0P5Z2T
Pharmacologic class: Non-Standardized Food Allergenic Extract; Osmotic Laxative

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

N460986202502 followed by a unit qualifier and the quantity

Package 60986-2025-02. 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)

Dosage Adults take 1 tablet three times daily, dissolving on the tongue. For severe symptoms, take 1 tablet every hour until improvement is felt. Children receive 1/2 or less the adult amount.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 60986-2025

What is NDC 60986-2025?: 60986-2025 is the product NDC for Luffa, Luffa acutangula fruit 6 [hp_X]/1 + 7 more ingredients tablet, orally disintegrating, 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?: Luffa (Luffa, Hydrastis Canadensis, Mercurius Sulph. Rub, Allium Cepa, Natrum Muriticum, Phosphorus, Eupatorium Perf, Sticta).
What is the active ingredient?: Luffa acutangula fruit, Goldenseal, Mercuric sulfide, Onion, Sodium chloride, Phosphorus, Eupatorium perfoliatum flowering top, Lobaria pulmonaria.
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 Luffa?: 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.