What is NDC 60986-2020?

60986-2020 is the product NDC for Echinacea, Echinacea angustifolia 1 [hp_X]/1 + 10 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?

Echinacea (Echinacea angustifolia, Hamammelis virginiana, Calcarea phosphorica, Hydrastis canadanesis, Senega officinalis, Silicea, Conium, Aurum muriaticum natronatum, Calcarea carbonica, Fucus vesiculosus, Lachesis mutus).

What is the active ingredient?

Echinacea angustifolia, Hamamelis virginiana root bark/stem bark, Tribasic calcium phosphate, Goldenseal, Polygala senega root, Silicon dioxide, Conium maculatum flowering top, Sodium tetrachloroaurate, Oyster shell calcium carbonate, Crude, Fucus vesiculosus, Lachesis muta venom.

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 Echinacea?

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.

Echinacea NDC 60986-2020 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)60986-2020Labeler and product segments. Claims need a package NDC.

Product NDC at billing width60986-2020Add 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
60986-2020-2	6098620200260986202002	100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (60986-2020-2)Marketed from Mar 26, 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): Echinacea
Generic name (nonproprietary): echinacea angustifolia, hamammelis virginiana, calcarea phosphorica, hydrastis canadanesis, senega officinalis, silicea, conium, aurum muriaticum natronatum, calcarea carbonica, fucus vesiculosus, lachesis mutus
Active ingredients: Echinacea angustifolia — 1 [hp_X]/1Hamamelis virginiana root bark/stem bark — 2 [hp_X]/1Tribasic calcium phosphate — 3 [hp_X]/1Goldenseal — 4 [hp_X]/1Polygala senega root — 4 [hp_X]/1Silicon dioxide — 4 [hp_X]/1Conium maculatum flowering top — 4 [hp_X]/1Sodium tetrachloroaurate — 5 [hp_X]/1Oyster shell calcium carbonate, Crude — 5 [hp_X]/1Fucus vesiculosus — 5 [hp_X]/1Lachesis muta venom — 8 [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: Calcium (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Phosphate Chelating Activity (Mechanism)
Identifiers: Product ID 60986-2020_483b5b77-9991-87fa-e063-6394a90a6c1eSPL ID 483b5b77-9991-87fa-e063-6394a90a6c1eSPL set ID 7efadb70-99e4-428b-a8ef-a2797327c6faUNII VB06AV5US8, T7S323PKJS, 91D9GV0Z28, ZW3Z11D0JV, M7T6H7D4IF, ETJ7Z6XBU4, Q28R5GF371, 7FT6QUT299, 2E32821G6I, 535G2ABX9M, VSW71SS07I
Pharmacologic class: Blood Coagulation Factor; Phosphate Binder

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

N460986202002 followed by a unit qualifier and the quantity

Package 60986-2020-02. 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 one tablet every hour until improvement is felt. Children receive 1/2 tablet as above.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 60986-2020

What is NDC 60986-2020?: 60986-2020 is the product NDC for Echinacea, Echinacea angustifolia 1 [hp_X]/1 + 10 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?: Echinacea (Echinacea angustifolia, Hamammelis virginiana, Calcarea phosphorica, Hydrastis canadanesis, Senega officinalis, Silicea, Conium, Aurum muriaticum natronatum, Calcarea carbonica, Fucus vesiculosus, Lachesis mutus).
What is the active ingredient?: Echinacea angustifolia, Hamamelis virginiana root bark/stem bark, Tribasic calcium phosphate, Goldenseal, Polygala senega root, Silicon dioxide, Conium maculatum flowering top, Sodium tetrachloroaurate, Oyster shell calcium carbonate, Crude, Fucus vesiculosus, Lachesis muta venom.
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 Echinacea?: 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.