Fuligo NDC 85816-2060

NDC codes

FDA NDC Directory

Product NDC (as listed)85816-2060Labeler and product segments. Claims need a package NDC.

Product NDC at billing width85816-2060Add 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
85816-2060-1	85816206001	30 mL in 1 BOTTLE, GLASS (85816-2060-1)Marketed from Jan 1, 2015
85816-2060-2	85816206002	500 mL in 1 BOTTLE, GLASS (85816-2060-2)Marketed from Jan 1, 2015

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): Fuligo
Generic name (nonproprietary): cimicifuga, drosera, formica rufa, fuligo, inula hel., kali mur, lapis albus, silicea
Active ingredients: Black cohosh — 6 [hp_X]/mLDrosera rotundifolia whole — 6 [hp_X]/mLSilicon dioxide — 6 [hp_X]/mLCalcium hexafluorosilicate — 6 [hp_X]/mLInula helenium root — 6 [hp_X]/mLFormica rufa — 6 [hp_X]/mLPotassium chloride — 6 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BM Private Limited
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 1, 2015
Listing expires: Dec 31, 2027
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)
Identifiers: Product ID 85816-2060_4aa0ae4d-4592-8135-e063-6394a90a6a75SPL ID 4aa0ae4d-4592-8135-e063-6394a90a6a75SPL set ID 3b27225f-4587-d915-e063-6294a90a7225UNII K73E24S6X9, QR44N9XPJQ, ETJ7Z6XBU4, 2NVP93XVQ3, E55SMD6DA8, 55H0W83JO5, 660YQ98I10
Pharmacologic class: Osmotic Laxative; Potassium Salt

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

N485816206001 followed by a unit qualifier and the quantity

Package 85816-2060-01. 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 Feb 12, 2026.

Indications (excerpt from the label)

For detail, please read the enclosed package (product information leaflet)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)