Guna-Flu NDC 17089-025

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-025Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0025Add 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
17089-025-17	17089002517	6 TUBE in 1 BOX (17089-025-17) / 1 g in 1 TUBEMarketed from May 23, 2006

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Guna-Flu
Generic name (nonproprietary): aconitum napellus - asclepias curassavica - atropa belladonna - cairina moschata heart/liver autolysate - copper - echinacea angustifolia - haemophilus influenzae type b -
Active ingredients: Aconitum napellus — 5 [hp_C]/gCairina moschata heart/liver autolysate — 7 [hp_C]/gAsclepias curassavica — 5 [hp_C]/gAtropa belladonna — 5 [hp_C]/gCopper — 3 [hp_C]/gEchinacea angustifolia — 3 [hp_C]/gHaemophilus influenzae type b — 9 [hp_C]/g
Dosage form: Pellet
Route: Oral
Labeler: Guna spa
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 23, 2006
Listing expires: Dec 31, 2026
Other FDA classes: Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)
Identifiers: Product ID 17089-025_92ac92a1-762e-5c83-e053-2995a90a3350SPL ID 92ac92a1-762e-5c83-e053-2995a90a3350SPL set ID 84e8e18c-8a74-41d5-b285-1ecb788bba3dUNII U0NQ8555JD, RN2HC612GY, JSZ93E47EP, WQZ3G9PF0H, 789U1901C5, VB06AV5US8, F2TW0N64FI
Pharmacologic class: Copper-containing Intrauterine Device

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

N417089002517 followed by a unit qualifier and the quantity

Package 17089-0025-17. 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 Nov 14, 2022.

Indications (excerpt from the label)

Directions : pour the content of 1 tube directly into the mouth and allow to dissolve under the tongue. Take on an empty stomach.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)