Guna-Virus NDC 17089-503

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-503Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0503Add 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
17089-503-20	17089050320	2 TUBE in 1 BOX (17089-503-20) / 4 g in 1 TUBEMarketed from Jul 1, 2026

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-Virus
Generic name (nonproprietary): aldesleukin - everlasting extract - fomitopsis pinicola fruiting body - interferon gamma-1b - melatonin - metenkefalin - reishi - serotonin - soybean - sus scrofa blood - sus scrofa small intestine mucosa lymph follicle - sus scrofa spleen -
Active ingredients: Aldesleukin — 5 [hp_C]/4gEverlasting extract — 3 [hp_X]/4gFomitopsis pinicola fruiting body — 8 [hp_X]/4gInterferon gamma-1b — 3 [hp_C]/4gMetenkefalin — 4 [hp_C]/4gReishi — 8 [hp_X]/4gSerotonin — 6 [hp_X]/4gSoybean — 3 [hp_X]/4gSus scrofa blood — 4 [hp_C]/4gSus scrofa spleen — 4 [hp_C]/4gMelatonin — 15 [hp_C]/4gSus scrofa small intestine mucosa lymph follicle — 7 [hp_C]/4g
Dosage form: Pellet
Route: Oral
Labeler: Guna spa
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 1, 2006
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 Lymphocyte Activation (Physiologic effect)Increased Lymphocyte Cell Production (Physiologic effect)Interferon-gamma (Chemical structure)Interleukin-2 (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 17089-503_53e75d71-d919-2bc0-e063-6294a90a1d7fSPL ID 53e75d71-d919-2bc0-e063-6294a90a1d7fSPL set ID 53e741c4-8897-71f3-e063-6394a90a751dUNII M89N0Q7EQR, KQV867ADR4, 30D02U2IRN, 21K6M2I7AG, 9JEZ9OD3AS, TKD8LH0X2Z, 333DO1RDJY, L7HT8F1ZOD, 994R458ECK, 92AMN5J79Y, JL5DK93RCL, 308LM01C72
Pharmacologic class: Interferon gamma; Lymphocyte Growth Factor; Non-Standardized Food 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

N417089050320 followed by a unit qualifier and the quantity

Package 17089-0503-20. 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 Jul 1, 2026.

Indications (excerpt from the label)

DIRECTIONS Turn tube upside down and rotate cap to release pellets into cap. Unscrew cap and without touching pellets tip them into the mouth under the tongue. Allow to dissolve Take 15 minutes before meals.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)