Guna-Prostate NDC 17089-346

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-346Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0346Add 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
17089-346-18	17089034618	1 BOTTLE, DROPPER in 1 BOX (17089-346-18) / 30 mL in 1 BOTTLE, DROPPERMarketed from Dec 21, 2018

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-Prostate
Generic name (nonproprietary): aldesleukin - barium carbonate - chaste tree - chimaphila umbellata - clematis vitalba - conium maculatum flowering top - delphinium staphisagria seed - digitalis - ferric picrate - human interleukin-10 (nonglycosylated) - interferon gamma-1b - melatonin - saw palmetto - selenium - sus scrofa prostate - thuja occidentalis twig - transforming growth factor beta-1 - zinc -
Active ingredients: Ferric picrate — 30 [hp_X]/30mLChaste tree — 6 [hp_X]/30mLBarium carbonate — 30 [hp_X]/30mLChimaphila umbellata — 6 [hp_X]/30mLClematis recta flowering top — 3 [hp_X]/30mLConium maculatum flowering top — 30 [hp_X]/30mLDigitalis — 30 [hp_X]/30mLInterferon gamma-1b — 4 [hp_C]/30mLInterleukin-10 — 4 [hp_C]/30mLAldesleukin — 4 [hp_C]/30mLMelatonin — 4 [hp_C]/30mLSus scrofa prostate — 200 [hp_X]/30mLSaw palmetto — 3 [hp_X]/30mLSelenium — 30 [hp_X]/30mLDelphinium staphisagria seed — 30 [hp_X]/30mLTransforming growth factor beta-1 — 4 [hp_C]/30mLThuja occidentalis leafy twig — 30 [hp_X]/30mLZinc — 3 [hp_X]/30mL
Dosage form: Solution/ drops
Route: Oral
Labeler: Guna spa
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 1, 2017
Listing expires: Dec 31, 2027
Other FDA classes: Increased Lymphocyte Activation (Physiologic effect)Increased Lymphocyte Cell Production (Physiologic effect)Interferon-gamma (Chemical structure)Interleukin-2 (Chemical structure)Iron (Chemical structure)Phosphate Chelating Activity (Mechanism)
Identifiers: Product ID 17089-346_53f5c4b3-0eb0-5d70-e063-6394a90aa779SPL ID 53f5c4b3-0eb0-5d70-e063-6394a90aa779SPL set ID b99bb9ea-339c-4476-8e3c-e1fcbcfd5cdaUNII KZM8ZRY36A, 433OSF3U8A, 6P669D8HQ8, WCK21A9W9J, 396421SP9F, Q28R5GF371, F1T8QT9U8B, 21K6M2I7AG, 9SC4O216V9, M89N0Q7EQR, JL5DK93RCL, O6UD3347K2, J7WWH9M8QS, H6241UJ22B, 00543AP1JV, T7D25J14LT, 1NT28V9397, J41CSQ7QDSUPC 0317089346180
Pharmacologic class: Interferon gamma; Lymphocyte Growth Factor; Parenteral Iron Replacement; 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

N417089034618 followed by a unit qualifier and the quantity

Package 17089-0346-18. 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 Jun 11, 2026.

Indications (excerpt from the label)

Take 15 minutes before meals.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)