Guna-Kidney NDC 17089-298

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-298Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0298Add 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
17089-298-18	17089029818	1 BOTTLE, DROPPER in 1 BOX (17089-298-18) / 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-Kidney
Generic name (nonproprietary): chondrodendron tomentosum root - clerodendranthus spicatus leaf - equisetum hyemale - escherichia coli - hieracium pilosella flowering top - methylene blue - nitric acid - ononis campestris - plantago major - pork kidney - potassium nitrate - proteus vulgaris - quinhydrone - sarsaparilla - solidago virgaurea flowering top - succinic acid - sus scrofa ureter - sus scrofa urinary bladder -
Active ingredients: Escherichia coli — 12 [hp_X]/30mLEquisetum hyemale — 3 [hp_X]/30mLPotassium nitrate — 12 [hp_X]/30mLPork kidney — 8 [hp_X]/30mLMethylene blue — 8 [hp_X]/30mLHieracium pilosella flowering top — 1 [hp_X]/30mLNitric acid — 12 [hp_X]/30mLOnonis campestris — 2 [hp_X]/30mLClerodendranthus spicatus leaf — 2 [hp_X]/30mLChondrodendron tomentosum root — 2 [hp_X]/30mLPlantago major — 2 [hp_X]/30mLProteus vulgaris — 12 [hp_X]/30mLQuinhydrone — 8 [hp_X]/30mLSarsaparilla — 2 [hp_X]/30mLSolidago virgaurea flowering top — 1 [hp_X]/30mLSuccinic acid — 6 [hp_X]/30mLSus scrofa ureter — 8 [hp_X]/30mLSus scrofa urinary bladder — 8 [hp_X]/30mL
Dosage form: Solution/ drops
Route: Oral
Labeler: Guna spa
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 23, 2006
Listing expires: Dec 31, 2027
Other FDA classes: Depigmenting Activity (Physiologic effect)Melanin Synthesis Inhibitors (Mechanism)Oxidation-Reduction Activity (Mechanism)
Identifiers: Product ID 17089-298_53f52cf0-04e8-1d34-e063-6394a90a3bdcSPL ID 53f52cf0-04e8-1d34-e063-6394a90a3bdcSPL set ID 45c3c1af-e2b4-4239-98d9-f675c0e7d322UNII 514B9K0L10, 59677RXH25, RU45X2JN0Z, X7BCI5P86H, T42P99266K, 08A7Y81S1P, 411VRN1TV4, RP8496915M, DSS8V86H3Y, 395A3P448Z, W2469WNO6U, 11T9HCO30O, P4A66LQ3QJ, 2H1576D5WG, 5405K23S50, AB6MNQ6J6L, 7PGE2DJ8QM, 3G7U72W8DA
Pharmacologic class: Melanin Synthesis Inhibitor; Oxidation-Reduction Agent

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

N417089029818 followed by a unit qualifier and the quantity

Package 17089-0298-18. 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)