Guna-Diur NDC 17089-260

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-260Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0260Add 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
17089-260-18	17089026018	1 BOTTLE, DROPPER in 1 BOX (17089-260-18) / 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-Diur
Generic name (nonproprietary): amiloride - apis mellifera - berberis vulgaris fruit - hieracium pilosella flowering top - hydrochlorothiazide - solidago virgaurea flowering top - spironolactone - sus scrofa pituitary gland -
Active ingredients: Amiloride — 4 [hp_X]/30mLApis mellifera — 2 [hp_X]/30mLBerberis vulgaris fruit — .3 g/30mLHydrochlorothiazide — 4 [hp_X]/30mLSus scrofa pituitary gland — 12 [hp_X]/30mLHieracium pilosella flowering top — .3 g/30mLSolidago virgaurea flowering top — .3 g/30mLSpironolactone — 4 [hp_X]/30mL
Dosage form: Solution/ drops
Route: Oral
Labeler: Guna spa
Product type: Prescription drug
Marketing category: Unapproved homeopathic
Marketing start: May 23, 2006
Listing expires: Dec 31, 2026
Other FDA classes: Aldosterone Antagonists (Mechanism)Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Decreased Renal K+ Excretion (Physiologic effect)Increased Diuresis (Physiologic effect)Increased Diuresis (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Thiazides (Chemical structure)
Identifiers: Product ID 17089-260_7e7c2115-72fe-9ca5-e053-2a91aa0ae101SPL ID 7e7c2115-72fe-9ca5-e053-2a91aa0ae101SPL set ID 3f91cd92-eb6d-4bda-9cad-2e11e0b0fbe2UNII 7DZO8EB0Z3, 7S82P3R43Z, 6XEF22AHC3, 0J48LPH2TH, L0PFEMQ1DT, 08A7Y81S1P, 5405K23S50, 27O7W4T232
Pharmacologic class: Aldosterone Antagonist; Potassium-sparing Diuretic; Standardized Insect Venom Allergenic Extract; Thiazide Diuretic

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

N417089026018 followed by a unit qualifier and the quantity

Package 17089-0260-18. 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 Dec 21, 2018.

Indications (excerpt from the label)

1. INDICATIONS AND USAGE 1.1 Temporary relief of fluid retention 1.2 Tissue swelling and related disconforts

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)