Guna-Fem NDC 17089-231

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-231Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0231Add 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
17089-231-18	17089023118	1 BOTTLE, DROPPER in 1 BOX (17089-231-18) / 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-Fem
Generic name (nonproprietary): adenosinum ciclophosphoricum - lilium tigrinum - melatonin - sus scrofa adrenal gland - sus scrofa corpus luteum - sus scrofa hypothalamus - sus scrofa ovary - sus scrofa pancreas - sus scrofa pineal gland - sus scrofa pituitary gland - sus scrofa thymus - thyroid -
Active ingredients: Adenosine cyclic phosphate — 6 [hp_X]/30mLSus scrofa corpus luteum — 30 [hp_X]/30mLSus scrofa adrenal gland — 30 [hp_X]/30mLSus scrofa pituitary gland — 30 [hp_X]/30mLSus scrofa hypothalamus — 30 [hp_X]/30mLLilium lancifolium bulb — 6 [hp_X]/30mLMelatonin — 200 [hp_X]/30mLSus scrofa ovary — 6 [hp_X]/30mLSus scrofa pancreas — 30 [hp_X]/30mLSus scrofa pineal gland — 30 [hp_X]/30mLSus scrofa thymus — 30 [hp_X]/30mLThyroid — 6 [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
Identifiers: Product ID 17089-231_53f5d23c-08d5-fd02-e063-6294a90a3cafSPL ID 53f5d23c-08d5-fd02-e063-6294a90a3cafSPL set ID 2a41728f-3270-42d7-aa4e-4c4572870d77UNII E0399OZS9N, 94X749MHSP, 398IYQ16YV, L0PFEMQ1DT, N6R0856Z79, 47Z05W73EZ, JL5DK93RCL, S7YTV04R8O, 9Y3J3362RY, 050QZ2EDK7, 7B69B0BD62, 6RV024OAUQUPC 0317089231189

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

N417089023118 followed by a unit qualifier and the quantity

Package 17089-0231-18. 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)