Guna-Mood NDC 17089-265

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-265Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0265Add 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
17089-265-18	17089026518	1 BOTTLE, DROPPER in 1 BOX (17089-265-18) / 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-Mood
Generic name (nonproprietary): 5-hydroxy tryptophan,dl - alfalfa - avena sativa flowering top - lachesis muta venom - phosphoric acid - salix alba bark - salmonella enterica subsp. enterica serovar typhi - sepia officinalis juice - serotonin - strychnos ignatii seed - sus scrofa pineal gland - sus scrofa thymus - tryptophan -
Active ingredients: 5-hydroxytryptophan, Dl- — 3 [hp_X]/30mLAlfalfa — 6 [hp_X]/30mLAvena sativa flowering top — 6 [hp_X]/30mLStrychnos ignatii seed — 30 [hp_C]/30mLLachesis muta venom — 30 [hp_C]/30mLPhosphoric acid — 200 [hp_X]/30mLSus scrofa pineal gland — 200 [hp_X]/30mLSalix alba bark — 10 [hp_X]/30mLSalmonella enterica subsp. Enterica serovar typhi — 30 [hp_C]/30mLSepia officinalis juice — 30 [hp_C]/30mLSerotonin — 30 [hp_C]/30mLSus scrofa thymus — 200 [hp_X]/30mLTryptophan — 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: May 23, 2006
Listing expires: Dec 31, 2027
Identifiers: Product ID 17089-265_53e95b31-d0c4-682e-e063-6394a90a8f55SPL ID 53e95b31-d0c4-682e-e063-6394a90a8f55SPL set ID 3dc2b414-00b6-446c-a81e-3b023322a278UNII 9181P3OI6N, DJO934BRBD, MA9CQJ3F7F, 1NM3M2487K, VSW71SS07I, E4GA8884NN, 050QZ2EDK7, 205MXS71H7, 760T5R8B3O, QDL83WN8C2, 333DO1RDJY, 7B69B0BD62, 8DUH1N11BX

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

N417089026518 followed by a unit qualifier and the quantity

Package 17089-0265-18. 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 10, 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)