Guna-Awareness NDC 17089-350

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-350Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0350Add 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
17089-350-18	17089035018	1 BOTTLE, DROPPER in 1 BOX (17089-350-18) / 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-Awareness
Generic name (nonproprietary): betaine - bufo bufo cutaneous gland - calcium carbonate - chromic sulfate - cicuta virosa root - copper - folic acid - gold - cobalamin - iron - lachesis muta venom - melatonin - molybdenum - neurotrophin-3 - neurotrophin-4 - oxytocin - silicon dioxide - sus scrofa frontal lobe - sus scrofa temporal lobe - thyrotropin alfa - ubidecarenone - vanadium - zinc - brain-derived neurotrophic factor human -
Active ingredients: Lachesis muta venom — 12 [hp_X]/30mLMelatonin — 4 [hp_C]/30mLMolybdenum — 3 [hp_X]/30mLNeurotrophin-3 — 4 [hp_C]/30mLNeurotrophin-4 — 4 [hp_C]/30mLOxytocin — 6 [hp_X]/30mLSilicon dioxide — 12 [hp_X]/30mLSus scrofa temporal lobe — 6 [hp_X]/30mLThyrotropin alfa — 3 [hp_X]/30mLBetaine — 3 [hp_X]/30mLVanadium — 6 [hp_X]/30mLZinc — 3 [hp_X]/30mLGold — 12 [hp_X]/30mLBrain-derived neurotrophic factor human — 4 [hp_C]/30mLBufo bufo cutaneous gland — 12 [hp_X]/30mLCalcium carbonate — 3 [hp_X]/30mLChromic sulfate — 3 [hp_X]/30mLCicuta virosa root — 12 [hp_X]/30mLCobalamin — 3 [hp_X]/30mLUbidecarenone — 3 [hp_X]/30mLCopper — 12 [hp_X]/30mLIron — 3 [hp_X]/30mLFolic acid — 3 [hp_X]/30mLSus scrofa frontal lobe — 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: Apr 16, 2008
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Calcium (Chemical structure)Divalent (Chemical structure)Cell-mediated Immunity (Physiologic effect)Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Increased Coagulation Factor Activity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Uterine Smooth Muscle Contraction or Tone (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)Methylating Activity (Mechanism)Oxytocin (Chemical structure)Phosphate Chelating Activity (Mechanism)Thyrotropin (Chemical structure)
Identifiers: Product ID 17089-350_53e9c346-d910-c7fb-e063-6294a90a0a3eSPL ID 53e9c346-d910-c7fb-e063-6294a90a0a3eSPL set ID 10e46b39-7903-4390-b72d-865291245b4cUNII VSW71SS07I, JL5DK93RCL, 81AH48963U, 02R4V6T25Y, P658DCA9XD, 1JQS135EYN, ETJ7Z6XBU4, 490XI1KB4S, AVX3D5A4LM, 3SCV180C9W, 00J9J9XKDE, J41CSQ7QDS, 79Y1949PYO, A1ED6W905I, Q59QU6N72Q, H0G9379FGK, Y0C99N5TMZ, YEA9P21S8N, 8406EY2OQA, EJ27X76M46, 789U1901C5, E1UOL152H7, 935E97BOY8, GV54Q19G55UPC 0317089350187
Pharmacologic class: Blood Coagulation Factor; Copper-containing Intrauterine Device; Methylating Agent; Oxytocic; Phosphate Binder; Standardized Chemical Allergen; Thyroid Stimulating Hormone

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

N417089035018 followed by a unit qualifier and the quantity

Package 17089-0350-18. 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)