Guna Healthy Brain NDC 17089-500

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-500Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0500Add 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
17089-500-18	17089050018	1 BOTTLE, DROPPER in 1 BOX (17089-500-18) / 30 mL in 1 BOTTLE, DROPPERMarketed from Feb 17, 2021

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 Healthy Brain
Generic name (nonproprietary): citrullus colocynthis fruit pulp - ubidecarenone - sus scrifa adrenal gland - sus scrofa placenta - selenium - thuja occidentalis leafy twig - conium maculatum flowering top - sus scrofa embryo - aconitum napellus - aloe - barium oxalosuccinate - sus scrofa cerebrum - arnica montana - sus scrofa hypothalamus -
Active ingredients: Citrullus colocynthis fruit pulp — 4 [hp_X]/30mLSus scrofa embryo — 6 [hp_X]/30mLSus scrofa adrenal gland — 6 [hp_X]/30mLSus scrofa placenta — 6 [hp_X]/30mLSelenium — 6 [hp_X]/30mLThuja occidentalis leafy twig — 8 [hp_X]/30mLConium maculatum flowering top — 4 [hp_X]/30mLAconitum napellus — 4 [hp_X]/30mLAloe — 4 [hp_X]/30mLBarium oxalosuccinate — 6 [hp_X]/30mLSus scrofa cerebrum — 6 [hp_X]/30mLArnica montana — 3 [hp_X]/30mLSus scrofa hypothalamus — 6 [hp_X]/30mLUbidecarenone — 5 [hp_X]/30mL
Dosage form: Solution/ drops
Route: Oral
Labeler: Guna spa
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 17, 2021
Listing expires: Dec 31, 2026
Identifiers: Product ID 17089-500_ba48694e-5cb1-22ef-e053-2995a90a9965SPL ID ba48694e-5cb1-22ef-e053-2995a90a9965SPL set ID ba486fa9-53d1-95d9-e053-2995a90af42dUNII 23H32AOH17, 9928MC12VO, 398IYQ16YV, C8CV8867O8, H6241UJ22B, 1NT28V9397, Q28R5GF371, U0NQ8555JD, V5VD430YW9, L7A49804ZQ, 4GB5DQR532, O80TY208ZW, N6R0856Z79, EJ27X76M46UPC 0317089500186

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

N417089050018 followed by a unit qualifier and the quantity

Package 17089-0500-18. 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 Feb 17, 2021.

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)