Guna-Dizzy NDC 17089-306

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-306Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0306Add 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
17089-306-18	17089030618	1 BOTTLE, DROPPER in 1 BOX (17089-306-18) / 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-Dizzy
Generic name (nonproprietary): .alpha.-ketoglutaric acid - ambergris - anamirta cocculus seed - conium maculatum flowering top - epinephrine - fumaric acid - malic acid - melatonin - mineral oil - pteridium aquilinum root - pyridoxine hydrochloride - quinhydrone - quinine - sus scrofa artery - sus scrofa cerebellum - sus scrofa placenta - thiamine hydrochloride - tobacco leaf -
Active ingredients: Epinephrine — 6 [hp_X]/30mL.alpha.-ketoglutaric acid — 6 [hp_X]/30mLAmbergris — 6 [hp_X]/30mLSus scrofa artery — 6 [hp_X]/30mLSus scrofa cerebellum — 6 [hp_X]/30mLQuinine salicylate — 6 [hp_X]/30mLAnamirta cocculus seed — 4 [hp_X]/30mLConium maculatum flowering top — 3 [hp_X]/30mLFumaric acid — 6 [hp_X]/30mLMalic acid — 6 [hp_X]/30mLMelatonin — 4 [hp_C]/30mLMineral oil — 8 [hp_X]/30mLSus scrofa placenta — 6 [hp_X]/30mLPteridium aquilinum root — 8 [hp_X]/30mLPyridoxine hydrochloride — 6 [hp_X]/30mLQuinhydrone — 6 [hp_X]/30mLTobacco leaf — 6 [hp_X]/30mLThiamine hydrochloride — 4 [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, 2026
Other FDA classes: Adrenergic alpha-Agonists (Mechanism)Adrenergic beta-Agonists (Mechanism)Allergens (Chemical structure)Analogs/Derivatives (Chemical/Ingredient)Catecholamines (Chemical structure)Cell-mediated Immunity (Physiologic effect)Depigmenting Activity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Melanin Synthesis Inhibitors (Mechanism)Plant Proteins (Chemical structure)Vitamin B 6 (Chemical/Ingredient)
Identifiers: Product ID 17089-306_7e7be278-8d19-71c4-e053-2991aa0a377cSPL ID 7e7be278-8d19-71c4-e053-2991aa0a377cSPL set ID c5f4a798-e628-4388-a98d-7449dd92f2d6UNII YKH834O4BH, 8ID597Z82X, XTC0D02P6C, 63O327782Q, 49NGK53TPQ, 6DY04L71DR, 810258W28U, Q28R5GF371, 88XHZ13131, 817L1N4CKP, JL5DK93RCL, T5L8T28FGP, C8CV8867O8, HQJ5Z3SOIV, 68Y4CF58BV, P4A66LQ3QJ, 6YR2608RSU, M572600E5PUPC 0317089306184
Pharmacologic class: Antimalarial; Catecholamine; Melanin Synthesis Inhibitor; Non-Standardized Plant Allergenic Extract; Vitamin B6 Analog; alpha-Adrenergic Agonist; beta-Adrenergic Agonist

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

N417089030618 followed by a unit qualifier and the quantity

Package 17089-0306-18. 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)

Take 15 minutes before meals

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)