Guna-Allergy-Prev NDC 17089-299

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-299Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0299Add 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
17089-299-18	17089029918	1 BOTTLE, DROPPER in 1 BOX (17089-299-18) / 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-Allergy-Prev
Generic name (nonproprietary): ambrosia artemisiifolia - anguilla rostrata blood serum - arundo pliniana root - black currant - chelidonium majus - citric acid monohydrate - histamine dihydrochloride - human interleukin 12 - interferon gamma-1b - manganese gluconate - parietaria officinalis - phleum pratense - sodium pyruvate - sodium sulfate - succinic acid - sulfur - urtica urens - viburnum opulus root - wyethia helenioides root -
Active ingredients: Ambrosia artemisiifolia — 18 [hp_X]/30mLArundo pliniana root — 18 [hp_X]/30mLAsclepias curassavica — 6 [hp_X]/30mLBlack currant — 1 [hp_X]/30mLCitric acid monohydrate — 6 [hp_X]/30mLHistamine dihydrochloride — 30 [hp_X]/30mLInterferon gamma-1b — 4 [hp_C]/30mLHuman interleukin 12 — 4 [hp_C]/30mLManganese gluconate — 4 [hp_X]/30mLSodium pyruvate — 6 [hp_X]/30mLSodium sulfate — 200 [hp_X]/30mLParietaria officinalis — 18 [hp_X]/30mLPhleum pratense — 18 [hp_X]/30mLAnguilla rostrata blood serum — 200 [hp_X]/30mLSuccinic acid — 6 [hp_X]/30mLSulfur — 30 [hp_X]/30mLUrtica urens — 18 [hp_X]/30mLViburnum opulus root — 3 g/30mLWyethia helenioides root — 18 [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: Acidifying Activity (Mechanism)Calcium Chelating Activity (Mechanism)Decreased Coagulation Factor Activity (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Interferon-gamma (Chemical structure)Magnetic Resonance Contrast Activity (Mechanism)Osmotic Activity (Mechanism)
Identifiers: Product ID 17089-299_7e029048-a7aa-68a5-e053-2a91aa0af0beSPL ID 7e029048-a7aa-68a5-e053-2a91aa0af0beSPL set ID adae93c0-1de9-4e45-ab58-148171f0dc86UNII 9W34L2CQ9A, ZXE7LB03WC, JSZ93E47EP, 9755T40D11, 2968PHW8QP, 3POA0Q644U, 21K6M2I7AG, 7B590791ER, 9YY2F980SV, POD38AIF08, 0YPR65R21J, 0P46LFE4VC, L7B16ESD1U, AB6MNQ6J6L, 70FD1KFU70, IHN2NQ5OF9, 6N0G8XY3T8, J10PD1AQ0NUPC 0317089299189
Pharmacologic class: Anti-coagulant; Calculi Dissolution Agent; Interferon gamma; Osmotic Laxative; Paramagnetic Contrast Agent

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

N417089029918 followed by a unit qualifier and the quantity

Package 17089-0299-18. 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)