Guna Hay Fever Relief NDC 17089-476

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-476Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0476Add 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
17089-476-20	17089047620	2 TUBE in 1 BOX (17089-476-20) / 4 g in 1 TUBEMarketed from Feb 17, 2021
17089-476-21	17089047621	1 TUBE in 1 BOX (17089-476-21) / 4 g in 1 TUBEMarketed from Dec 15, 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 Hay Fever Relief
Generic name (nonproprietary): strychnos nux vomica seed - histamine dihydrochloride - manganese - schoenocaulon officinale seed - apis mellifera - arsenic trioxide - silver nitrate - onion - euphrasia stricta - galphimia glauca flowering top - sulfur -
Active ingredients: Strychnos nux-vomica seed — 4 [hp_X]/4gHistamine dihydrochloride — 200 [hp_X]/4gManganese — 8 [hp_X]/4gSchoenocaulon officinale seed — 6 [hp_X]/4gOnion — 30 [hp_X]/4gApis mellifera — 200 [hp_X]/4gSilver nitrate — 6 [hp_X]/4gEuphrasia stricta — 5 [hp_X]/4gGalphimia glauca flowering top — 4 [hp_X]/4gSulfur — 30 [hp_X]/4gArsenic trioxide — 30 [hp_X]/4g
Dosage form: Pellet
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
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 17089-476_d3322d60-dd44-8e96-e053-2995a90a54b0SPL ID d3322d60-dd44-8e96-e053-2995a90a54b0SPL set ID b8db4fc6-f235-6f2b-e053-2a95a90a186fUNII 269XH13919, 3POA0Q644U, 42Z2K6ZL8P, 6NAF1689IO, 492225Q21H, 7S82P3R43Z, 95IT3W8JZE, C9642I91WL, 93PH5Q8M7E, 70FD1KFU70, S7V92P67HOUPC 0317089476207
Pharmacologic class: Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Standardized Insect Venom Allergenic Extract

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

N417089047620 followed by a unit qualifier and the quantity

Package 17089-0476-20. 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 15, 2021.

Indications (excerpt from the label)

Temporarily relieves hay fever symptoms, such as: ● sneezing ● coughing ● inflamed, runny nose

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)