What is NDC 17089-418?

17089-418 is the product NDC for Guna-Allergy T, Epinephrine 6 [hp_X]/30mL + 16 more ingredients solution/ drops, listed with the FDA by Guna spa. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Guna-Allergy T (Ammonium carbonate - apis mellifera - arsenic trioxide - blatta orientalis - cupric acetate - drimia maritima bulb - epinephrine - galphimia glauca flowering top - histamine dihydrochloride - luffa operculata - manganese gluconate - onion - schoenocaulon officinale seed - sodium chloride - sus scrofa adrenal gland - sus scrofa bronchus - sus scrofa nasal mucosa -).

What is the active ingredient?

Epinephrine, Onion, Ammonium carbonate, Apis mellifera, Arsenic trioxide, Blatta orientalis, Sus scrofa bronchus, Cupric acetate, Galphimia glauca flowering top, Sus scrofa adrenal gland, Histamine dihydrochloride, Luffa operculata fruit, Manganese gluconate, Sus scrofa nasal mucosa, Sodium chloride, Schoenocaulon officinale seed, Drimia maritima bulb.

Guna spa, NDC labeler code 17089. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Guna-Allergy T?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Guna-Allergy T NDC 17089-418 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-418Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0418Add 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
17089-418-18	1708904181817089041818	1 BOTTLE, DROPPER in 1 BOX (17089-418-18) / 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 T
Generic name (nonproprietary): ammonium carbonate - apis mellifera - arsenic trioxide - blatta orientalis - cupric acetate - drimia maritima bulb - epinephrine - galphimia glauca flowering top - histamine dihydrochloride - luffa operculata - manganese gluconate - onion - schoenocaulon officinale seed - sodium chloride - sus scrofa adrenal gland - sus scrofa bronchus - sus scrofa nasal mucosa -
Active ingredients: Epinephrine — 6 [hp_X]/30mLOnion — 30 [hp_X]/30mLAmmonium carbonate — 30 [hp_X]/30mLApis mellifera — 200 [hp_X]/30mLArsenic trioxide — 30 [hp_X]/30mLBlatta orientalis — 12 [hp_X]/30mLSus scrofa bronchus — 200 [hp_X]/30mLCupric acetate — 30 [hp_X]/30mLGalphimia glauca flowering top — 12 [hp_X]/30mLSus scrofa adrenal gland — 12 [hp_X]/30mLHistamine dihydrochloride — 200 [hp_X]/30mLLuffa operculata fruit — 12 [hp_X]/30mLManganese gluconate — 4 [hp_X]/30mLSus scrofa nasal mucosa — 200 [hp_X]/30mLSodium chloride — 30 [hp_X]/30mLSchoenocaulon officinale seed — 30 [hp_X]/30mLDrimia maritima bulb — 30 [hp_X]/30mL
Dosage form: Solution/ drops
Route: Oral
Labeler: Guna spaNDC labeler code 17089
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 27, 2010
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic alpha-Agonists (Mechanism)Adrenergic beta-Agonists (Mechanism)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Bee Venoms (Chemical structure)Catecholamines (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)Insect Proteins (Chemical structure)Magnetic Resonance Contrast Activity (Mechanism)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 17089-418_53ea3900-f754-760c-e063-6294a90af2d2SPL ID 53ea3900-f754-760c-e063-6294a90af2d2SPL set ID fddba85e-2bec-468f-a01a-b71a3aeed9d3UNII YKH834O4BH, 492225Q21H, NJ5VT0FKLJ, 7S82P3R43Z, S7V92P67HO, 535787266D, K34664156J, 39M11XPH03, 93PH5Q8M7E, 398IYQ16YV, 3POA0Q644U, C4MO6809HU, 9YY2F980SV, ID3Z1X61WY, 451W47IQ8X, 6NAF1689IO, 3629601H5D
Pharmacologic class: Catecholamine; Non-Standardized Food Allergenic Extract; Non-Standardized Insect Allergenic Extract; Paramagnetic Contrast Agent; Standardized Insect Venom Allergenic Extract; 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

N417089041818 followed by a unit qualifier and the quantity

Package 17089-0418-18. 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)

About NDC 17089-418

What is NDC 17089-418?: 17089-418 is the product NDC for Guna-Allergy T, Epinephrine 6 [hp_X]/30mL + 16 more ingredients solution/ drops, listed with the FDA by Guna spa. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Guna-Allergy T (Ammonium carbonate - apis mellifera - arsenic trioxide - blatta orientalis - cupric acetate - drimia maritima bulb - epinephrine - galphimia glauca flowering top - histamine dihydrochloride - luffa operculata - manganese gluconate - onion - schoenocaulon officinale seed - sodium chloride - sus scrofa adrenal gland - sus scrofa bronchus - sus scrofa nasal mucosa -).
What is the active ingredient?: Epinephrine, Onion, Ammonium carbonate, Apis mellifera, Arsenic trioxide, Blatta orientalis, Sus scrofa bronchus, Cupric acetate, Galphimia glauca flowering top, Sus scrofa adrenal gland, Histamine dihydrochloride, Luffa operculata fruit, Manganese gluconate, Sus scrofa nasal mucosa, Sodium chloride, Schoenocaulon officinale seed, Drimia maritima bulb.
Who is the labeler?: Guna spa, NDC labeler code 17089. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Guna-Allergy T?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.