What is NDC 17089-451?

17089-451 is the product NDC for Guna-Sinus Nose, Onion 8 [hp_X]/30mL + 20 more ingredients spray, 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-Sinus Nose (Althaea officinalis leaf - ascorbic acid - black currant - calcium sulfide - copper - echinacea angustifolia - goldenseal - lachesis muta venom - lobaria pulmonaria - manganese - mercuric sulfide - onion - plantago major - potassium carbonate - pulsatilla vulgaris - silicon dioxide - silver nitrate - sinusitisinum - sus scrofa nasal mucosa - sus scrofa thymus - sus scrofa urinary bladder -).

What is the active ingredient?

Onion, Althaea officinalis leaf, Silver nitrate, Ascorbic acid, Black currant, Lobaria pulmonaria, Copper, Echinacea angustifolia, Calcium sulfide, Goldenseal, Potassium dichromate, Lachesis muta venom, Manganese, Mercuric sulfide, Sus scrofa nasal mucosa, Plantago major, Pulsatilla vulgaris, Silicon dioxide, Sinusitisinum, Sus scrofa thymus, Sus scrofa urinary bladder.

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-Sinus Nose?

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-Sinus Nose NDC 17089-451 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-451Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0451Add 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
17089-451-23	1708904512317089045123	1 BOTTLE, SPRAY in 1 BOX (17089-451-23) / 30 mL in 1 BOTTLE, SPRAYMarketed 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-Sinus Nose
Generic name (nonproprietary): althaea officinalis leaf - ascorbic acid - black currant - calcium sulfide - copper - echinacea angustifolia - goldenseal - lachesis muta venom - lobaria pulmonaria - manganese - mercuric sulfide - onion - plantago major - potassium carbonate - pulsatilla vulgaris - silicon dioxide - silver nitrate - sinusitisinum - sus scrofa nasal mucosa - sus scrofa thymus - sus scrofa urinary bladder -
Active ingredients: Onion — 8 [hp_X]/30mLAlthaea officinalis leaf — 2 [hp_X]/30mLSilver nitrate — 10 [hp_X]/30mLAscorbic acid — 2 [hp_X]/30mLBlack currant — 1 [hp_X]/30mLLobaria pulmonaria — 2 [hp_X]/30mLCopper — 3 [hp_X]/30mLEchinacea angustifolia — 3 [hp_X]/30mLCalcium sulfide — 8 [hp_X]/30mLGoldenseal — 8 [hp_X]/30mLPotassium dichromate — 8 [hp_X]/30mLLachesis muta venom — 30 [hp_X]/30mLManganese — 3 [hp_X]/30mLMercuric sulfide — 8 [hp_X]/30mLSus scrofa nasal mucosa — 12 [hp_X]/30mLPlantago major — 2 [hp_X]/30mLPulsatilla vulgaris — 8 [hp_X]/30mLSilicon dioxide — 8 [hp_X]/30mLSinusitisinum — 30 [hp_X]/30mLSus scrofa thymus — 12 [hp_X]/30mLSus scrofa urinary bladder — 30 [hp_X]/30mL
Dosage form: Spray
Route: Nasal
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: Allergens (Chemical structure)Ascorbic Acid (Chemical structure)Cell-mediated Immunity (Physiologic effect)Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 17089-451_7d9d997a-fda9-2a63-e053-2a91aa0a0000SPL ID 7d9d997a-fda9-2a63-e053-2a91aa0a0000SPL set ID 36fef678-17c6-4d2a-a0f0-ddb298611f25UNII 492225Q21H, E2QQV92338, 95IT3W8JZE, PQ6CK8PD0R, 9755T40D11, D1YM0P5Z2T, 789U1901C5, VB06AV5US8, 1MBW07J51Q, ZW3Z11D0JV, T4423S18FM, VSW71SS07I, 42Z2K6ZL8P, ZI0T668SF1, ID3Z1X61WY, W2469WNO6U, I76KB35JEV, ETJ7Z6XBU4, B575563DM5, 7B69B0BD62, 3G7U72W8DAUPC 0317089451235
Pharmacologic class: Copper-containing Intrauterine Device; Non-Standardized Food Allergenic Extract; Vitamin C

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. Nasal products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N417089045123 followed by a unit qualifier and the quantity

Package 17089-0451-23. 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 22, 2018.

Indications (excerpt from the label)

Directions : tilt head slightly forward, place tip of bottle into nose, compress bottle once for each spray, aiming towards the back of the nose.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 17089-451

What is NDC 17089-451?: 17089-451 is the product NDC for Guna-Sinus Nose, Onion 8 [hp_X]/30mL + 20 more ingredients spray, 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-Sinus Nose (Althaea officinalis leaf - ascorbic acid - black currant - calcium sulfide - copper - echinacea angustifolia - goldenseal - lachesis muta venom - lobaria pulmonaria - manganese - mercuric sulfide - onion - plantago major - potassium carbonate - pulsatilla vulgaris - silicon dioxide - silver nitrate - sinusitisinum - sus scrofa nasal mucosa - sus scrofa thymus - sus scrofa urinary bladder -).
What is the active ingredient?: Onion, Althaea officinalis leaf, Silver nitrate, Ascorbic acid, Black currant, Lobaria pulmonaria, Copper, Echinacea angustifolia, Calcium sulfide, Goldenseal, Potassium dichromate, Lachesis muta venom, Manganese, Mercuric sulfide, Sus scrofa nasal mucosa, Plantago major, Pulsatilla vulgaris, Silicon dioxide, Sinusitisinum, Sus scrofa thymus, Sus scrofa urinary bladder.
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-Sinus Nose?: 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.