What is NDC 17089-452?

17089-452 is the product NDC for Guna-Oral, Aconitum napellus 3 [hp_X]/30mL + 10 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-Oral (Achillea millefolium - aconitum napellus - arnica montana - atropa belladonna - calcium sulfide - comfrey root - echinacea angustifolia - echinacea purpurea - hypericum perforatum - sus scrofa tooth - witch hazel -).

What is the active ingredient?

Aconitum napellus, Arnica montana, Atropa belladonna, Echinacea angustifolia, Echinacea purpurea, Witch hazel, Calcium sulfide, Hypericum perforatum, Achillea millefolium, Comfrey root, Sus scrofa tooth.

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-Oral?

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-Oral NDC 17089-452 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-452Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0452Add 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
17089-452-27	1708904522717089045227	1 BOTTLE, SPRAY in 1 BOX (17089-452-27) / 50 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-Oral
Generic name (nonproprietary): achillea millefolium - aconitum napellus - arnica montana - atropa belladonna - calcium sulfide - comfrey root - echinacea angustifolia - echinacea purpurea - hypericum perforatum - sus scrofa tooth - witch hazel -
Active ingredients: Aconitum napellus — 3 [hp_X]/30mLArnica montana — 3 [hp_X]/30mLAtropa belladonna — 4 [hp_X]/30mLEchinacea angustifolia — 2 [hp_X]/30mLEchinacea purpurea — 2 [hp_X]/30mLWitch hazel — 2 [hp_X]/30mLCalcium sulfide — 6 [hp_X]/30mLHypericum perforatum — 3 [hp_X]/30mLAchillea millefolium — 3 [hp_X]/30mLComfrey root — 6 [hp_X]/30mLSus scrofa tooth — 12 [hp_X]/30mL
Dosage form: Spray
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
Identifiers: Product ID 17089-452_7e8ff906-fbc2-e1bf-e053-2a91aa0a3326SPL ID 7e8ff906-fbc2-e1bf-e053-2a91aa0a3326SPL set ID f1b8e5ab-8689-4bf2-a6d9-863d02f29579UNII U0NQ8555JD, O80TY208ZW, WQZ3G9PF0H, VB06AV5US8, QI7G114Y98, 101I4J0U34, 1MBW07J51Q, XK4IUX8MNB, 2FXJ6SW4PK, M9VVZ08EKQ, V69U5FL51FUPC 0317089452270

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

N417089045227 followed by a unit qualifier and the quantity

Package 17089-0452-27. 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)

Directions : Rotate the nebulizer to the upright position. Spray onto affected areas: mouth, throat or gingiva as needed.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 17089-452

What is NDC 17089-452?: 17089-452 is the product NDC for Guna-Oral, Aconitum napellus 3 [hp_X]/30mL + 10 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-Oral (Achillea millefolium - aconitum napellus - arnica montana - atropa belladonna - calcium sulfide - comfrey root - echinacea angustifolia - echinacea purpurea - hypericum perforatum - sus scrofa tooth - witch hazel -).
What is the active ingredient?: Aconitum napellus, Arnica montana, Atropa belladonna, Echinacea angustifolia, Echinacea purpurea, Witch hazel, Calcium sulfide, Hypericum perforatum, Achillea millefolium, Comfrey root, Sus scrofa tooth.
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-Oral?: 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.