What is NDC 17089-473?

17089-473 is the product NDC for Guna Osteo, Arnica montana root 3 [hp_X]/30mL + 10 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 Osteo (Arnica montana root - CALCIUM FLUORIDE - CALCIUM PHOSPHATE - equisetum hyemale - fumaric acid - SUS SCROFA UMBILICAL CORD - sus scrofa ovary - sus scrofa placenta - comfrey root - succinic acid - silicon dioxide -).

What is the active ingredient?

Arnica montana root, Fumaric acid, Sus scrofa umbilical cord, Sus scrofa ovary, Sus scrofa placenta, Comfrey root, Succinic acid, Silicon dioxide, Calcium fluoride, Calcium phosphate, Equisetum hyemale.

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 Osteo?

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 Osteo NDC 17089-473 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-473Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0473Add 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
17089-473-18	1708904731817089047318	1 BOTTLE, DROPPER in 1 BOX (17089-473-18) / 30 mL in 1 BOTTLE, DROPPERMarketed from Feb 17, 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 Osteo
Generic name (nonproprietary): arnica montana root - calcium fluoride - calcium phosphate - equisetum hyemale - fumaric acid - sus scrofa umbilical cord - sus scrofa ovary - sus scrofa placenta - comfrey root - succinic acid - silicon dioxide -
Active ingredients: Arnica montana root — 3 [hp_X]/30mLFumaric acid — 4 [hp_X]/30mLSus scrofa umbilical cord — 6 [hp_X]/30mLSus scrofa ovary — 6 [hp_X]/30mLSus scrofa placenta — 6 [hp_X]/30mLComfrey root — 6 [hp_X]/30mLSuccinic acid — 4 [hp_X]/30mLSilicon dioxide — 8 [hp_X]/30mLCalcium fluoride — 8 [hp_X]/30mLCalcium phosphate — 8 [hp_X]/30mLEquisetum hyemale — 3 [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: Feb 17, 2021
Listing expires: Dec 31, 2027
Other FDA classes: Calcium (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)
Identifiers: Product ID 17089-473_ba446257-56b6-616f-e053-2a95a90a1f16SPL ID ba446257-56b6-616f-e053-2a95a90a1f16SPL set ID ba4462d6-9751-530f-e053-2995a90a1f16UNII MUE8Y11327, 88XHZ13131, 118OYG6W3H, S7YTV04R8O, C8CV8867O8, M9VVZ08EKQ, AB6MNQ6J6L, ETJ7Z6XBU4, O3B55K4YKI, 97Z1WI3NDX, 59677RXH25
Pharmacologic class: Blood Coagulation Factor

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

N417089047318 followed by a unit qualifier and the quantity

Package 17089-0473-18. 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 Feb 17, 2021.

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 17089-473

What is NDC 17089-473?: 17089-473 is the product NDC for Guna Osteo, Arnica montana root 3 [hp_X]/30mL + 10 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 Osteo (Arnica montana root - CALCIUM FLUORIDE - CALCIUM PHOSPHATE - equisetum hyemale - fumaric acid - SUS SCROFA UMBILICAL CORD - sus scrofa ovary - sus scrofa placenta - comfrey root - succinic acid - silicon dioxide -).
What is the active ingredient?: Arnica montana root, Fumaric acid, Sus scrofa umbilical cord, Sus scrofa ovary, Sus scrofa placenta, Comfrey root, Succinic acid, Silicon dioxide, Calcium fluoride, Calcium phosphate, Equisetum hyemale.
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 Osteo?: 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.