What is NDC 17089-304?

17089-304 is the product NDC for Guna-Arthro, Sus scrofa artery 6 [hp_X]/30mL + 26 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-Arthro (.alpha.-ketoglutaric acid - alpha lipoic acid - ascorbic acid - barium oxalosuccinate - black cohosh - bryonia alba root - calcitonin human - chlorine - colchicum autumnale bulb - nadide -).

What is the active ingredient?

Sus scrofa artery, Ascorbic acid, Barium oxalosuccinate, Bryonia alba root, Calcitonin human, Sus scrofa cartilage, Chlorine, Black cohosh, Colchicum autumnale bulb, Sus scrofa conjunctiva, Solanum dulcamara flower, Velafermin, Sus scrofa umbilical cord, Sus scrofa adrenal gland, Nadide, Sodium diethyl oxalacetate, Nerve growth factor, Sus scrofa parathyroid gland, Sus scrofa placenta, Quinhydrone, Toxicodendron pubescens leaf, Strontium carbonate, Sulfur, Sus scrofa vein, Prasterone, .alpha.-ketoglutaric acid, .alpha.-lipoic acid.

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-Arthro?

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-Arthro NDC 17089-304 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-304Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0304Add 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
17089-304-18	1708903041817089030418	1 BOTTLE, DROPPER in 1 BOX (17089-304-18) / 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-Arthro
Generic name (nonproprietary): .alpha.-ketoglutaric acid - alpha lipoic acid - ascorbic acid - barium oxalosuccinate - black cohosh - bryonia alba root - calcitonin human - chlorine - colchicum autumnale bulb - nadide -
Active ingredients: Sus scrofa artery — 6 [hp_X]/30mLAscorbic acid — 3 [hp_X]/30mLBarium oxalosuccinate — 3 [hp_X]/30mLBryonia alba root — 6 [hp_X]/30mLCalcitonin human — 6 [hp_X]/30mLSus scrofa cartilage — 6 [hp_X]/30mLChlorine — 6 [hp_X]/30mLBlack cohosh — 6 [hp_X]/30mLColchicum autumnale bulb — 6 [hp_X]/30mLSus scrofa conjunctiva — 6 [hp_X]/30mLSolanum dulcamara flower — 6 [hp_X]/30mLVelafermin — 4 [hp_C]/30mLSus scrofa umbilical cord — 6 [hp_X]/30mLSus scrofa adrenal gland — 6 [hp_X]/30mLNadide — 3 [hp_X]/30mLSodium diethyl oxalacetate — 3 [hp_X]/30mLNerve growth factor — 4 [hp_C]/30mLSus scrofa parathyroid gland — 6 [hp_X]/30mLSus scrofa placenta — 6 [hp_X]/30mLQuinhydrone — 3 [hp_X]/30mLToxicodendron pubescens leaf — 6 [hp_X]/30mLStrontium carbonate — 6 [hp_X]/30mLSulfur — 3 [hp_X]/30mLSus scrofa vein — 6 [hp_X]/30mLPrasterone — 6 [hp_X]/30mL.alpha.-ketoglutaric acid — 3 [hp_X]/30mL.alpha.-lipoic acid — 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: May 23, 2006
Listing expires: Dec 31, 2027
Other FDA classes: Ascorbic Acid (Chemical structure)Depigmenting Activity (Physiologic effect)Melanin Synthesis Inhibitors (Mechanism)
Identifiers: Product ID 17089-304_ed806a9b-af06-d713-e053-2a95a90a9730SPL ID ed806a9b-af06-d713-e053-2a95a90a9730SPL set ID 45ad3f03-0ee8-438f-81e7-3ca772022c98UNII 63O327782Q, PQ6CK8PD0R, L7A49804ZQ, T7J046YI2B, I0IO929019, 73ECW5WG2F, 4R7X1O2820, K73E24S6X9, 993QHL78E6, W61ME6Q717, W6J1279A6K, 6Z25C35927, 118OYG6W3H, 398IYQ16YV, 0U46U6E8UK, 6CA025Y4FG, V7FWP1D62O, 2KBE35NE8S, C8CV8867O8, P4A66LQ3QJ, 6IO182RP7A, 41YPU4MMCA, 70FD1KFU70, 2510RH3I89, 459AG36T1B, 8ID597Z82X, 73Y7P0K73YUPC 0317089304180
Pharmacologic class: Melanin Synthesis Inhibitor; 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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N417089030418 followed by a unit qualifier and the quantity

Package 17089-0304-18. 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 Nov 15, 2022.

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 17089-304

What is NDC 17089-304?: 17089-304 is the product NDC for Guna-Arthro, Sus scrofa artery 6 [hp_X]/30mL + 26 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-Arthro (.alpha.-ketoglutaric acid - alpha lipoic acid - ascorbic acid - barium oxalosuccinate - black cohosh - bryonia alba root - calcitonin human - chlorine - colchicum autumnale bulb - nadide -).
What is the active ingredient?: Sus scrofa artery, Ascorbic acid, Barium oxalosuccinate, Bryonia alba root, Calcitonin human, Sus scrofa cartilage, Chlorine, Black cohosh, Colchicum autumnale bulb, Sus scrofa conjunctiva, Solanum dulcamara flower, Velafermin, Sus scrofa umbilical cord, Sus scrofa adrenal gland, Nadide, Sodium diethyl oxalacetate, Nerve growth factor, Sus scrofa parathyroid gland, Sus scrofa placenta, Quinhydrone, Toxicodendron pubescens leaf, Strontium carbonate, Sulfur, Sus scrofa vein, Prasterone, .alpha.-ketoglutaric acid, .alpha.-lipoic acid.
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-Arthro?: 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.