Guna Arthro Relief NDC 17089-463

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-463Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0463Add 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
17089-463-18	17089046318	1 BOTTLE, DROPPER in 1 BOX (17089-463-18) / 30 mL in 1 BOTTLE, DROPPERMarketed from Sep 24, 2020

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 Relief
Generic name (nonproprietary): arteria suis - alpha ketoglutaricum acidum - alpha lipoicum acidum - ascorbicum acidum - barium oxalsuccinicum - bryonia alba - calcarea carbonica - cartilago suis - chlorinum - cimicifuga racemosa - colchicum autumnale - dulcamara - embryo suis - funiculus umbilicalis suis - glandula suprarenalis suis - nadidum - natrum oxalaceticum - natrum sulphuricum - placenta totalis suis - rhus toxicodendron - sulphur- vena suis -
Active ingredients: Oyster shell calcium carbonate, Crude — 4 [hp_X]/30mLSodium sulfate — 8 [hp_X]/30mL.alpha.-ketoglutaric acid — 3 [hp_X]/30mL.alpha.-lipoic acid — 8 [hp_X]/30mLSus scrofa artery — 6 [hp_X]/30mLAscorbic acid — 3 [hp_X]/30mLBarium oxalosuccinate — 6 [hp_X]/30mLBryonia alba root — 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 embryo — 6 [hp_X]/30mLSolanum dulcamara flower — 6 [hp_X]/30mLSus scrofa umbilical cord — 6 [hp_X]/30mLSus scrofa adrenal gland — 6 [hp_X]/30mLNadide — 3 [hp_X]/30mLSodium diethyl oxalacetate — 3 [hp_X]/30mLSus scrofa placenta — 6 [hp_X]/30mLToxicodendron pubescens leaf — 6 [hp_X]/30mLSulfur — 4 [hp_X]/30mLSus scrofa vein — 6 [hp_X]/30mL
Dosage form: Solution/ drops
Route: Oral
Labeler: Guna spa
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 24, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Ascorbic Acid (Chemical structure)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)
Identifiers: Product ID 17089-463_b258aa33-c259-1343-e053-2a95a90af0c0SPL ID b258aa33-c259-1343-e053-2a95a90af0c0SPL set ID aebb990a-65bc-54ed-e053-2995a90a5682UNII 2E32821G6I, 0YPR65R21J, 8ID597Z82X, 73Y7P0K73Y, 63O327782Q, PQ6CK8PD0R, L7A49804ZQ, T7J046YI2B, 73ECW5WG2F, 4R7X1O2820, K73E24S6X9, 993QHL78E6, 9928MC12VO, W6J1279A6K, 118OYG6W3H, 398IYQ16YV, 0U46U6E8UK, 6CA025Y4FG, C8CV8867O8, 6IO182RP7A, 70FD1KFU70, 2510RH3I89UPC 0317089463184
Pharmacologic class: Osmotic Laxative; 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

N417089046318 followed by a unit qualifier and the quantity

Package 17089-0463-18. 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 Oct 23, 2020.

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)