Guna-Matrix NDC 17089-416

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-416Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0416Add 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
17089-416-18	17089041618	1 BOTTLE, DROPPER in 1 BOX (17089-416-18) / 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-Matrix
Generic name (nonproprietary): ascorbic acid - dodecahydroxycyclohexane dihydrate - fucus vesiculosus - histidine monohydrochloride - human interleukin-6 (nonglycosylated) - hyaluronidase - lactic acid, dl - malic acid - nadide - phenylalanine - prasterone - prolactin - rancid beef - sodium diethyl oxalacetate - sodium pyruvate - sodium sulfate - sus scrofa conjunctiva - sus scrofa small intestine mucosa lymph follicle - thuja occidentalis twig - tyrosine -
Active ingredients: Ascorbic acid — 4 [hp_X]/30mLSus scrofa conjunctiva — 6 [hp_X]/30mLPrasterone — 6 [hp_X]/30mLMalic acid — 6 [hp_X]/30mLFucus vesiculosus — 4 [hp_X]/30mLHistidine monohydrochloride — 4 [hp_X]/30mLHyaluronidase — 6 [hp_X]/30mLHuman interleukin-6 (Nonglycosylated) — 4 [hp_C]/30mLLactic acid, Dl- — 4 [hp_X]/30mLSus scrofa small intestine mucosa lymph follicle — 6 [hp_X]/30mLNadide — 6 [hp_X]/30mLSodium diethyl oxalacetate — 6 [hp_X]/30mLSodium pyruvate — 6 [hp_X]/30mLSodium sulfate — 12 [hp_X]/30mLPhenylalanine — 4 [hp_X]/30mLProlactin — 6 [hp_X]/30mLRancid beef — 12 [hp_X]/30mLThuja occidentalis leafy twig — 12 [hp_X]/30mLDodecahydroxycyclohexane dihydrate — 6 [hp_X]/30mLTyrosine — 4 [hp_X]/30mL
Dosage form: Solution/ drops
Route: Oral
Labeler: Guna spa
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 27, 2010
Listing expires: Dec 31, 2027
Other FDA classes: Ascorbic Acid (Chemical structure)Glycoside Hydrolases (Chemical structure)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)
Identifiers: Product ID 17089-416_53f5a156-3403-726e-e063-6394a90a1111SPL ID 53f5a156-3403-726e-e063-6394a90a1111SPL set ID fa9ed512-97dc-44a2-b32d-86ca8c240532UNII PQ6CK8PD0R, W61ME6Q717, 459AG36T1B, 817L1N4CKP, 535G2ABX9M, 1D5Q932XM6, 8KOG53Z5EM, 92QVL9080Y, 3B8D35Y7S4, 308LM01C72, 0U46U6E8UK, 6CA025Y4FG, POD38AIF08, 0YPR65R21J, 47E5O17Y3R, 2S58538ZG2, 29SUH5R3HU, 1NT28V9397, 5BWD2J7B4W, 42HK56048UUPC 0317089416180
Pharmacologic class: Endoglycosidase; 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

N417089041618 followed by a unit qualifier and the quantity

Package 17089-0416-18. 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 Jun 11, 2026.

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)