Guna Matrix Detox NDC 17089-460

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-460Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0460Add 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
17089-460-18	17089046018	1 BOTTLE, DROPPER in 1 BOX (17089-460-18) / 30 mL in 1 BOTTLE, DROPPERMarketed from Jul 14, 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 Matrix Detox
Generic name (nonproprietary): sodium sulfate - podophyllum peltatum root - solidago virgaurea flowering top - apis mellifera - equisetum hyemale - strychnos nux vomica seed - hamamelis virginiana root bark stem bark - lycopodium clavatum spore - galium aparine whole - thuja occidentalis leafy twig - berberis vulgaris root bark - myosotis arvensis - chelidonium majus whole - fucus vesiculosus -
Active ingredients: Fucus vesiculosus — 6 [hp_X]/30mLSus scrofa vein — 6 [hp_X]/30mLGalium aparine whole — 4 [hp_X]/30mLThuja occidentalis leafy twig — 6 [hp_X]/30mLConium maculatum flowering top — 3 [hp_X]/30mLMyosotis arvensis — 4 [hp_X]/30mLSodium pyruvate — 3 [hp_X]/30mLMalic acid — 6 [hp_X]/30mLGraphite — 12 [hp_X]/30mLSilicon dioxide — 8 [hp_X]/30mLSodium sulfate — 12 [hp_X]/30mLSodium diethyl oxalacetate — 3 [hp_X]/30mLSolidago virgaurea flowering top — 2 [hp_X]/30mLUrtica urens whole — 6 [hp_X]/30mLRancid beef — 12 [hp_X]/30mL
Dosage form: Solution/ drops
Route: Oral
Labeler: Guna spa
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 14, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)
Identifiers: Product ID 17089-460_b2587436-faab-37c8-e053-2995a90a3fbaSPL ID b2587436-faab-37c8-e053-2995a90a3fbaSPL set ID a369b95b-4d57-f149-e053-2995a90a87e3UNII 535G2ABX9M, 2510RH3I89, Z4B6561488, 1NT28V9397, Q28R5GF371, C73BK97H5J, POD38AIF08, 817L1N4CKP, 4QQN74LH4O, ETJ7Z6XBU4, 0YPR65R21J, 6CA025Y4FG, 5405K23S50, IHN2NQ5OF9, 29SUH5R3HUUPC 0317089460183
Pharmacologic class: Osmotic Laxative

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

N417089046018 followed by a unit qualifier and the quantity

Package 17089-0460-18. 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)