Guna-React NDC 17089-237

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-237Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0237Add 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
17089-237-20	17089023720	2 TUBE in 1 BOX (17089-237-20) / 4 g in 1 TUBEMarketed 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-React
Generic name (nonproprietary): angelica sinensis root - arnica montana - asian ginseng - echinacea angustifolia - fomitopsis pinicola fruiting body - interferon gamma-1b - paeonia officinalis root - pork liver - reishi - silybum marianum seed - sus scrofa small intestine mucosa lymph follicle - turmeric -
Active ingredients: Turmeric — 3 [hp_X]/4gAngelica sinensis root — 3 [hp_X]/4gArnica montana — 4 [hp_X]/4gSilybum marianum seed — 3 [hp_X]/4gEchinacea angustifolia — 3 [hp_X]/4gAsian ginseng — 1 [hp_X]/4gPork liver — 4 [hp_C]/4gInterferon gamma-1b — 4 [hp_C]/4gReishi — 8 [hp_X]/4gSus scrofa small intestine mucosa lymph follicle — 4 [hp_C]/4gPaeonia officinalis root — 3 [hp_X]/4gFomitopsis pinicola fruiting body — 8 [hp_X]/4g
Dosage form: Pellet
Route: Oral
Labeler: Guna spa
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 23, 2006
Listing expires: Dec 31, 2026
Other FDA classes: Interferon-gamma (Chemical structure)
Identifiers: Product ID 17089-237_7e7d6ebc-5974-b9fc-e053-2991aa0a2ae5SPL ID 7e7d6ebc-5974-b9fc-e053-2991aa0a2ae5SPL set ID c2b64907-1ae2-4686-b13c-847dbb84724eUNII 856YO1Z64F, B66F4574UG, O80TY208ZW, U946SH95EE, VB06AV5US8, CUQ3A77YXI, 6EC706HI7F, 21K6M2I7AG, TKD8LH0X2Z, 308LM01C72, 8R564U2E1P, 30D02U2IRNUPC 0317089237204
Pharmacologic class: Interferon gamma

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

N417089023720 followed by a unit qualifier and the quantity

Package 17089-0237-20. 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 Dec 21, 2018.

Indications (excerpt from the label)

Directions : Turn tube upside down and rotate cap to release pellets into cap. Unscrew cap and without touching pellets tip them into the mouth under the tongue. Allow to dissolve Take 15 minutes before meals.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)