What is NDC 17089-235?

17089-235 is the product NDC for Guna-Tonsils, Angelica sinensis root 3 [hp_X]/4g + 10 more ingredients pellet, 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-Tonsils (Angelica sinensis root - binetrakin - interleukin-3 - lenograstim - melatonin - reishi - shiitake mushroom - sus scrofa blood - sus scrofa small intestine mucosa lymph follicle - sus scrofa spleen - interleukin-11 -).

What is the active ingredient?

Angelica sinensis root, Sus scrofa blood, Lenograstim, Interleukin-11, Interleukin-3, Binetrakin, Shiitake mushroom, Reishi, Sus scrofa small intestine mucosa lymph follicle, Melatonin, Sus scrofa spleen.

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-Tonsils?

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-Tonsils NDC 17089-235 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-235Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0235Add 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
17089-235-20	1708902352017089023520	2 TUBE in 1 BOX (17089-235-20) / 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-Tonsils
Generic name (nonproprietary): angelica sinensis root - binetrakin - interleukin-3 - lenograstim - melatonin - reishi - shiitake mushroom - sus scrofa blood - sus scrofa small intestine mucosa lymph follicle - sus scrofa spleen - interleukin-11 -
Active ingredients: Angelica sinensis root — 3 [hp_X]/4gSus scrofa blood — 7 [hp_C]/4gLenograstim — 4 [hp_C]/4gInterleukin-11 — 5 [hp_C]/4gInterleukin-3 — 5 [hp_C]/4gBinetrakin — 4 [hp_C]/4gShiitake mushroom — 8 [hp_X]/4gReishi — 8 [hp_X]/4gSus scrofa small intestine mucosa lymph follicle — 4 [hp_C]/4gMelatonin — 4 [hp_C]/4gSus scrofa spleen — 4 [hp_C]/4g
Dosage form: Pellet
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
Identifiers: Product ID 17089-235_7e8f9d55-ff7c-cbe7-e053-2a91aa0a382eSPL ID 7e8f9d55-ff7c-cbe7-e053-2a91aa0a382eSPL set ID b7d0a24f-c702-4b4a-8494-a4cbbb020257UNII B66F4574UG, 994R458ECK, 6WS4C399GB, O14Q7A13PT, VPB6TR49WU, 751635Z921, 1A64QN2D2F, TKD8LH0X2Z, 308LM01C72, JL5DK93RCL, 92AMN5J79YUPC 0317089235200

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

N417089023520 followed by a unit qualifier and the quantity

Package 17089-0235-20. 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)

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)

About NDC 17089-235

What is NDC 17089-235?: 17089-235 is the product NDC for Guna-Tonsils, Angelica sinensis root 3 [hp_X]/4g + 10 more ingredients pellet, 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-Tonsils (Angelica sinensis root - binetrakin - interleukin-3 - lenograstim - melatonin - reishi - shiitake mushroom - sus scrofa blood - sus scrofa small intestine mucosa lymph follicle - sus scrofa spleen - interleukin-11 -).
What is the active ingredient?: Angelica sinensis root, Sus scrofa blood, Lenograstim, Interleukin-11, Interleukin-3, Binetrakin, Shiitake mushroom, Reishi, Sus scrofa small intestine mucosa lymph follicle, Melatonin, Sus scrofa spleen.
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-Tonsils?: 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.