What is NDC 17089-293?

17089-293 is the product NDC for Guna-Bowel, Aloe 2 [hp_X]/30mL + 18 more ingredients solution/ drops, 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-Bowel (Aloe - aluminum oxide - bryonia alba root - chelidonium majus - cholecalciferol - collinsonia - frangula alnus bark - niacin - pantothenic acid - potassium carbonate - rhubarb - silybum marianum seed - skatole - sodium carbonate - strychnos nux-vomica seed - sus scrofa colon - sus scrofa rectum - taraxacum officinale - thiamine -).

What is the active ingredient?

Aloe, Aluminum oxide, Bryonia alba root, Silybum marianum seed, Chelidonium majus, Cholecalciferol, Collinsonia, Sus scrofa colon, Potassium carbonate, Sodium carbonate, Niacin, Strychnos nux-vomica seed, Pantothenic acid, Sus scrofa rectum, Frangula alnus bark, Rhubarb, Skatole, Taraxacum officinale, Thiamine.

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-Bowel?

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-Bowel NDC 17089-293 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-293Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0293Add 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
17089-293-18	1708902931817089029318	1 BOTTLE, DROPPER in 1 BOX (17089-293-18) / 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-Bowel
Generic name (nonproprietary): aloe - aluminum oxide - bryonia alba root - chelidonium majus - cholecalciferol - collinsonia - frangula alnus bark - niacin - pantothenic acid - potassium carbonate - rhubarb - silybum marianum seed - skatole - sodium carbonate - strychnos nux-vomica seed - sus scrofa colon - sus scrofa rectum - taraxacum officinale - thiamine -
Active ingredients: Aloe — 2 [hp_X]/30mLAluminum oxide — 6 [hp_X]/30mLBryonia alba root — 6 [hp_X]/30mLSilybum marianum seed — 2 [hp_X]/30mLChelidonium majus — 2 [hp_X]/30mLCholecalciferol — 2 [hp_X]/30mLCollinsonia — 2 [hp_X]/30mLSus scrofa colon — 12 [hp_X]/30mLPotassium carbonate — 6 [hp_X]/30mLSodium carbonate — 6 [hp_X]/30mLNiacin — 2 [hp_X]/30mLStrychnos nux-vomica seed — 6 [hp_X]/30mLPantothenic acid — 2 [hp_X]/30mLSus scrofa rectum — 12 [hp_X]/30mLFrangula alnus bark — 2 [hp_X]/30mLRhubarb — 2 [hp_X]/30mLSkatole — 10 [hp_X]/30mLTaraxacum officinale — 2 [hp_X]/30mLThiamine — 4 [hp_X]/30mL
Dosage form: Solution/ drops
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
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Nicotinic Acids (Chemical structure)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Vitamin D (Chemical structure)
Identifiers: Product ID 17089-293_53e95cf4-56b0-8501-e063-6294a90a3eddSPL ID 53e95cf4-56b0-8501-e063-6294a90a3eddSPL set ID 75465821-a889-4697-b470-e9588a523205UNII V5VD430YW9, LMI26O6933, T7J046YI2B, U946SH95EE, 7E889U5RNN, 1C6V77QF41, 94J255A0UC, BQN1B9B9HA, 45P3261C7T, 2679MF687A, 269XH13919, 19F5HK2737, QV1358E70N, S2D77IH61R, G280W4MW6E, 9W945B5H7R, 39981FM375, X66NSO3N35UPC 0317089293187
Pharmacologic class: Nicotinic Acid; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Vitamin D

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

N417089029318 followed by a unit qualifier and the quantity

Package 17089-0293-18. 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 10, 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)

About NDC 17089-293

What is NDC 17089-293?: 17089-293 is the product NDC for Guna-Bowel, Aloe 2 [hp_X]/30mL + 18 more ingredients solution/ drops, 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-Bowel (Aloe - aluminum oxide - bryonia alba root - chelidonium majus - cholecalciferol - collinsonia - frangula alnus bark - niacin - pantothenic acid - potassium carbonate - rhubarb - silybum marianum seed - skatole - sodium carbonate - strychnos nux-vomica seed - sus scrofa colon - sus scrofa rectum - taraxacum officinale - thiamine -).
What is the active ingredient?: Aloe, Aluminum oxide, Bryonia alba root, Silybum marianum seed, Chelidonium majus, Cholecalciferol, Collinsonia, Sus scrofa colon, Potassium carbonate, Sodium carbonate, Niacin, Strychnos nux-vomica seed, Pantothenic acid, Sus scrofa rectum, Frangula alnus bark, Rhubarb, Skatole, Taraxacum officinale, Thiamine.
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-Bowel?: 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.