Guna Bowel Plus NDC 17089-470

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-470Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0470Add 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
17089-470-18	17089047018	1 BOTTLE, DROPPER in 1 BOX (17089-470-18) / 30 mL in 1 BOTTLE, DROPPERMarketed from Jan 17, 2021

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 Plus
Generic name (nonproprietary): activated charcoal - aloe - aluminum oxide - bryonia alba root - chelidonium majus - collinsonia - frangula alnus bark - lycopodium clavatum spore - potassium carbonate- rhubarb - strychnos nux vomica seed - silybum marianum seed - skatole - sodium carbonate - sus scrofa pancreas - taraxacum officinale - thiamine -
Active ingredients: Aloe — 4 [hp_X]/30mLAluminum oxide — 6 [hp_X]/30mLBryonia alba root — 6 [hp_X]/30mLSilybum marianum seed — 2 [hp_X]/30mLChelidonium majus — 2 [hp_X]/30mLActivated charcoal — 6 [hp_X]/30mLCollinsonia — 2 [hp_X]/30mLSus scrofa pancreas — 6 [hp_X]/30mLPotassium carbonate — 6 [hp_X]/30mLSodium carbonate — 6 [hp_X]/30mLLycopodium clavatum spore — 2 [hp_X]/30mLStrychnos nux-vomica seed — 6 [hp_X]/30mLFrangula alnus bark — 2 [hp_X]/30mLRhubarb — 2 [hp_X]/30mLSkatole — 6 [hp_X]/30mLTaraxacum officinale — 2 [hp_X]/30mLThiamine — 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: Jan 17, 2021
Listing expires: Dec 31, 2026
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)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 17089-470_b3aa6401-9af7-b0d5-e053-2995a90a10efSPL ID b3aa6401-9af7-b0d5-e053-2995a90a10efSPL set ID b3aa4fd3-c87a-ccd2-e053-2995a90a46a9UNII V5VD430YW9, LMI26O6933, T7J046YI2B, U946SH95EE, 7E889U5RNN, 2P3VWU3H10, 9Y3J3362RY, BQN1B9B9HA, 45P3261C7T, C88X29Y479, 269XH13919, S2D77IH61R, G280W4MW6E, 9W945B5H7R, 39981FM375, X66NSO3N35
Pharmacologic class: Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract

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

N417089047018 followed by a unit qualifier and the quantity

Package 17089-0470-18. 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 Jan 17, 2021.

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)