Guna Bowel Plus Solution/ Drops
NDC Package 17089-470-18
Package Information
Guna Bowel Plus (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 -) solution/ dropses is take 15 minutes before meals. This formulation utilizes a solution/ drops delivery system. Marketed by Guna Spa, this product is identified by NDC 17089-470.
Identification & Billing
Clinical Specifications
- ACTIVATED CHARCOAL 6 [hp_X]/30mL
- ALOE 4 [hp_X]/30mL
- ALUMINUM OXIDE 6 [hp_X]/30mL
- BRYONIA ALBA ROOT 6 [hp_X]/30mL
- CHELIDONIUM MAJUS 2 [hp_X]/30mL
- COLLINSONIA 2 [hp_X]/30mL
- FRANGULA ALNUS BARK 2 [hp_X]/30mL
- LYCOPODIUM CLAVATUM SPORE 2 [hp_X]/30mL
- POTASSIUM CARBONATE 6 [hp_X]/30mL
- RHUBARB 2 [hp_X]/30mL
- SILYBUM MARIANUM SEED 2 [hp_X]/30mL
- SKATOLE 6 [hp_X]/30mL
- SODIUM CARBONATE 6 [hp_X]/30mL
- STRYCHNOS NUX-VOMICA SEED 6 [hp_X]/30mL
- SUS SCROFA PANCREAS 6 [hp_X]/30mL
- TARAXACUM OFFICINALE 2 [hp_X]/30mL
- THIAMINE 4 [hp_X]/30mL
- Allergens - [CS]
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Seed Storage Proteins - [CS]
Regulatory & Marketing
Hierarchy Structure
- 17089 - Guna Spa
- 17089-470 - Guna Bowel Plus
- 17089-470-18 - 1 BOTTLE, DROPPER in 1 BOX / 30 mL in 1 BOTTLE, DROPPER
- 17089-470 - Guna Bowel Plus
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 17089-470-18 identifies a specific commercial package of 1 bottle, dropper in 1 box / 30 ml in 1 bottle, dropper of Guna Bowel Plus, a human over the counter drug labeled by Guna Spa. This solution/ drops is formulated for oral use and contains activated charcoal; aloe; aluminum oxide; bryonia alba root; chelidonium majus; collinsonia; frangula alnus bark; lycopodium clavatum spore; potassium carbonate; rhubarb; silybum marianum seed; skatole; sodium carbonate; strychnos nux-vomica seed; sus scrofa pancreas; taraxacum officinale; thiamine as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Guna Spa on January 17, 2021. The current certification is valid through December 31, 2026.
How is this Guna Spa product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 17089047018. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.