GUNA-BOWEL - 17089-293-18 - (ALOE - ALUMINUM OXIDE - BRYONIA ALBA ROOT - CHELIDONIUM MAJUS - CHOLECALCIFEROL - COLLINSONIA - FRANGULA ALNUS BARK - NIACIN - PANTOTHENIC ACID - POTASSIUM CARBONATE - RHUBARB - SILYBUM MARIANUM SEED)

Alphabetical Index


Drug Information of GUNA-BOWEL

Product NDC: 17089-293
Proprietary Name: GUNA-BOWEL
Non Proprietary Name: ALOE - ALUMINUM OXIDE - BRYONIA ALBA ROOT - CHELIDONIUM MAJUS - CHOLECALCIFEROL - COLLINSONIA - FRANGULA ALNUS BARK - NIACIN - PANTOTHENIC ACID - POTASSIUM CARBONATE - RHUBARB - SILYBUM MARIANUM SEED
Active Ingredient(s): 2; 6; 6; 2; 2; 2; 2; 2; 2; 6; 2; 2; 10; 6; 6; 12; 12; 2; 4    [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL & nbsp;   ALOE - ALUMINUM OXIDE - BRYONIA ALBA ROOT - CHELIDONIUM MAJUS - CHOLECALCIFEROL - COLLINSONIA - FRANGULA ALNUS BARK - NIACIN - PANTOTHENIC ACID - POTASSIUM CARBONATE - RHUBARB - SILYBUM MARIANUM SEED
Administration Route(s): ORAL
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of GUNA-BOWEL

Product NDC: 17089-293
Labeler Name: Guna spa
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20060523

Package Information of GUNA-BOWEL

Package NDC: 17089-293-18
Package Description: 1 BOTTLE, DROPPER in 1 BOX (17089-293-18) > 30 mL in 1 BOTTLE, DROPPER

NDC Information of GUNA-BOWEL

NDC Code 17089-293-18
Proprietary Name GUNA-BOWEL
Package Description 1 BOTTLE, DROPPER in 1 BOX (17089-293-18) > 30 mL in 1 BOTTLE, DROPPER
Product NDC 17089-293
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ALOE - ALUMINUM OXIDE - BRYONIA ALBA ROOT - CHELIDONIUM MAJUS - CHOLECALCIFEROL - COLLINSONIA - FRANGULA ALNUS BARK - NIACIN - PANTOTHENIC ACID - POTASSIUM CARBONATE - RHUBARB - SILYBUM MARIANUM SEED
Dosage Form Name SOLUTION/ DROPS
Route Name ORAL
Start Marketing Date 20060523
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Guna spa
Substance Name 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
Strength Number 2; 6; 6; 2; 2; 2; 2; 2; 2; 6; 2; 2; 10; 6; 6; 12; 12; 2; 4
Strength Unit [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL
Pharmaceutical Classes

Complete Information of GUNA-BOWEL


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