Label: 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 - solution/ drops
- NDC Code(s): 17089-293-18
- Packager: Guna spa
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated November 14, 2022
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ACTIVE INGREDIENTS/PURPOSE
ALOE SOCOTRINA 2X LAXATIVE
ALUMINA 6X 8X CONSTIPATION
BRYONIA ALBA 6X 8X SPASMOLYTIC
CARDUUS MARIANUS 2X SUPPORTS DIGESTION
CHELIDONIUM MAJUS 2X SUPPORTS DIGESTION
CHOLECALCIFEROL 2X ANTIOXIDANT
COLLINSONIA CANADENSIS 2X HEMORRHOIDS
COLON 6X 12X 30X STIMULATES DIGESTION
KALI CARBONICUM 6X 8X 12X BACK PAIN
NATRUM CARBONICUM 6X 8X 12X BLOATING AFTER EATING
NIACIN 2X REGULATES CHOLESTEROL
NUX VOMICA 6X 8X HELPS DIGESTION
PANTOTHENIC ACID 2X STIMULATES DIGESTION
RECTUM 6X 12X 30X STIMULATES DIGESTION
RHAMNUS FRANGULA 2X LAXATIVE
RHEUM 2X LAXATIVE
SKATOLUM 6X 10X LAXATIVE
TARAXACUM 2X LAXATIVE
THIAMINUM HYDROCHLORICUM 4X STIMULATES DIGESTION
- USES
- WARNINGS
- PREGNANCY
- WARNINGS
- DIRECTIONS
- QUESTIONS
- INACTIVE INGREDIENT
- INDICATIONS & USAGE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
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 - solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:17089-293 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALOE (UNII: V5VD430YW9) (ALOE - UNII:V5VD430YW9) ALOE 2 [hp_X] in 30 mL ALUMINUM OXIDE (UNII: LMI26O6933) (ALUMINUM OXIDE - UNII:LMI26O6933) ALUMINUM OXIDE 6 [hp_X] in 30 mL BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B) BRYONIA ALBA ROOT 6 [hp_X] in 30 mL SILYBUM MARIANUM SEED (UNII: U946SH95EE) (SILYBUM MARIANUM SEED - UNII:U946SH95EE) SILYBUM MARIANUM SEED 2 [hp_X] in 30 mL CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (CHELIDONIUM MAJUS - UNII:7E889U5RNN) CHELIDONIUM MAJUS 2 [hp_X] in 30 mL CHOLECALCIFEROL (UNII: 1C6V77QF41) (CHOLECALCIFEROL - UNII:1C6V77QF41) CHOLECALCIFEROL 2 [hp_X] in 30 mL COLLINSONIA (UNII: J9BTD5377V) (COLLINSONIA - UNII:J9BTD5377V) COLLINSONIA 2 [hp_X] in 30 mL SUS SCROFA COLON (UNII: 94J255A0UC) (SUS SCROFA COLON - UNII:94J255A0UC) SUS SCROFA COLON 12 [hp_X] in 30 mL POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D) POTASSIUM CARBONATE 6 [hp_X] in 30 mL SODIUM CARBONATE (UNII: 45P3261C7T) (CARBONATE ION - UNII:7UJQ5OPE7D) SODIUM CARBONATE 6 [hp_X] in 30 mL NIACIN (UNII: 2679MF687A) (NIACIN - UNII:2679MF687A) NIACIN 2 [hp_X] in 30 mL STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED 6 [hp_X] in 30 mL PANTOTHENIC ACID (UNII: 19F5HK2737) (PANTOTHENIC ACID - UNII:19F5HK2737) PANTOTHENIC ACID 2 [hp_X] in 30 mL SUS SCROFA RECTUM (UNII: QV1358E70N) (SUS SCROFA RECTUM - UNII:QV1358E70N) SUS SCROFA RECTUM 12 [hp_X] in 30 mL FRANGULA ALNUS BARK (UNII: S2D77IH61R) (FRANGULA ALNUS BARK - UNII:S2D77IH61R) FRANGULA ALNUS BARK 2 [hp_X] in 30 mL RHUBARB (UNII: G280W4MW6E) (RHUBARB - UNII:G280W4MW6E) RHUBARB 2 [hp_X] in 30 mL SKATOLE (UNII: 9W945B5H7R) (SKATOLE - UNII:9W945B5H7R) SKATOLE 10 [hp_X] in 30 mL TARAXACUM OFFICINALE (UNII: 39981FM375) (TARAXACUM OFFICINALE - UNII:39981FM375) TARAXACUM OFFICINALE 2 [hp_X] in 30 mL THIAMINE (UNII: X66NSO3N35) (THIAMINE ION - UNII:4ABT0J945J) THIAMINE 4 [hp_X] in 30 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) 9 mL in 30 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:17089-293-18 1 in 1 BOX 12/21/2018 1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 05/23/2006 Labeler - Guna spa (430538264) Establishment Name Address ID/FEI Business Operations Guna spa 338587646 manufacture(17089-293)