NDC 17089-470

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 -

GUNA BOWEL PLUS is a Oral Solution/ Drops in the Human Otc Drug category. It is labeled and distributed by Guna Spa. The primary component is Aloe; Aluminum Oxide; Bryonia Alba Root; Silybum Marianum Seed; Chelidonium Majus; Activated Charcoal; Collinsonia; Sus Scrofa Pancreas; Potassium Carbonate; Sodium Carbonate; Lycopodium Clavatum Spore; Strychnos Nux-vomica Seed; Frangula Alnus Bark; Rhubarb; Skatole; Taraxacum Officinale; Thiamine.

Product ID17089-470_b3aa6401-9af7-b0d5-e053-2995a90a10ef
NDC17089-470
Product TypeHuman Otc Drug
Proprietary NameGUNA BOWEL PLUS
Generic NameActivated 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 -
Dosage FormSolution/ Drops
Route of AdministrationORAL
Marketing Start Date2021-01-17
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameGuna spa
Substance NameALOE; ALUMINUM OXIDE; BRYONIA ALBA ROOT; SILYBUM MARIANUM SEED; CHELIDONIUM MAJUS; ACTIVATED CHARCOAL; COLLINSONIA; SUS SCROFA PANCREAS; POTASSIUM CARBONATE; SODIUM CARBONATE; LYCOPODIUM CLAVATUM SPORE; STRYCHNOS NUX-VOMICA SEED; FRANGULA ALNUS BARK; RHUBARB; SKATOLE; TARAXACUM OFFICINALE; THIAMINE
Active Ingredient Strength4 [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
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 17089-470-18

1 BOTTLE, DROPPER in 1 BOX (17089-470-18) > 30 mL in 1 BOTTLE, DROPPER
Marketing Start Date2021-01-17
NDC Exclude FlagN
Sample Package?N

Drug Details


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