Label: BHI DIARRHEA- aloe, activated charcoal, citrullus colocynthis fruit pulp, cupric acetate, ferrum phosphoricum, podophyllum, potentilla erecta root, and veratrum album root tablet
- NDC Code(s): 62795-1021-2, 62795-1021-3, 62795-1021-4
- Packager: MediNatura Inc
- 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 August 21, 2023
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
- INACTIVE INGREDIENTS
- PURPOSE
- USES
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DIRECTIONS
At first sign of symptoms: Adults and children 4 years and older:
1 tablet every 1/2 to 1 hour until symptoms lessen, then continue with standard dosage.
Standard dosage: Adults and children 4 years and older:
Take 1-2 tablets every 4 to 6 hours. Do not exceed 12 tablets in 24 hours
For children under 4, consult your health professional.
Allow tablets to dissolve completely in the mouth, do not swallow
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WARNINGS
If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If symptoms persist or worsen, a health professional should be consulted. Do not use if you have bloody or black stool. Stop use and ask a doctor if symptoms get worse or diarrhea lasts more than 2 days, have a fever, or have mucus in the stool. Drink plenty of clear fluids to help prevent dehydration caused by diarrhea. Do not use if known sensitivity to BHI Diarrhea or any of its ingredients exists.
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- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BHI DIARRHEA
aloe, activated charcoal, citrullus colocynthis fruit pulp, cupric acetate, ferrum phosphoricum, podophyllum, potentilla erecta root, and veratrum album root tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62795-1021 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALOE (UNII: V5VD430YW9) (ALOE - UNII:V5VD430YW9) ALOE 4 [hp_X] ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10) ACTIVATED CHARCOAL 12 [hp_X] CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17) (CITRULLUS COLOCYNTHIS FRUIT PULP - UNII:23H32AOH17) CITRULLUS COLOCYNTHIS FRUIT PULP 6 [hp_X] CUPRIC ACETATE (UNII: 39M11XPH03) (CUPRIC CATION - UNII:8CBV67279L) CUPRIC ACETATE 6 [hp_X] FERRUM PHOSPHORICUM (UNII: 91GQH8I5F7) (FERROSOFERRIC PHOSPHATE - UNII:91GQH8I5F7) FERRUM PHOSPHORICUM 10 [hp_X] PODOPHYLLUM (UNII: 2S713A4VP3) (PODOPHYLLUM - UNII:2S713A4VP3) PODOPHYLLUM 6 [hp_X] POTENTILLA ERECTA ROOT (UNII: BI896CKT6B) (POTENTILLA ERECTA ROOT - UNII:BI896CKT6B) POTENTILLA ERECTA ROOT 4 [hp_X] VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z) (VERATRUM ALBUM ROOT - UNII:QNS6W5US1Z) VERATRUM ALBUM ROOT 5 [hp_X] Inactive Ingredients Ingredient Name Strength LACTOSE (UNII: J2B2A4N98G) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) DEXTROSE (UNII: IY9XDZ35W2) Product Characteristics Color white Score no score Shape ROUND Size 9mm Flavor Imprint Code Leafman Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62795-1021-3 1 in 1 CARTON 08/30/2014 1 100 in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:62795-1021-2 100 in 1 BOTTLE; Type 0: Not a Combination Product 04/11/2022 3 NDC:62795-1021-4 60 in 1 BOTTLE; Type 0: Not a Combination Product 08/21/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/30/2014 Labeler - MediNatura Inc (079324099) Establishment Name Address ID/FEI Business Operations MediNatura Inc 102783016 manufacture(62795-1021)
