BHI Diarrhea

ALOE, ACTIVATED CHARCOAL, CITRULLUS COLOCYNTHIS FRUIT PULP, CUPRIC ACETATE, FERRUM PHOSPHORICUM, PODOPHYLLUM, POTENTILLA ERECTA ROOT, AND VERATRUM ALBUM ROOT ORAL HUMAN OTC DRUG

BHI Diarrhea is an FDA drug label for the active ingredient ALOE, ACTIVATED CHARCOAL, CITRULLUS COLOCYNTHIS FRUIT PULP, CUPRIC ACETATE, FERRUM PHOSPHORICUM, PODOPHYLLUM, POTENTILLA ERECTA ROOT, AND VERATRUM ALBUM ROOT manufactured by MediNatura Inc administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20230821.

Generic name
ALOE, ACTIVATED CHARCOAL, CITRULLUS COLOCYNTHIS FRUIT PULP, CUPRIC ACETATE, FERRUM PHOSPHORICUM, PODOPHYLLUM, POTENTILLA ERECTA ROOT, AND VERATRUM ALBUM ROOT
Manufacturer
MediNatura Inc
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
62795-1021
Application
N/A
Label effective
20230821

About this product

BHI Diarrhea is an FDA-registered drug product whose active ingredient is ALOE, ACTIVATED CHARCOAL, CITRULLUS COLOCYNTHIS FRUIT PULP, CUPRIC ACETATE, FERRUM PHOSPHORICUM, PODOPHYLLUM, POTENTILLA ERECTA ROOT, AND VERATRUM ALBUM ROOT. It is labelled by MediNatura Inc taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 62795-1021, label effective 20230821. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing ALOE, ACTIVATED CHARCOAL, CITRULLUS COLOCYNTHIS FRUIT PULP, CUPRIC ACETATE, FERRUM PHOSPHORICUM, PODOPHYLLUM, POTENTILLA ERECTA ROOT, AND VERATRUM ALBUM ROOT are most often described in connection with: temporary relief, mild diarrhea, stomach ache. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

ACTIVE INGREDIENTS Each tablet contains: *Aloe socotrina 4X, *Carbo vegetabilis 12X *Colocynthis 6X, Cuprum aceticum 6X, Ferrum phosphoricum 10X, *Podophyllum peltatum 6X, *Tormentilla 4X, *Veratrum album 5X 37.5 mg each. *Natural Ingredients

Indications & Usage

USES For the temporary relief of mild diarrhea, travelers’ diarrhea, stomach ache

Dosage & Administration

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 .

Warnings

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.

Frequently asked questions

What is BHI Diarrhea used for?
USES For the temporary relief of mild diarrhea, travelers’ diarrhea, stomach ache

Who makes BHI Diarrhea?
MediNatura Inc is the labeler of record for BHI Diarrhea.

What form does BHI Diarrhea come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is BHI Diarrhea prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Has BHI Diarrhea been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.