BHI Diarrhea Tablet

Manufacturer
MediNatura Inc
Effective date
2023-08-21
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:22:04

Label at a glance#

ProductBHI Diarrhea
Active ingredientALOE, ACTIVATED CHARCOAL, CITRULLUS COLOCYNTHIS FRUIT PULP, CUPRIC ACETATE, FERRUM PHOSPHORICUM, PODOPHYLLUM, POTENTILLA ERECTA ROOT, VERATRUM ALBUM ROOT
Label structure8 sections

Indications and uses

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

Dosage and administration

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 .

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

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

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Inactive Ingredients: **Dextrose, ** Lactose, Magnesium Stearate, **Maltodextrin
**contains one or more of these ingredients.

PURPOSE

OTC - PURPOSE SECTION

Diarrhea Relief Tablets

Relieves:

• Diarrhea

• Travelers’ Diarrhea

• Stomach Ache

USES

INDICATIONS & USAGE SECTION

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

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 SECTION

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.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BHI Diarrhea Tablet.jpgBHI Diarrhea Tablet.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62795-1021-2BHI Diarrhea100 in 1 BOTTLETABLET1005
62795-1021-3BHI Diarrhea1 in 1 CARTONTABLET15
62795-1021-3BHI Diarrhea100 in 1 BOTTLETABLET1005
62795-1021-4BHI Diarrhea60 in 1 BOTTLETABLET605

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62795-1021BHI DIARRHEA (ALOE, ACTIVATED CHARCOAL, CITRULLUS COLOCYNTHIS FRUIT PULP, CUPRIC ACETATE, FERRUM PHOSPHORICUM, PODOPHYLLUM, POTENTILLA ERECTA ROOT, AND VERATRUM ALBUM ROOT) TABLET [MEDINATURA INC]5Current NDC, Legacy NDC, 4 package rows20230822_6e58f888-429a-4497-8fe5-4ccd829fcb28.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
62795-1021-2EA - Each62795-1021423f8df4-b2da-4d90-9fb8-2539d3ed2ec712015-11-12

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ACTIVATED CHARCOALACTIVE INGREDIENT2P3VWU3H101
ALOEACTIVE INGREDIENTV5VD430YW91
CITRULLUS COLOCYNTHIS FRUIT PULPACTIVE INGREDIENT23H32AOH171
CUPRIC ACETATEACTIVE INGREDIENT39M11XPH031
FERRUM PHOSPHORICUMACTIVE INGREDIENT91GQH8I5F71
PODOPHYLLUMACTIVE INGREDIENT2S713A4VP31
POTENTILLA ERECTA ROOTACTIVE INGREDIENTBI896CKT6B1
VERATRUM ALBUM ROOTACTIVE INGREDIENTQNS6W5US1Z1
ACTIVATED CHARCOALACTIVE MOIETY2P3VWU3H101
ALOEACTIVE MOIETYV5VD430YW91
CITRULLUS COLOCYNTHIS FRUIT PULPACTIVE MOIETY23H32AOH171
CUPRIC CATIONACTIVE MOIETY8CBV67279L1
FERROSOFERRIC PHOSPHATEACTIVE MOIETY91GQH8I5F71
PODOPHYLLUMACTIVE MOIETY2S713A4VP31
POTENTILLA ERECTA ROOTACTIVE MOIETYBI896CKT6B1
VERATRUM ALBUM ROOTACTIVE MOIETYQNS6W5US1Z1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98G1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I301

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62795-102162795-1021-3, 62795-1021-2, 62795-1021-4

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Source Document#

Source XML · Source PDF

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 8 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET / ORAL2500 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET / ORAL2500 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET / ORAL2500 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET / ORAL2500 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
BHI DiarrheaALOE, ACTIVATED CHARCOAL, CITRULLUS COLOCYNTHIS FRUIT PULP, CUPRIC ACETATE, FERRUM PHOSPHORICUM, PODOPHYLLUM, POTENTILLA ERECTA ROOT, AND VERATRUM ALBUM ROOTMediNatura Inc6e58f888-429a-4497-8fe5-4ccd829fcb282023-08-21WarningsExact identifier
ndc (package): 62795-1021-2
ndc (package): 62795-1021-4
ndc (package): 62795-1021-3
ndc (product): 62795-1021
ndc11 (package): 62795102102
ndc11 (package): 62795102103
ndc11 (package): 62795102104
spl id: 23d3e637-436b-4ceb-9d95-71446bf9b145
spl set id: 6e58f888-429a-4497-8fe5-4ccd829fcb28

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.