Indications and uses
For the temporary relief of minor constipation, bowel irregularity, bloating
BHI Constipation Tablet
- Manufacturer
- MediNatura Inc | MediNatura
- Effective date
- 2022-07-07
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- full-release
- Hydrated at
- 2026-06-01 02:17:40
Label at a glance#
ProductBHI Constipation
Active ingredientDIOSCOREA VILLOSA TUBER, SODIUM CHLORIDE, STRYCHNOS NUX-VOMICA SEED
Label structure8 sections
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: Take1-2 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
Each tablet contains: *Dioscorea villosa 4X, Natrum muriaticum 200X, *Nux vomica 8X 100 mg each.
*Natural Ingredients
INACTIVE INGREDIENTS
Inactive Ingredients:Dextrose, Magnesium Stearate, Maltodextrin
.
PURPOSE
Constipation Relief Tablets
Relieves:
• Constipation
• Bowel Irregularity
• Bloating
USES
For the temporary relief of minor constipation, bowel irregularity, bloating
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: Take1-2 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
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 known sensitivity to BHI Constipation or any of its ingredients exists.
KEEP OUT OF REACH OF CHILDREN
Keep out of reach of children.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 62795-1005-3 | BHI Constipation | 100 in 1 BOTTLE | TABLET | 100 | 4 | |
| 62795-1005-3 | BHI Constipation | 1 in 1 CARTON | TABLET | 1 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 62795-1005 | BHI CONSTIPATION (DIOSCOREA VILLOSA TUBER, SODIUM CHLORIDE, AND STRYCHNOS NUX-VOMICA SEED) TABLET [MEDINATURA INC] | 4 | Current NDC, Legacy NDC, 2 package rows | 20220708_0365b75b-fee4-4c1d-89ab-c692bdd73f75.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 62795-1005-2 | EA - Each | 62795-1005 | c5ce4aaa-8597-43e7-a4e6-58e5db9f6bda | 1 | 2015-10-02 |
| 62795-1005-3 | EA - Each | 62795-1005 | 5027f2b2-1c2b-4b0e-b8d8-986fec1790c5 | 1 | 2023-06-06 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| DIOSCOREA VILLOSA TUBER | ACTIVE INGREDIENT | IWY3IWX2G8 | 1 | |
| SODIUM CHLORIDE | ACTIVE INGREDIENT | 451W47IQ8X | 1 | |
| STRYCHNOS NUX-VOMICA SEED | ACTIVE INGREDIENT | 269XH13919 | 1 | |
| CHLORIDE ION | ACTIVE MOIETY | Q32ZN48698 | 1 | |
| DIOSCOREA VILLOSA ROOT | ACTIVE MOIETY | IWY3IWX2G8 | 1 | |
| STRYCHNOS NUX-VOMICA SEED | ACTIVE MOIETY | 269XH13919 | 1 | |
| LACTOSE | INACTIVE INGREDIENT | J2B2A4N98G | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | 1 |
Products#
Every source-derived product name is available through these pages.
- BHI Constipation
- DIOSCOREA VILLOSA TUBER, SODIUM CHLORIDE, and STRYCHNOS NUX-VOMICA SEED
- DIOSCOREA VILLOSA TUBER
- DIOSCOREA VILLOSA ROOT
- SODIUM CHLORIDE
- CHLORIDE ION
- STRYCHNOS NUX-VOMICA SEED
- MAGNESIUM STEARATE
- DEXTROSE
- MALTODEXTRIN
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 62795-1005 | 62795-1005-3 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| DIOSCOREA VILLOSA TUBER | IWY3IWX2G8 | ACTIB |
| SODIUM CHLORIDE | 451W47IQ8X | ACTIB |
| STRYCHNOS NUX-VOMICA SEED | 269XH13919 | ACTIB |
| MAGNESIUM STEARATE | 70097M6I30 | IACT |
| DEXTROSE | IY9XDZ35W2 | IACT |
| MALTODEXTRIN | 7CVR7L4A2D | IACT |
Source Document#
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.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| MAGNESIUM STEARATE | MAGNESIUM STEARATE | 70097M6I30 | TABLET / ORAL | 980 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | TABLET / ORAL | 2500 mg | ||
| MAGNESIUM STEARATE | MAGNESIUM STEARATE | 70097M6I30 | TABLET / ORAL | 980 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | TABLET / ORAL | 2500 mg |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| BHI Constipation | DIOSCOREA VILLOSA TUBER, SODIUM CHLORIDE, AND STRYCHNOS NUX-VOMICA SEED | MediNatura Inc | 0365b75b-fee4-4c1d-89ab-c692bdd73f75 | 2022-07-07 | Warnings | 62795-1005-3 62795-1005 62795100503 25f16472-f472-48be-a1f9-d5741bcf2686 0365b75b-fee4-4c1d-89ab-c692bdd73f75 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.