Indications and uses
For temporary relief of symptoms of upset stomach and indigestion, such as: bloating abdominal fullness nausea constipation Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
For temporary relief of symptoms of upset stomach and indigestion, such as: bloating abdominal fullness nausea constipation Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Adults and children over 12 years of age: Take 20 drops in water 3 times daily. Consult a physician for use in children under 12 years of age.
Store at 68 to 77 °F. Tamper Evident: Do not use if tamper evident strip is broken or missing from base of bottle cap. To report serious adverse events, call 1-855-387-6466.
Drug Facts
| Active ingredients | Purpose |
|---|---|
| "X" indicates a homeopathic dilution. For more information visit: | |
| Eichhornia 1X | bloating constipation |
| Okoubaka 2X | nausea |
| Quassia amara TM | bloating |
| Taraxacum officinale 1X | bloating abdominal fullness |
For temporary relief of symptoms of upset stomach and indigestion, such as:
Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
For oral use only.
Stop use and ask a doctor if symptoms persist for more than 7 days, worsen or new symptoms occur.
If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
60 % ethanol V/V, purified water
1-855-387-6466
Distributed by:
Hevert Pharmaceuticals, LLC
Boulder, CO 80303
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 54532-0031-5 | Hevert Detox Intestinum | 50 mL in 1 BOTTLE | LIQUID | 50 | 4 | |
| 54532-0031-5 | Hevert Detox Intestinum | 1 in 1 CARTON | LIQUID | 1 | 4 |
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 54532-0031 | HEVERT DETOX INTESTINUM (EICHHORNIA CRASSIPES WHOLE, OKOUBAKA AUBREVILLEI BARK, QUASSIA AMARA WOOD, AND TARAXACUM OFFICINALE) LIQUID [HEVERT ARZNEIMITTEL GMBH & CO KG] | 4 | Current NDC, Legacy NDC, 2 package rows | 20221221_6c07bbb5-7770-4ab1-b336-00703e949fc9.zip |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 54532-0031 | 54532-0031-5 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| Eichhornia Crassipes Whole | 216V7S21BH | ACTIB |
| OKOUBAKA AUBREVILLEI BARK | MK2074187Z | ACTIB |
| QUASSIA AMARA WOOD | S5249Q85HW | ACTIB |
| TARAXACUM OFFICINALE | 39981FM375 | ACTIB |
| ALCOHOL | 3K9958V90M | IACT |
| WATER | 059QF0KO0R | IACT |
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 |
|---|---|---|---|---|---|---|
| HEVERT DETOX | ARSENIC TRIOXIDE, CLEMATIS RECTA FLOWERING TOP, CONIUM MACULATUM FLOWERING TOP, LACHESIS MUTA VENOM, MERCURIC IODIDE, PHYTOLACCA AMERICANA ROOT, TOXICODENDRON PUBESCENS SHOOT, SCROPHULARIA NODOSA LEAF WITH STEM, SULFUR, MILK THISTLE, CHELIDONIUM MAJUS ROOT, TARAXACUM OFFICINALE, NITRIC ACID, APIS MELLIFERA, ATROPA BELLADONNA, LYTTA VESICATORIA, JUNIPER BERRY, SOLIDAGO VIRGAUREA FLOWERING TOP, EICHHORNIA CRASSIPES WHOLE, OKOUBAKA AUBREVILLEI BARK, QUASSIA AMARA WOOD, AND TARAXACUM OFFICINALE | Hevert Arzneimittel GmbH & Co KG | 78e83dc3-182e-4f4f-99df-f39b16953efb | 2022-12-15 | Warnings | 54532-0031-5 54532003105 |
| Hevert Detox Intestinum | EICHHORNIA CRASSIPES WHOLE, OKOUBAKA AUBREVILLEI BARK, QUASSIA AMARA WOOD, AND TARAXACUM OFFICINALE | Hevert Arzneimittel GmbH & Co KG | 6c07bbb5-7770-4ab1-b336-00703e949fc9 | 2022-11-30 | Warnings | 54532-0031-5 54532-0031 54532003105 5fd4ef4b-cf67-4828-8492-266a585109a6 6c07bbb5-7770-4ab1-b336-00703e949fc9 |
Adverse event summaries are temporarily unavailable. Other product information remains available.