FDA.reportPublic FDA data

Hevert Detox Kidney

Manufacturer
Hevert Arzneimittel GmbH & Co KG | Hevert Arzneimittel GmbH & Co. KG
Effective date
2022-12-01
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 02:18:59

Label at a glance#

ProductHevert Detox Kidney
Active ingredientNitric Acid, Apis Mellifera, Atropa Belladonna, Lytta Vesicatoria, Juniper Berry, Solidago Virgaurea Flowering Top
Label structure10 sections

Indications and uses

For temporary relief of pain and burning sensation associated with frequent or urgent need to urinate. Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Dosage and administration

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.

Storage and handling

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.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active ingredientsPurpose
"X" indicates a homeopathic dilution. For more information visit: www.hevertusa.com
Acidum nitricum 6X*
Apis mellifica 3X*
Belladonna 6X*
Cantharis 4X*
Juniperus communis 3X*
Solidago virgaurea TM*

* pain relief in the urinary system

Uses

INDICATIONS & USAGE SECTION

For temporary relief of pain and burning sensation associated with frequent or urgent need to urinate.

Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Warnings

WARNINGS SECTION

For oral use only.

Blood in urine, fever, nausea, vomiting, pain in kidney area or acute urinary retention may be serious.

OTC - ASK DOCTOR SECTION

Consult a doctor promptly if any of these symptoms occur.

OTC - DO NOT USE SECTION

Do not use if

  • you are allergic to bee venom

OTC - STOP USE SECTION

Stop use and ask a doctor if symptoms persist for more than 5 days, worsen or new symptoms occur.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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.

Other information

STORAGE AND HANDLING SECTION

  • 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.

Inactive ingredients

INACTIVE INGREDIENT SECTION

60 % ethanol V/V, purified water

Questions?

OTC - QUESTIONS SECTION

1-855-387-6466

SPL UNCLASSIFIED SECTION

Distributed by:
Hevert Pharmaceuticals, LLC
Boulder, CO 80303

PRINCIPAL DISPLAY PANEL - 50 mL Bottle Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 54532-0032-5

HEVERT®
DETOX
KIDNEY

Homeopathic Medicine

For the kidneys and
urinary system

1.7 fl oz (50 ml)
60 % alcohol V/V
Oral drops

Made in Germany

hEVERT

PRINCIPAL DISPLAY PANEL - 50 mL Bottle Carton
PRINCIPAL DISPLAY PANEL - 50 mL Bottle Carton

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54532-0032-5Hevert Detox Kidney1 in 1 CARTONLIQUID16
54532-0032-5Hevert Detox Kidney50 mL in 1 BOTTLELIQUID506

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54532-0032HEVERT DETOX KIDNEY (NITRIC ACID, APIS MELLIFERA, ATROPA BELLADONNA, LYTTA VESICATORIA, JUNIPER BERRY, AND SOLIDAGO VIRGAUREA FLOWERING TOP) LIQUID [HEVERT ARZNEIMITTEL GMBH & CO KG]6Current NDC, Legacy NDC, 2 package rows20221220_cfad4864-7b02-4389-82f1-49669b651b48.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54532-003254532-0032-5

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
Nitric Acid411VRN1TV4ACTIB
Apis Mellifera7S82P3R43ZACTIB
Atropa BelladonnaWQZ3G9PF0HACTIB
Lytta Vesicatoria3Q034RO3BTACTIB
Juniper BerryO84B5194RLACTIB
Solidago Virgaurea Flowering Top5405K23S50ACTIB
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT

Source Document#

Source XML

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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
HEVERT DETOXARSENIC 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 OFFICINALEHevert Arzneimittel GmbH & Co KG78e83dc3-182e-4f4f-99df-f39b16953efb2022-12-15WarningsExact identifier
ndc (package): 54532-0032-5
ndc11 (package): 54532003205
Hevert Detox KidneyNITRIC ACID, APIS MELLIFERA, ATROPA BELLADONNA, LYTTA VESICATORIA, JUNIPER BERRY, AND SOLIDAGO VIRGAUREA FLOWERING TOPHevert Arzneimittel GmbH & Co KGcfad4864-7b02-4389-82f1-49669b651b482022-12-01WarningsExact identifier
ndc (package): 54532-0032-5
ndc (product): 54532-0032
ndc11 (package): 54532003205
spl id: 01fabd3b-07af-43df-9faf-5476d53a30a9
spl set id: cfad4864-7b02-4389-82f1-49669b651b48

Reported adverse events (FAERS/openFDA)#

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