FDA.reportPublic FDA data

Lymphohepat

Manufacturer
BioEnergetics, Inc.
Effective date
2019-12-09
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:50:39

Label at a glance#

ProductLymphohepat
Active ingredientARSENIC TRIOXIDE, CALENDULA OFFICINALIS FLOWERING TOP, MILK THISTLE, CHELIDONIUM MAJUS, MARSDENIA CONDURANGO BARK, ECHINACEA, UNSPECIFIED, GOLDENSEAL, VERONICASTRUM VIRGINICUM ROOT, LYCOPODIUM CLAVATUM SPORE, PHYTOLACCA AMERICANA ROOT, SANGUINARIA CANADENSIS ROOT, TARAXACUM PALUSTRE ROOT
Label structure6 sections

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Arsenicum alb 12x,  Calendula off 4x, Cardus mar 6x, Chelidonium 4x, Condurango 6x, Echinacea 4x, Hydrastis 9x, Leptandra 6x, Lycopodium 6x,  Phytolacca 6x, Sanguinaria 6x, Taraxacum 6x

Purpose

OTC - PURPOSE SECTION

Inactive ingredients:

INACTIVE INGREDIENT SECTION

alcohol 20%, purified water.

INDICATIONS & USAGE SECTION

To assist the body's natural cleansing process of drainage. Symptoms include itching, mucous, feeling of sluggishness.

These uses are based on traditional homeopathic practice. They have not been evauated by the FDA.

Dosage:

DOSAGE & ADMINISTRATION SECTION

In general, 20 drops under the tongue 3 times daily. In acute conditions, 20 drops every 15 minutes.  Children, one half the above dosage. For children 2 years and under, and for people nursing a baby or pregnant, seek the advice of a health professional before use.

WARNINGS SECTION

DO NOT USE

OTC - DO NOT USE SECTION

IF BioE IMPRINTED SEAL ON NECK IS BROKEN

OTC - STOP USE SECTION

If symptoms worsen or persist for more than 7 days, consult a physician.

Keep out of the reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LymphohepatLymphohepat

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57293-441957293-4419-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
ARSENIC TRIOXIDES7V92P67HOACTIB
CALENDULA OFFICINALIS FLOWERING TOP18E7415PXQACTIB
MILK THISTLEU946SH95EEACTIB
CHELIDONIUM MAJUS7E889U5RNNACTIB
MARSDENIA CONDURANGO BARKR23QIR6YBAACTIB
ECHINACEA, UNSPECIFIED4N9P6CC1DXACTIB
GOLDENSEALZW3Z11D0JVACTIB
VERONICASTRUM VIRGINICUM ROOTM2O62YTN42ACTIB
LYCOPODIUM CLAVATUM SPOREC88X29Y479ACTIB
PHYTOLACCA AMERICANA ROOT11E6VI8VEGACTIB
SANGUINARIA CANADENSIS ROOTN9288CD508ACTIB
TARAXACUM PALUSTRE ROOTGCZ4W7077CACTIB

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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d34facdc-060e-bc2a-e053-2995a90a3d13cdf6c0e6-6f22-4792-90b5-2035e3b8c2ef2021-12-16WarningsExact identifier
spl set id: cdf6c0e6-6f22-4792-90b5-2035e3b8c2ef

Reported adverse events (FAERS/openFDA)#

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