FDA.reportPublic FDA data

BioE Joints

Manufacturer
BioEnergetics, Inc.
Effective date
2018-03-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:00:33

Label at a glance#

ProductBioE Joints
Active ingredientCOLCHICUM AUTUMNALE FLOWER, FORMICA RUFA, LACHESIS MUTA VENOM, RHODODENDRON TOMENTOSUM LEAFY TWIG, LYCOPODIUM CLAVATUM SPORE, RHODODENDRON AUREUM LEAF, TOXICODENDRON RADICANS LEAF, ALLYLTHIOUREA, URTICA URENS
Label structure6 sections

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Colchicum 6x, Formica rufa 6x, Lachesis mutus 30x, Ledum palustre 9x, Lycopodium 6x, Rhododendron 8x, Rhus tox 6x, Thiosinaminum 6x, Urtica urens 6x

Purpose

OTC - PURPOSE SECTION

Inactive ingredients:

INACTIVE INGREDIENT SECTION

alcohol 20%, purified water.

INDICATIONS & USAGE SECTION

Swollen, painful joints. Symptoms of arthritis, bursitis, rheumatism.

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

Dosage:

DOSAGE & ADMINISTRATION SECTION

In general, 10 drops under the tongue 3 times daily. In acute conditions, 10 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

BioE JointsBioE Joints

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57293-442557293-4425-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
COLCHICUM AUTUMNALE FLOWER097FL89535ACTIB
FORMICA RUFA55H0W83JO5ACTIB
LACHESIS MUTA VENOMVSW71SS07IACTIB
RHODODENDRON TOMENTOSUM LEAFY TWIG877L01IZ0PACTIB
LYCOPODIUM CLAVATUM SPOREC88X29Y479ACTIB
RHODODENDRON AUREUM LEAFIV92NQJ73UACTIB
TOXICODENDRON RADICANS LEAFCDH3461U7LACTIB
ALLYLTHIOUREA706IDJ14B7ACTIB
URTICA URENSIHN2NQ5OF9ACTIB

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
d3507fbb-744d-e1da-e053-2a95a90a78a74f522d15-1885-41c5-83c0-edbe6f03b9232021-12-16WarningsExact identifier
spl set id: 4f522d15-1885-41c5-83c0-edbe6f03b923

Reported adverse events (FAERS/openFDA)#

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