FDA.reportPublic FDA data

Body Mend

Manufacturer
BioEnergetics, Inc.
Effective date
2019-12-09
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:50:40

Label at a glance#

ProductBody Mend
Active ingredientARNICA MONTANA, ATROPA BELLADONNA, BELLIS PERENNIS, CALENDULA OFFICINALIS FLOWERING TOP, ECHINACEA PURPUREA, EUPATORIUM PERFOLIATUM FLOWERING TOP, HAMAMELIS VIRGINIANA LEAF, HYPERICUM PERFORATUM, STRYCHNOS NUX-VOMICA SEED, RUTA GRAVEOLENS FLOWERING TOP, DELPHINIUM STAPHISAGRIA SEED, COMFREY ROOT, ALLYLTHIOUREA, VERATRUM ALBUM ROOT
Label structure6 sections

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Arnica mont 6x, Belladonna 12x, Bellis perennis 6x, Calendula off 4x, Echinacea purp 5x, Eupatorium perf 9x, Hamamelis 5x, Hypericum perf 6x, Nux vomica 12x, Ruta grav 6x, Staphysagria 9x, Symphytum off 9x, Thiosinaminum 6x, veratrum alb 4C.

Purpose

OTC - PURPOSE SECTION

Inactive ingredients:

INACTIVE INGREDIENT SECTION

alcohol 20%, purified water.

INDICATIONS & USAGE SECTION

To assist in recovery from minor injuries such as sprains, strains, cuts & bruises.

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

Body MendBody Mend

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
57293-440957293-4409-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
ARNICA MONTANAO80TY208ZWACTIB
ATROPA BELLADONNAWQZ3G9PF0HACTIB
BELLIS PERENNIS2HU33I03UYACTIB
CALENDULA OFFICINALIS FLOWERING TOP18E7415PXQACTIB
ECHINACEA PURPUREAQI7G114Y98ACTIB
EUPATORIUM PERFOLIATUM FLOWERING TOP1W0775VX6EACTIB
HAMAMELIS VIRGINIANA LEAFT07U1161SVACTIB
HYPERICUM PERFORATUMXK4IUX8MNBACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
RUTA GRAVEOLENS FLOWERING TOPN94C2U587SACTIB
DELPHINIUM STAPHISAGRIA SEED00543AP1JVACTIB
COMFREY ROOTM9VVZ08EKQACTIB
ALLYLTHIOUREA706IDJ14B7ACTIB
VERATRUM ALBUM ROOTQNS6W5US1ZACTIB

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
d3500600-1dcb-7279-e053-2995a90a1c08d90693e2-6455-465e-aa09-07c083aff15e2021-12-16WarningsExact identifier
spl set id: d90693e2-6455-465e-aa09-07c083aff15e

Reported adverse events (FAERS/openFDA)#

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