FDA.reportPublic FDA data

Inflammation Drops

Manufacturer
BioEnergetics, Inc.
Effective date
2018-03-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:00:37

Label at a glance#

ProductInflammation
Active ingredientAPIS MELLIFERA, ARNICA MONTANA, ATROPA BELLADONNA, CHLORINE, ECHINACEA ANGUSTIFOLIA, FERRIC CHLORIDE HEXAHYDRATE, CALCIUM SULFIDE, MERCURIUS SOLUBILIS, PHYTOLACCA AMERICANA ROOT, TOXICODENDRON PUBESCENS LEAF, ALCOHOL, X-RAY EXPOSED (1000 RAD)
Label structure6 sections

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Apix mel 6x, Arnica montana 6x, Belladonna 12x, Chlorium 12x, Echinacea angust 4x, Ferrum mur 12x, Hepar sulf 12x, Merc sol 12x, Phytolacca 6x, Rhus tox 6x, X-Ray 20C

Purpose

OTC - PURPOSE SECTION

Inactive ingredients:

INACTIVE INGREDIENT SECTION

alcohol 20%, purified water.

INDICATIONS & USAGE SECTION

Recommended for inflammation and fever. Symptoms include heat, pain, redness and swelling.

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 sysmptoms 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

InflammationInflammation

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57293-441557293-4415-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
APIS MELLIFERA7S82P3R43ZACTIB
ARNICA MONTANAO80TY208ZWACTIB
ATROPA BELLADONNAWQZ3G9PF0HACTIB
CHLORINE4R7X1O2820ACTIB
ECHINACEA ANGUSTIFOLIAVB06AV5US8ACTIB
FERRIC CHLORIDE HEXAHYDRATE0I2XIN602UACTIM
CALCIUM SULFIDE1MBW07J51QACTIB
MERCURIUS SOLUBILIS324Y4038G2ACTIB
PHYTOLACCA AMERICANA ROOT11E6VI8VEGACTIB
TOXICODENDRON PUBESCENS LEAF6IO182RP7AACTIB
ALCOHOL, X-RAY EXPOSED (1000 RAD)6PRJ93602PACTIB

Source Document#

Source XML · Source PDF

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
d350b779-0206-7476-e053-2a95a90a9cb8c16dacc3-3f8d-452e-b52b-51df6e69a8302021-12-16WarningsExact identifier
spl set id: c16dacc3-3f8d-452e-b52b-51df6e69a830

Reported adverse events (FAERS/openFDA)#

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