FDA.reportPublic FDA data

Allergy Drops

Manufacturer
BioEnergetics, Inc.
Effective date
2019-12-09
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:50:17

Label at a glance#

ProductAllergy
Active ingredientONION, AMBROSIA ARTEMISIIFOLIA, APIS MELLIFERA, EUPHRASIA STRICTA, GELSEMIUM SEMPERVIRENS ROOT, CANNABIS SATIVA POLLEN, SCHOENOCAULON OFFICINALE SEED, LOBARIA PULMONARIA
Label structure6 sections

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Allium cepa HPUS 6x

Ambrosia artem HPUS 6x

Apis mel HPUS 6x

Euphrasia off HPUS 6x

Gelsemium semp HPUS 6x

Mixed Grass Pollens 30C

Sabadilla HPUS 6x

Sticta pulmonaria HPUS 6x

Purpose

OTC - PURPOSE SECTION

Inactive ingredients:

INACTIVE INGREDIENT SECTION

alcohol 20%, purified water.

INDICATIONS & USAGE SECTION

For allergy sysmptoms, including watering, itchy eyes, runny nose, sneezing, swollen eye lids, itchy nostrils.

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

Allergy DropsAllergy Drops

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57293-440657293-4406-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
ONION492225Q21HACTIB
AMBROSIA ARTEMISIIFOLIA9W34L2CQ9AACTIB
APIS MELLIFERA7S82P3R43ZACTIB
EUPHRASIA STRICTAC9642I91WLACTIB
GELSEMIUM SEMPERVIRENS ROOT639KR60Q1QACTIB
CANNABIS SATIVA POLLEN87TOI623SHACTIB
SCHOENOCAULON OFFICINALE SEED6NAF1689IOACTIB
LOBARIA PULMONARIAD1YM0P5Z2TACTIB

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
d34fc1fa-8ca2-bbf6-e053-2995a90a21614b32f3c1-2b40-4435-a5ff-879d61fff5fb2021-12-16WarningsExact identifier
spl set id: 4b32f3c1-2b40-4435-a5ff-879d61fff5fb

Reported adverse events (FAERS/openFDA)#

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