FDA.reportPublic FDA data

Bryonia Eucalyptus

Manufacturer
Uriel Pharmacy Inc.
Effective date
2024-12-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:29:20

Label at a glance#

ProductBryonia Eucalyptus
Active ingredientACONITUM NAPELLUS, EUPATORIUM PERFOLIATUM FLOWERING TOP, FERROSOFERRIC PHOSPHATE, BRYONIA ALBA ROOT, EUCALYPTUS GUM, QUILLAJA SAPONARIA BARK
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Dissolve pellets under the tongue 3-4 times daily. Ages 12 and older: 10 pellets. Ages 2-11: 5 pellets. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Aconitum (Monkshood) 3X, Bryonia (White bryony) 3X, China (Peruvian bark) 3X, Eupatorium cann. (Hemp agrimony) 3X, Eucalyptus 3X, Vivianite (Nat. ferrous phosphate) 7X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Organic sucrose, Lactose

OTC - PURPOSE SECTION

Use: Temporary relief of flu symptoms.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. Do not use if allergic to any ingredient. Contains traces of lactose. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
shopuriel.com Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bryonia Eucalyptus PelletsBryonia Eucalyptus Pellets

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-2136-2Bryonia Eucalyptus1350 in 1 BOTTLE, GLASSPELLET13502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-2136BRYONIA EUCALYPTUS PELLET [URIEL PHARMACY INC.]2Legacy NDC, 1 package rows20241207_97b65c02-1229-07db-e053-2a95a90ac4fe.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-213648951-2136-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
ACONITUM NAPELLUSU0NQ8555JDACTIB
EUPATORIUM PERFOLIATUM FLOWERING TOP1W0775VX6EACTIB
FERROSOFERRIC PHOSPHATE91GQH8I5F7ACTIB
SUCROSEC151H8M554IACT
BRYONIA ALBA ROOTT7J046YI2BACTIB
EUCALYPTUS GUM72T9EZC2VXACTIB
LACTOSE, UNSPECIFIED FORMJ2B2A4N98GIACT
QUILLAJA SAPONARIA BARK8N0K3807ZWACTIB

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
287730fb-400d-aeb0-e063-6394a90ac69197b65c02-1229-07db-e053-2a95a90ac4fe2024-12-04WarningsExact identifier
spl id: 287730fb-400d-aeb0-e063-6394a90ac691
spl set id: 97b65c02-1229-07db-e053-2a95a90ac4fe

Reported adverse events (FAERS/openFDA)#

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