Bryonia Eucalyptus Flu Relief

Manufacturer: Uriel Pharmacy Inc
Effective date: 2009-12-03
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:02:54

Label at a glance#

ProductBryonia Eucalyptus Flu Relief

Active ingredientACONITUM NAPELLUS ROOT, BRYONIA CRETICA SUBSP. DIOICA ROOT, EUPATORIUM CANNABINUM WHOLE FLOWERING, CINCHONA OFFICINALIS BARK, EUCALYPTUS GLOBULUS LEAF

Label structure10 sections

Contacts and useful links#

PhoneLabel contact866 642-2858

Websitewww.urielpharmacy.com

www.urielpharmacy.com

Label contents#

Full prescribing information#

Purpose

OTC - PURPOSE SECTION

Uses: Temporarily relieves symptoms of influenza (flu).

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION

Directions: Dissolve under tongue every hour as needed, decreasing to 4 times daily as symptoms improve. Age 12 and older: 10 pellets. Ages 2-11: 5 pellets. Under age 2: ask a doctor.

OTC-Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Aconitum e tub. 3X, Bryonia e rad. 3X, Eupatorium cann. ex herba 3X, China e cort. 3X, Eucalyptus e fol. 3X, all HPUS.

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Inactive Ingredient: Sucrose, Vivianite 7X.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

Do not use section

OTC - DO NOT USE SECTION

Warnings: Do not use if allergic to any ingredient. Do not use if safety seal is broken or missing.

Ask doctor section

OTC - ASK DOCTOR SECTION

Consult a doctor if symptoms are serious or persist for 3 days, if you are diabetic or intolerant of sugar.

Pregnancy or breast feeding section

OTC - PREGNANCY OR BREAST FEEDING SECTION

If you are pregnant or nursing, consult a doctor before use.

Questions section

OTC - QUESTIONS SECTION

Questions? Uriel Pharmacy

866 642-2858 East Troy, WI 53120

www.urielpharmacy.com

NDC 48951-2084-2

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bryonia Eucalyptus

Flu Relief

Homeopathic Pellets

net wt. 1 oz.

bryonia eucalyptus pellets bottle label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
48951-2084-2	2020-01-31	C162847	48780-1	9d75b9d0-d3ba-f424-e053-dadaa90a57ce	Bryonia Eucalyptus Flu Relief Pellets - 1 oz.

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-2084-2	Bryonia Eucalyptus Flu Relief	1350 in 1 BOTTLE, GLASS	PELLET	1350		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-2084	BRYONIA EUCALYPTUS FLU RELIEF (ACONITUM NAPELLUS ROOT BRYONIA CRETICA SUBSP. DIOICA ROOT EUPATORIUM CANNABINUM WHOLE FLOWERING CINCHONA OFFICINALIS BARK EUCALYPTUS GLOBULUS LEAF) PELLET [URIEL PHARMACY INC]	1	Legacy NDC, 1 package rows	20110113_9a61ae10-e04d-11de-8a39-0800200c9a66.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
ACONITUM NAPELLUS ROOT	ACTIVE INGREDIENT	KPD2N7348X	1
BRYONIA CRETICA SUBSP. DIOICA ROOT	ACTIVE INGREDIENT	53UB5FH7CX	1
CINCHONA OFFICINALIS BARK	ACTIVE INGREDIENT	S003A158SB	1
EUCALYPTUS GLOBULUS LEAF	ACTIVE INGREDIENT	S546YLW6E6	1
EUPATORIUM CANNABINUM WHOLE FLOWERING	ACTIVE INGREDIENT	A5296YC7FS	1
ACONITUM NAPELLUS ROOT	ACTIVE MOIETY	KPD2N7348X	1
BRYONIA CRETICA SUBSP. DIOICA ROOT	ACTIVE MOIETY	53UB5FH7CX	1
CINCHONA OFFICINALIS BARK	ACTIVE MOIETY	S003A158SB	1
EUCALYPTUS GLOBULUS LEAF	ACTIVE MOIETY	S546YLW6E6	1
EUPATORIUM CANNABINUM WHOLE FLOWERING	ACTIVE MOIETY	A5296YC7FS	1
SUCROSE	INACTIVE INGREDIENT	C151H8M554	1

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Bryonia Eucalyptus Flu Relief
ACONITUM NAPELLUS ROOT BRYONIA CRETICA SUBSP. DIOICA ROOT EUPATORIUM CANNABINUM WHOLE FLOWERING CINCHONA OFFICINALIS BARK EUCALYPTUS GLOBULUS LEAF
ACONITUM NAPELLUS ROOT
BRYONIA CRETICA SUBSP. DIOICA ROOT
SUCROSE
EUPATORIUM CANNABINUM WHOLE FLOWERING
CINCHONA OFFICINALIS BARK
EUCALYPTUS GLOBULUS LEAF

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-2084	48951-2084-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ACONITUM NAPELLUS ROOT	KPD2N7348X	ACTIB
BRYONIA CRETICA SUBSP. DIOICA ROOT	53UB5FH7CX	ACTIB
SUCROSE	C151H8M554	IACT
EUPATORIUM CANNABINUM WHOLE FLOWERING	A5296YC7FS	ACTIB
CINCHONA OFFICINALIS BARK	S003A158SB	ACTIB
EUCALYPTUS GLOBULUS LEAF	S546YLW6E6	ACTIB

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 48 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
SUCROSE	SUCROSE	C151H8M554	ELIXIR / ORAL		18000 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	LIQUID / ORAL		37500 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	INJECTABLE, LIPOSOMAL / INTRAVENOUS		7560 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	TROCHE / BUCCAL	NA		Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	GRANULE, FOR SOLUTION / ORAL		42596 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	TABLET / SUBLINGUAL	109 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	CAPSULE, COATED, EXTENDED RELEASE / ORAL		86 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	TABLET / BUCCAL	109 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	CAPSULE / ORAL		3568 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	GRANULE / ORAL	NA		Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	INJECTION, EMULSION / INTRAVENOUS		970 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	SUSPENSION / ORAL		48209 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	CAPSULE, DELAYED RELEASE / ORAL		955 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	PASTILLE / ORAL	426 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	WAFER / ORAL	155.2 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAVENOUS		2000 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	SUSPENSION/ DROPS / ORAL		3750 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	GRANULE, FOR SUSPENSION, EXTENDED RELEASE / ORAL		18790 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	INJECTION, SUSPENSION, EXTENDED RELEASE / SUBCUTANEOUS		1 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	INJECTION / SUBCUTANEOUS	47.75 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	SOLUTION / RECTAL	35.42 %w/v		Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	POWDER, FOR SOLUTION / ORAL		38666 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	SUPPOSITORY / RECTAL	NA		Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	INJECTION, POWDER, FOR SUSPENSION / INTRAVENOUS	900 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	LOZENGE / BUCCAL	NA		Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / SUBCUTANEOUS		308 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	INJECTION / INTRAVENOUS		1950 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	LOZENGE / TRANSMUCOSAL		1255 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	INJECTION, SUSPENSION, LIPOSOMAL / INTRAVENOUS	9.4 %w/v		Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	TABLET, FILM COATED / ORAL		145 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	SYRUP / ORAL		46400 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	TABLET, CHEWABLE / ORAL		7258 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	SOLUTION / ORAL		70000 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	TABLET, FILM COATED, EXTENDED RELEASE / ORAL	119.12 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	POWDER, FOR SUSPENSION / ORAL		40017 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	DROPS / ORAL	NA		Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	TABLET, COATED / ORAL	516.42 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	SUSPENSION, EXTENDED RELEASE / ORAL		5400 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	POWDER / ORAL		27768 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	TABLET, EXTENDED RELEASE / ORAL	284.54 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	TABLET, DELAYED RELEASE / ORAL	295.33 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	GRANULE, FOR SUSPENSION / ORAL		31885 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	INJECTION, SOLUTION / INTRAVENOUS	NA		Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	CAPSULE, COATED PELLETS / ORAL	59.8 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	TABLET / ORAL		4249 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	CONCENTRATE / ORAL		4800 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	CAPSULE, EXTENDED RELEASE / ORAL		619 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
SUCROSE	SUCROSE	C151H8M554	TROCHE / ORAL	NA		Exact identifier — unii candidate 48 equally ranked IID candidates

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
12742f30-e03b-11de-8a39-0800200c9a66			9a61ae10-e04d-11de-8a39-0800200c9a66	2009-12-03		Exact identifier spl id: 12742f30-e03b-11de-8a39-0800200c9a66 spl set id: 9a61ae10-e04d-11de-8a39-0800200c9a66

Reported adverse events (FAERS/openFDA)#

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