FDA.reportPublic FDA data

Aconitum Bryonia Adult

Manufacturer
Uriel Pharmacy | Uriel Pharmacy Inc.
Effective date
2021-08-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:38:14

Label at a glance#

ProductAconitum Bryonia Adult
Active ingredientATROPA BELLADONNA, EUCALYPTUS GUM, SILVER, ECHINACEA, UNSPECIFIED, CINCHONA OFFICINALIS BARK, EUPATORIUM PERFOLIATUM FLOWERING TOP, ACONITUM NAPELLUS, BRYONIA ALBA ROOT
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR RECTAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Insert 1 suppository as needed.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Echinacea (Purple coneflower) 2X, Atropa belladonna (Nightshade) 3X, China (Peruvian bark) 4X, Eucalyptus (Eucalyptus) 4X, Eupatorium cann. (Hemp agrimony) 4X, Aconitum (Monkshood) 5X, Bryonia (White bryony) 5X, Argentum met. (Silver) 30X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Cocoa butter, Sorbitan Monolaurate, Micronized silica gel

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. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursings, consult a doctor before use. Do not use if safety seals on box are broken or missing.

KEEP REFRIGERATED OR STORE IN COOL, DRY PLACE. REFRIGERATE TO RESOLIDIFY.

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Aconitum Bryonia AdultAconitum Bryonia Adult

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
48951-135148951-1351-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ATROPA BELLADONNAWQZ3G9PF0HACTIB
EUCALYPTUS GUM72T9EZC2VXACTIB
SILVER3M4G523W1GACTIB
SILICON DIOXIDEETJ7Z6XBU4IACT
COCOA BUTTER512OYT1CRRIACT
ECHINACEA, UNSPECIFIED4N9P6CC1DXACTIB
CINCHONA OFFICINALIS BARKS003A158SBACTIB
EUPATORIUM PERFOLIATUM FLOWERING TOP1W0775VX6EACTIB
ACONITUM NAPELLUSU0NQ8555JDACTIB
BRYONIA ALBA ROOTT7J046YI2BACTIB
SORBITAN MONOLAURATE6W9PS8B71JIACT

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
ed248797-857d-41ef-e053-2995a90a4a11c9607d3a-af8b-4ec3-e053-2a95a90a68752022-11-10WarningsExact identifier
spl set id: c9607d3a-af8b-4ec3-e053-2a95a90a6875

Reported adverse events (FAERS/openFDA)#

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