FDA.reportPublic FDA data

Barium Conchae Mercurius

Manufacturer
Uriel Pharmacy Inc.
Effective date
2024-12-23
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:29:48

Label at a glance#

ProductBarium Conchae Mercurius
Active ingredientBARIUM IODATE, BERBERIS VULGARIS ROOT BARK, MERCURIC SULFIDE, FERROUS ARSENATE, BARIUM CITRATE, OSTREA EDULIS SHELL, MERCURY
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: Barium iodatum (Barium iodide) 4X, Berberis (Barberry) 4X, Cinnabar (Nat. mercuric sulfide) 6X, Ferrum arsen. (Iron arsenite solution) 6X, Barium citricum (Barium citrate) 8X, Conchae (Oyster shells) 10X, Mercurius vivus (Mercury) 14X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Organic sucrose, Lactose

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Use: Temporary relief of sore throat.

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

Barium Conchae Mercurius PelletsBarium Conchae Mercurius Pellets

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
04cdd491-d111-4bc2-9549-75c575e1bd4bProduct name120200714
8390fb8b-6c75-416c-a9a1-70e8ed493b73Product name120200611
96a528e9-23e2-495f-81b9-ae87df2f7552Product name120191120
3df56c93-5837-4523-aac2-4b1ec48b9676Product name220160719
a883b7cc-d320-41d7-92ae-c873457ae641Product name120151116
bb23e78e-9e64-4037-a1c1-0e1d8762700eProduct name120150325
ef06c001-572c-d95e-42f6-ee83da75673aProduct name120140508
fd21f957-6863-d07b-5a35-250186878716Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-2147-2Barium Conchae Mercurius1350 in 1 BOTTLE, GLASSPELLET13502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-2147BARIUM CONCHAE MERCURIUS PELLET [URIEL PHARMACY INC.]21 package rows20241225_0eff7f73-a663-34ae-e063-6294a90abbf1.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-214748951-2147-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
BARIUM IODATEST2993NJ5JACTIB
BERBERIS VULGARIS ROOT BARK1TH8Q20J0UACTIB
MERCURIC SULFIDEZI0T668SF1ACTIB
FERROUS ARSENATE129CO35H12ACTIB
BARIUM CITRATEJ9X0Y34WC2ACTIB
OSTREA EDULIS SHELL49OY13BE7ZACTIB
MERCURYFXS1BY2PGLACTIB
SUCROSEC151H8M554IACT
LACTOSEJ2B2A4N98GIACT

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
29f29bb8-9bec-77cd-e063-6294a90adb500eff7f73-a663-34ae-e063-6294a90abbf12024-12-23WarningsExact identifier
spl id: 29f29bb8-9bec-77cd-e063-6294a90adb50
spl set id: 0eff7f73-a663-34ae-e063-6294a90abbf1

Reported adverse events (FAERS/openFDA)#

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