Barium Conchae

Manufacturer
Uriel Pharmacy Inc.
Effective date
2017-08-16
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:09:38

Label at a glance#

ProductBarium Conchae
Active ingredientMERCURIC SULFIDE, BARIUM CITRATE, BERBERIS VULGARIS ROOT BARK, FERROUS ARSENATE, OSTREA EDULIS SHELL, BARIUM IODATE
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Take 3-4 times daily. Ages 12 and older: 10 drops. Ages 2-11: 5 drops. 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 arsenicosum (Nat. ferric arsenate) 6X, Barium citricum (Barium citrate) 8X, Conchae (Oyster shells) 10X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Distilled water, Organic cane alcohol, Lactose

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: 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 Made with care by Uriel, East Troy, WI 53120 www.urielpharmacy.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

barconliqbarconliq

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-2026-3Barium Conchae1 mL in 1 BOTTLE, DROPPERLIQUID14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-2026BARIUM CONCHAE LIQUID [URIEL PHARMACY INC.]4Legacy NDC, 1 package rows20180509_34a0b4ee-747e-4ca0-af89-80b232172efe.zip

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
48951-202648951-2026-3

Ingredients#

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

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

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
56e16db3-dbba-494c-e054-00144ff8d46c34a0b4ee-747e-4ca0-af89-80b232172efe2017-08-16WarningsExact identifier
spl id: 56e16db3-dbba-494c-e054-00144ff8d46c
spl set id: 34a0b4ee-747e-4ca0-af89-80b232172efe

Reported adverse events (FAERS/openFDA)#

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