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#
Contacts and useful links#
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
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48951-2026-3 | Barium Conchae | 1 mL in 1 BOTTLE, DROPPER | LIQUID | 1 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-2026 | BARIUM CONCHAE LIQUID [URIEL PHARMACY INC.] | 4 | Legacy NDC, 1 package rows | 20180509_34a0b4ee-747e-4ca0-af89-80b232172efe.zip |
Products#
Every source-derived product name is available through these pages.
- Barium Conchae
- MERCURIC SULFIDE
- MERCURIC CATION
- BARIUM CITRATE
- BARIUM CATION
- LACTOSE
- ALCOHOL
- WATER
- BERBERIS VULGARIS ROOT BARK
- FERROUS ARSENATE
- OSTREA EDULIS SHELL
- BARIUM IODATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-2026 | 48951-2026-3 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| MERCURIC SULFIDE | ZI0T668SF1 | ACTIB |
| BARIUM CITRATE | J9X0Y34WC2 | ACTIB |
| LACTOSE | J2B2A4N98G | IACT |
| ALCOHOL | 3K9958V90M | IACT |
| WATER | 059QF0KO0R | IACT |
| BERBERIS VULGARIS ROOT BARK | 1TH8Q20J0U | ACTIB |
| FERROUS ARSENATE | 129CO35H12 | ACTIB |
| OSTREA EDULIS SHELL | 49OY13BE7Z | ACTIB |
| BARIUM IODATE | ST2993NJ5J | ACTIB |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 56e16db3-dbba-494c-e054-00144ff8d46c | 34a0b4ee-747e-4ca0-af89-80b232172efe | 2017-08-16 | Warnings | 56e16db3-dbba-494c-e054-00144ff8d46c 34a0b4ee-747e-4ca0-af89-80b232172efe |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
