Lithium Carbonicum 3 Special Order
- Manufacturer
- Uriel Pharmacy Inc.
- Effective date
- 2018-05-09
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-02 00:54:53
Label at a glance#
ProductLithium Carbonicum 3 Special Order
Active ingredientLITHIUM CARBONATE
Label structure9 sections
Contacts and useful links#
Websitewww.urielpharmacy.com
www.urielpharmacy.com
www.urielpharmacy.comLabel contents#
Full prescribing information#
INDICATIONS & USAGE SECTION
Directions: FOR ORAL USE ONLY.
DOSAGE & ADMINISTRATION SECTION
Take 3-4 times daily. Ages 12 and older: 1/8 teaspoon. Ages 2-11: 1/16 teaspoon. Under age 2: Consult a doctor.
OTC - ACTIVE INGREDIENT SECTION
Active Ingredient: Lithium carbonicum (Lithium carbonate) 3X
INACTIVE INGREDIENT SECTION
Inactive Ingredient: Lactose
OTC - PURPOSE SECTION
Use: Temporary relief of headache.
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. Contains 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
www.urielpharmacy.com
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Products#
Every source-derived product name is available through these pages.
- Lithium Carbonicum 3 Special Order
- LACTOSE, UNSPECIFIED FORM
- ANHYDROUS LACTOSE
- LITHIUM CARBONATE
- LITHIUM CATION
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-6073 | 48951-6073-4 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| LACTOSE, UNSPECIFIED FORM | J2B2A4N98G | IACT |
| LITHIUM CARBONATE | 2BMD2GNA4V | 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 |
|---|---|---|---|---|---|---|
| c4fa1d3b-f135-e14f-e053-2a95a90a6cfb | 6bc9c8b0-6a6f-3add-e053-2991aa0a2489 | 2021-06-17 | Warnings | 6bc9c8b0-6a6f-3add-e053-2991aa0a2489 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.