Websitewww.remedymakers.com
www.remedymakers.com
www.remedymakers.comKALI CARBONICUM
- Manufacturer
- REMEDY MAKERS
- Effective date
- 2011-12-27
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:03:29
Label at a glance#
ProductKALI CARBONICUM
Active ingredientPOTASSIUM CARBONATE
Label structure8 sections
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - PURPOSE SECTION
SHARP AND CUTTING PAIN, WEAKNESS, LABOR PAINS, OR OTHER INDICATIONS
OTC - ACTIVE INGREDIENT SECTION
POTASSIUM CARBONATE
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
WARNING:Keep this and all medications out of reach of children.
INDICATIONS & USAGE SECTION
INDICATIONS: To be use according to standard
homeopathic indications, for self-limiting conditions such as these
indicated above or as directed by a physician.
WARNINGS SECTION
WARNING: Use only if cap and seal are unbroken. If symptoms persist for more than 3 days or worsen, discontinue (STOP) use and consult your physician. As with any drug. If you are pregnant or nursing (breast-feeding) a baby, seek the advise of a health professional before using this product. Store tightly closed in a cool area.
DOSAGE & ADMINISTRATION SECTION
Directions:(adult/children)
Dissolve 3 or 4 pellets in mouth or under tongue 3 times a day or as
directed by a physician. Children 2 years and older take 1/2 the adult
dose.
INACTIVE INGREDIENT SECTION
Inactive Ingredient: Lactose and Sucrose. Free from yeast, wheat, corn and soy.
OTC - QUESTIONS SECTION
Questions or comments.(877)REM4YOU. Fax (909)594-4205 Pomona, CA. 91768. USA www.remedymakers.com
Other information: Contain approx.145 - 150 pellets.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 10191-1665-2 | 2019-11-13 | C162847 | 48780-1 | 97449f38-c4f1-f6ea-e053-dbdaa90aa703 | KALI CARBONICUM 6C (Potassium Carbonate) |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 10191-1665-2 | KALI CARBONICUM | 145 in 1 VIAL, GLASS | PELLET | 145 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 10191-1665 | KALI CARBONICUM (POTASSIUM CARBONATE) PELLET [REMEDY MAKERS] | 1 | Legacy NDC, 1 package rows | 20111228_ad82631d-7c0e-4d54-b1dc-a33c4b5f119e.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| POTASSIUM CARBONATE | ACTIVE INGREDIENT | BQN1B9B9HA | 1 | |
| POTASSIUM CATION | ACTIVE MOIETY | 295O53K152 | 1 |
Products#
Every source-derived product name is available through these pages.
- KALI CARBONICUM
- POTASSIUM CARBONATE
- POTASSIUM CATION
- SUCROSE
- LACTOSE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 10191-1665 | 10191-1665-2 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| POTASSIUM CARBONATE | BQN1B9B9HA | ACTIB |
| SUCROSE | C151H8M554 | IACT |
| LACTOSE | J2B2A4N98G | IACT |
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 |
|---|---|---|---|---|---|---|
| beff73bc-c5b8-4b95-8c8e-2c61a2067cb6 | ad82631d-7c0e-4d54-b1dc-a33c4b5f119e | 2011-12-27 | Warnings | beff73bc-c5b8-4b95-8c8e-2c61a2067cb6 ad82631d-7c0e-4d54-b1dc-a33c4b5f119e |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.