OTC - ACTIVE INGREDIENT SECTION
KALI MURIATICUM 30K
KALI MURIATICUM
- Manufacturer
- Seroyal USA | SAN’UP
- Effective date
- 2022-11-07
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:49:27
Label at a glance#
ProductKALI MURIATICUM
Active ingredientPOTASSIUM CHLORIDE
Label structure11 sections
Label contents#
Full prescribing information#
OTC - PURPOSE SECTION
Indications
For the temporary relief of symptoms associated with cold and joint pain
WARNINGS SECTION
WARNING: If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
OTC - PREGNANCY OR BREAST FEEDING SECTION
If pregnant or breastfeeding, ask a health professional before use.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children.
OVERDOSAGE SECTION
In case of overdose, get medical help or contact a Poison Control Center right away.
OTHER SAFETY INFORMATION
Do not use if label perforation is broken
INACTIVE INGREDIENT SECTION
INACTIVE INGREDIENTS: Lactose, sucrose
DOSAGE & ADMINISTRATION SECTION
DIRECTIONS: Adults: Take five granules three times daily or as recommended by your healthcare practitioner. Children: Take three granules and follow adult directions.
INDICATIONS & USAGE SECTION
Indications
For the temporary relief of symptoms associated with cold and joint pain
DIRECTIONS: Adults: Take five granules three times daily or as recommended by your healthcare practitioner. Children: Take three granules and follow adult directions.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Homepathic Remedy
NDC 62106-5098-4
KALI MURIATICUM
Potassium chloride
140 granules
Indications
For the temporary relief of symptoms associated with cold and joint pain
Products#
Every source-derived product name is available through these pages.
- KALI MURIATICUM
- Potassium chloride
- LACTOSE, UNSPECIFIED FORM
- ANHYDROUS LACTOSE
- POTASSIUM CATION
- SUCROSE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 62106-5098 | 62106-5098-4 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| LACTOSE, UNSPECIFIED FORM | J2B2A4N98G | IACT |
| POTASSIUM CHLORIDE | 660YQ98I10 | ACTIB |
| SUCROSE | C151H8M554 | 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 |
|---|---|---|---|---|---|---|
| 06bf8f3e-c274-31ae-e063-6294a90a728d | 7b495559-50f6-1c23-e053-2991aa0af536 | 2023-10-02 | Warnings | 7b495559-50f6-1c23-e053-2991aa0af536 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.