Kali Muriaticum

Manufacturer
Ratis, LLC
Effective date
2022-01-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:15:37

Label at a glance#

ProductKali Muriaticum
Active ingredientPOTASSIUM CHLORIDE
Label structure9 sections

Indications and uses

Helps relieve colds and coughs with white discharges, runny nose, tonsillitis, & skin burns.** **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Dosage and administration

Adults: 2 sprays 3 times a day or as needed. Children 2-12: 1 spray as above. For children 12 and under, consult a doctor.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT:

OTC - ACTIVE INGREDIENT SECTION

Kai Muriaticum 6X.

USES:

OTC - PURPOSE SECTION

Helps relieve colds and coughs with white discharges, runny nose, tonsillitis, & skin burns.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

WARNINGS SECTION

For oral use only.

If pregnant or breast-feeding, or if symptoms persist or worsen, ask a health care professional.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Do not use if tamper evident seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults: 2 sprays 3 times a day or as needed.

Children 2-12: 1 spray as above. For children 12 and under, consult a doctor.

INDICATIONS:

INDICATIONS & USAGE SECTION

Helps relieve colds and coughs with white discharges, runny nose, tonsillitis, & skin burns.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, Organic Ethanol 20%

QUESTIONS:

OTC - QUESTIONS SECTION

Comments? Visit

HomeopathyStore.com

or call (888) 405-7551.

Distributed by:

Ratis, LLC,

211 E. Lombard St, STE 303,

Baltimore, MD 21202

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 71753-8005-1

LACTOSE FREE

Anna's

REMEDIES

Kali Muriaticum

HOMEOPATHIC ORAL SPRAY

1 FL. OZ (30ML)

Kai MuriaticumKai Muriaticum

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71753-8005KALI MURIATICUM SPRAY [RATIS, LLC]2Legacy NDC20220121_ae82bd5a-af81-4376-841d-888faffb120e.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71753-800571753-8005-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
POTASSIUM CHLORIDE660YQ98I10ACTIM
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

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
fe104583-be74-40ea-a8d9-e1843a552893ae82bd5a-af81-4376-841d-888faffb120e2022-01-20WarningsExact identifier
spl id: fe104583-be74-40ea-a8d9-e1843a552893
spl set id: ae82bd5a-af81-4376-841d-888faffb120e

Reported adverse events (FAERS/openFDA)#

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