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Kali muriaticum - Prescription Drug Labeling

Product NDC Code 71753-8005
Drug Name

Kali muriaticum

Type Generic
Active Ingredients
Potassium chloride 6 [hp_x]/ml
Route ORAL
Dosage Form SPRAY
Labeler Name Ratis, LLC
Packages
Package NDC Code Description
71753-8005-1 30 ml in 1 bottle, spray (71753-8005-1)

Active ingredient

A list of the active, medicinal ingredients in the drug product.
ACTIVE INGREDIENT: Kai Muriaticum 6X.

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
DIRECTIONS: 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.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
INACTIVE INGREDIENTS: Demineralized Water, Organic Ethanol 20%

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
INDICATIONS: 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.

Purpose

Information about the drug product’s indications for use.
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.

Spl product data elements

Usually a list of ingredients in a drug product.
Kali Muriaticum Kali Muriaticum POTASSIUM CHLORIDE POTASSIUM CATION WATER ALCOHOL

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
PACKAGE LABEL DISPLAY: NDC 71753-8005-1 LACTOSE FREE Anna's REMEDIES Kali Muriaticum HOMEOPATHIC ORAL SPRAY 1 FL. OZ (30ML) Kai Muriaticum

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
KEEP OUT OF REACH OF CHILDREN: Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
QUESTIONS: Comments? Visit HomeopathyStore.com or call (888) 405-7551. Distributed by: Ratis, LLC, 211 E. Lombard St, STE 303, Baltimore, MD 21202

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
WARNINGS: 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.

Disclaimer: Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API