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Kali mur - Prescription Drug Labeling

Product NDC Code 44911-0166
Drug Name

Kali mur

Type Brand
Active Ingredients
Potassium chloride 200 [hp_c]/ml
Route ORAL
Dosage Form LIQUID
Labeler Name Energique, Inc.
Packages
Package NDC Code Description
44911-0166-1 30 ml in 1 bottle, dropper (44911-0166-1)

Active ingredient

A list of the active, medicinal ingredients in the drug product.
ACTIVE INGREDIENT: (in each drop): 100% of Kali Muriaticum 200C.

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 and children 5 to 10 drops orally, 1 time daily or as otherwise directed by a health care professional. If symptoms persist for more than 4 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

Inactive ingredient

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

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: May temporarily relieve nasal congestion and chronic ear complaints.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Purpose

Information about the drug product’s indications for use.
INDICATIONS: May temporarily relieve nasal congestion and chronic ear complaints.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Spl product data elements

Usually a list of ingredients in a drug product.
Kali Mur 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: ENERGIQUE SINCE 1987 HOMEOPATHIC REMEDY KALI MUR 200C 1 fl. oz. (30 ml) Kali Mur 200C

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: Dist. by Energique, Inc. 201 Apple Blvd Woodbine, IA 51579 800-869-8078

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: If pregnant or breast-feeding, 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. Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

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