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Kali phos. aurum - Prescription Drug Labeling

Product NDC Code 48951-6011
Drug Name

Kali phos. aurum

Type Generic
Active Ingredients
Silicon dioxide 5 [hp_x]/1
Potassium phosphate, monobasic 6 [hp_x]/1
Gold 10 [hp_x]/1
Ferrous sulfate 5 [hp_x]/1
Route ORAL
Dosage Form TABLET
Labeler Name Uriel Pharmacy Inc.
Packages
Package NDC Code Description
48951-6011-4 250 tablet in 1 bottle, glass (48951-6011-4)

Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredients: 100gm contains: 3.3gm Kali phos. (Potassium dihydrogenphosphate) 6X, 3.3gm Aurum met. (Metallic gold) 10X, 2gm Ferrum sulf. (Iron sulfate) 5X, 0.8gm Quartz (Rock crystal) 5X

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.
Take 3-4 times daily. Ages 12 and older: 1-2 tablets. Ages 2-11: 1 tablet. Under age 2: Consult a doctor.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients: Microcrystalline cellulose, Micronized silica gel, Magnesium stearate

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.
Directions: FOR ORAL USE ONLY.

Purpose

Information about the drug product’s indications for use.
Uses: Temporary relief of nervousness and exhaustion.

Spl product data elements

Usually a list of ingredients in a drug product.
Kali phos. Aurum Kali phos. Aurum SILICON DIOXIDE SILICON DIOXIDE MICROCRYSTALLINE CELLULOSE MAGNESIUM STEARATE POTASSIUM PHOSPHATE, MONOBASIC PHOSPHATE ION GOLD GOLD FERROUS SULFATE FERROUS CATION

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.
Kali phos. Aurum Tablet

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.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions? Call 866.642.2858 Uriel, East Troy, WI 53120 www.urielpharmacy.com

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: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Contains lactose. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety 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