Candicide
FDA Label NDC 62713-930

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Meditrend, Inc. Dba Progena Professional Formulations for the product Candicide (NDC 62713-930). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, indications & usage, warnings, otc - stop use, otc - do not use, otc - pregnancy or breast feeding, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Active Ingredients (HPUS): Baptisia Tinctoria 3X, Borax 30X,
Calcarea Carbonica 30X, Candida Albicans (12X, 30x, 60x, 100x, 500x), Kreosotum 30X,
Lycopodium Clavatum 30X, Nux Vomica 30X, Phosphoricum
Acidum 30X, Pulsatilla 30X, Sepia 30X. 

Otc - Purpose


Purpose:
Support for the Treatment of Symptoms Associated with
Candida Albicans.

Indications & Usage

Use: This product is a Homeopathic Dilution, formulated to help
improve the body’s immunity in the treatment of diagnosed
Candida Albicans.

Warnings

Warnings:

Use only as directed.

Dosage & Administration

Directions:Adults (12 and Older) take 15 drops under the
tongue three times daily. Children (11 and Younger) take 10 drops
under the tongue three times daily or as directed by your health
care professional. Consult a Physician for use in children under
12 years of age. Not Recommended for Children Under 2
Years of Age.

Other Safety Information

Other Information: Do not use if TAMPER EVIDENT seal
around neck of bottle is missing or broken.

Inactive Ingredient

Inactive Ingredients: Demineralized water and 25% USP Ethanol.

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