Micox Solution/ Drops
FDA Label NDC 17089-420

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Guna Spa for the product Micox (NDC 17089-420). 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 active ingredients/purpose, uses, warnings, pregnancy, directions, questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients/Purpose

ASPERGILLUS NIGER    12X, 30X, 200X    DETOXIFICATION
CANDIDA ALBICANS    12X, 30X, 200X    DETOXIFICATION
DL-MALIC ACID        6X,12X, 30X    CELL METABOLISM
HYDROCOTYLE ASIATICA    6X    CELL METABOLISM
MERCURIUS CORROSIVUS    6X    CELL METABOLISM
MUCOR MUCEDO        12X, 30X, 200X    DETOXIFICATION
NATRUM OXALACETICUM    6X,12X, 30X    CELL METABOLISM
PINK TRUMPET TREE    4X    DETOXIFICATION
SULPHUR            6X    DETOXIFICATION

Uses

For the temporary relief of symptoms related to dysbiosis secondary to yeast overgrowth such as: skin rashes, itching, gas and bloating

Warnings

Stop use and ask doctor if symptoms of skin rashes, itching, gas and bloating worsen or persist more than 5 days

Keep this and all medicines out of reach of children

Pregnancy

If pregnant or breast-feeding ask a doctor before use

Directions

Take 15 minutes before meals
Adults and children 12 years and older    20 drops in a little water, 2 times per day
Children  between 12 years and 6 years of age    10 drops in a little water, 2 times per day
Children under 6 years     5 drops in a glass of water, 2 times per day

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