Met-tox Liquid
FDA Label NDC 61657-0526

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by White Manufacturing Inc Dba Micro-west for the product Met-tox (NDC 61657-0526). 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, otc - purpose, otc - keep out of reach of children, other information, indications & usage, warnings, directions, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients

ARSENICUM ALBUM 12X

AVENA SATIVA 3X
BERBERIS VULGARIS 3X

LYCOPODIUM CLAVATUM 12X

NATRUM MURIATICUM 12X

NUX VOMICA 12X

PHYTOLACCA DECANDRA 3X

RHAMNUS FRANGULA 3X

SOLIDAGO VIRGAUREA 3X

TRIFOLIUM PRATENSE 3X

Otc - Purpose

FOR THE TEMPORARY RELIEF OF EXHAUSTION, WEAKNESS, ACHING, SORENESS AND RESTLESSNESS

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN

Other Information

TAMPER RESISTANT FOR YOUR PROTECTION. USE ONLY IF SEAL IS INTACT

Indications & Usage

INDICATIONS: FOR THE TEMPORARY RELIEF OF EXHAUSTION, WEAKNESS, ACHING, SORENESS AND RESTLESSNESS

Warnings

WARNING:STOP USE AND CALL A DOCTOR IF SYMPTOMS PERSIST OR WORSEN. IF PREGNANT OR BREAST FEEDING, CONSULT A HEALTHCARE PROFESSIONAL BEFORE USE. CONTAINS ALCOHOL: IN CASE OF ACCIDENTAL OVERDOSE, CONSULT A POISON CONTROL CENTER IMMEDIATELY

Directions

DIRECTIONS:TAKE 6 DROPS ORALLY, 4 TIMES A DAY. FOR AGES 2 TO ADULT

Inactive Ingredient

ALCOHOL (20% V/V) PURIFIED WATER

Manufacture

MANUFACTURED FOR MICRO-WEST

P.O. BOX 950

DOUGLAS, WY 82633

1-307-358-5066

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