Total Mercury Liquid
FDA Label NDC 61657-0961

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 Total Mercury (NDC 61657-0961). 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, otc - keep out of reach of children, indications, warning, directions, inactive ingredient, manufacture, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients

MERCURIUS VIVUS [HPUS]  12X,30X,200C,1M

Contains equal volumes of each ingredient.

Purpose

FOR THE TEMPORARY RELIEF OF DIZZINESS, DISCOURAGED, DEPRESSION, PAINFUL DRYNESS OF THROAT

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN

Indications

INDICATIONS :FOR THE TEMPORARY RELIEF OF DIZZINESS,FEELING  DISCOURAGED, DEPRESSION, PAINFUL DRYNESS OF THROAT

Warning

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

Directions

DIRECTIONS: ORALLY 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

DOUGLAS, WY 82633

1-307-358-5066

Label

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