Inactive Ingredients
Alcohol (20% v/v). Purified water
Virex
FDA Label NDC 61657-1027
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 Virex (NDC 61657-1027). 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 inactive ingredients, purpose, keep out of reach of children, indications, warning, pregnancy or breast feeding, safety, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
FOR THE TEMPORARY RELIEF OF HEAVINESS, WEAKNESS, WEARINESS, NUMBNESS, TINGLING, MUSCLE SORENESS OR ACHING
Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN
Indications
INDICATIONS: FOR THE TEMPORARY RELIEF OF HEAVINESS, WEAKNESS, WEARINESS, NUMBNESS, TINGLING, MUSCLE SORENESS OR ACHING
Warning
WARNING: Stop use and call a doctor if symptoms persist or worsen.Contains alcohol: in case of accidental overdose, consult a poison control center immediately
Pregnancy Or Breast Feeding
If pregnant or breast-feeding, consult a healthcare professional before use
Safety
Other information: Tamper resistant for your protection. Use only if safety seal is intact
Directions
DIRECTIONS: Take 6 drops, 4 times a day. For ages 2 to adult
Active Ingredient
Arsenicum alb 12X
Baptisia 3X
Belladonna 12X
Echinacea 3X
Eupatorium perf 12X
Gelsenium 12X
Lycopodium 12X
Nux vom 12X
Phosphoricum ac 12X
Phos 12X
Pyrogenium 30X
Rhus tox 30X
Manufacture
MANUFACTURED FOR
MICRO WEST
P.O. Box 950
DOUGLAS, WY 82633
1-307-358-5066
Label Display
Image Description (Virex)
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