Active Ingredients
Aconitum nap 12X
Arsenicum alb 12X
Calc carb 12X
Ignatia 12X
Lachesis 15X
Passiflora 3X
Phosphorus 12X
Pulsitilla 12X
Scutellaria 3X
Valeriana 3X
Anxiolix Liquid
FDA Label NDC 61657-0006
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 Anxiolix (NDC 61657-0006). 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, inactive ingredient, purpose, keep out of reach of children, indications, warning, directions, manufacture, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Alcohol (2% v/v), Purified water
Alcohol (20%, v/v)
Purpose
TEMPORARY RELIEF OF ANXIETY, SLEEPLESSNESS, NERVOUSNESS
Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN
Indications
INDICATIONS: FOR THE TEMPORARY RELIEF OF ANXIETY, SLEEPLESSNESS, NERVOUSNESS
Warning
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.
Manufacture
MANUFACTURED FOR
MICRO-WEST
DOUGLAS, WY 82633
1-307-358-5066
* Please review the disclaimer below.
