Active Ingredients
Arsenicum alb 12X
Belladonna 12X
Cajuputum 4X
Capsicum 3X
Cinchona 12X
Fragaria 12X
Lycopodium 12X
Merc corros 12X
Nitricum ac 12X
Nux vom 12X
Phos 12X
Phytolacca 6X
Rhamnus pursh 3X
Vermafuge -ag Liquid
FDA Label NDC 61657-1026
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 Vermafuge -ag (NDC 61657-1026). 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, keep out of reach of children, warning, other safety information, directions, indications, inactive ingredient, 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 DYSENTERY, FLATULENCE, AND COLIC
Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN
Warning
WARNINGS: 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.
Other Safety Information
OTHER INFORMATION: Tamper resistant for your protection. Use only if safety seal is intact.
Directions
DIRECTIONS: Take 6 drops orally, 4 times a day. For ages 2 to adult
Indications
INDICATIONS: FOR THE TEMPORARY RELIEF OF DYSENTARY, FLATULENCE, AND COLIC
Inactive Ingredient
Alcohol 20% v/v
Purified water
Manufacture
MANUFACTURED FOR
MICRO-WEST
P.O. BOX 950
DOUGLAS, WY 82633
1-307-358-5066
* Please review the disclaimer below.
