Otc - Active Ingredient
monzonite
Evertox Special Bath Preparations
FDA Label NDC 69474-1001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Kmtr Co., Ltd. for the product Evertox Special Bath Preparations (NDC 69474-1001). 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 otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
silica compound
Otc - Purpose
relieve atopic symptom (itching, inflammation and pain), relieve ring worm, relieve stress
Otc - Keep Out Of Reach Of Children
keep out of reach of the children
Indications & Usage
apply on evertox per 100 liter approximately
application part: whole body
apply for 5~30 minutes preferably during bath
keep cool and dry after use
Warnings
do not open the case, in case the case opened by user fault, please keep the ingredients away immediately
Dosage & Administration
for external use only
* Please review the disclaimer below.
