Active Ingredient
Ethyl alcohol 70%
Mius
FDA Label NDC 71887-272
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Mius Industries Corp for the product Mius (NDC 71887-272). 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 ingredient, purpose, uses, warning, warnings and precautions, when using this product, stop use and ask a doctor if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
■Helps reduce bacteria on the skin
■Recommended for repeated use
Warning
For external use only
Warnings And Precautions
Flammable, keep away from fire, sparks, and sources of ignition. Do not store above 104° F/ 40° C
When Using This Product
■Keep out of eyes ■In case of contact with eyes flush thoroughly with water ■Avoid contact with broken skin
Stop Use And Ask A Doctor If
irritation and redness develop and persist for more than 72 hours
Keep Out Of Reach Of Children.
If swallowed get medical help or contact a Poison Control Center immediately
Directions
■Shake well before use due to natural separation ■Spray directly on hands and rub thoroughly ■For children under 6, use adult supervision ■Not recommended for infants
Inactive Ingredients
Water, Apple Cider Vinegar, Tee Tree Essential Oil, Orange Essential Oil, Tangerine Essential Oil, Grapefruit Essential Oil,Vegetable Glycerin, Vitamin E Safflower Oil
* Please review the disclaimer below.
