Active Ingredient
Alcohol w/w 70%
Moxe
FDA Label NDC 73333-340
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Nutrix International, Llc. for the product Moxe (NDC 73333-340). 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, use, warnings, do not use, stop use and ask a doctor, keep out of reach of children., directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Use
Use to help reduce bacteria on the skin
Warnings
• For external use only.
• Flammable.
• Keep away from fire or flame.
Do Not Use
Do Not Use Near Eyes. In case of contact, rinse eyes thoroughly with water
Stop Use And Ask A Doctor
If skin irritation develops.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away
Directions
• Place sanitizer on palm, rub hands together.
• Supervise children under 6.
Other Information
Do not store over 110° F
Questions?
Call 1-800-296-3160
Inactive Ingredients
Water (Aqua), Acrylates Copolymer, TEA, Glycerin, Propylene Glycol, Fragrance.
Purpose
Antiseptic
Package
Front Label
Drug Fact
Complete Label
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