Active Ingredient[S]
Alcohol 70%
Moxe
FDA Label NDC 73333-011
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 73333-011). 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[s], use[s], warnings, do not use, stop use and ask, 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[S]
Use to help reduce bacteria on the skin.
Warnings
• For external use only.
• Flammable.
• Keep away from heat 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 contacta Poison Control Center right away
Directions
• Place sanitizer on palm, rub hands together.
• Supervise children under 6 years of age.
Other Information
Do not store over 110° F
Inactive Ingredients
Water (Aqua), Glycerin, Propylene Glycol, Carbomer, Triethanolamine, Fragrance
Purpose
Antiseptic
Artwork
Label
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