Active Ingredient
Ethyl Alcohol 70% v/v.
Sanaux Hand Sanitizer Antibacterial Gel
FDA Label NDC 75509-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sanloz Group Inc. for the product Sanaux Hand Sanitizer Antibacterial Gel (NDC 75509-001). 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, warnings, directions, otc - keep out of reach of children, inactive ingredients, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antibacterial
Uses
Hand sanitizer to help reduce bacteria on skin.
Warnings
Keep out of reach of children.
When using this product, do not use in or near the eyes. In case of exposure in eyes wash thoroughly with lots of water.
If swallowed do not attempt to induce vomit, seek medical attention or contact poison control center immediately.
This product is intended for external use only. Flammable. Keep away from fire or flame.
Directions
Place enough product in your palm to thoroughly cover both hands. Rub hand together briskly until dry. Children under 6 years of age should be supervised when using this product.
Otc - Keep Out Of Reach Of Children
Inactive Ingredients
Glycerin, Carboxymethylcellulose, Triethanolamine, Water
Package Label.Principal Display Panel
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