Active Ingredient
ETHYL ALCOHOL 62%
Hand Sanitizer
FDA Label NDC 74598-111
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sunshine Tape Products Llc for the product Hand Sanitizer (NDC 74598-111). 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, otc - keep out of reach of children, directions, 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
ANTISEPTIC
Uses
Helps reduce bacteria on the skin. Recommended for repeated use.
Warnings
For external use only. Flammable. Keep away from fire or flame. When using this product avoid contact with eyes. In case of contact flush thoroughly with water. Avoid contact with open skin. Stop use and ask doctor if irritation or rash develops.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.
Directions
Dispense enough product onto hands and rub together quickly until dry. Use as needed. Children under 6 years of age, use only under adult supervision.
Inactive Ingredients
Purified water, Propylene Glycol, Glycerin, Carbomer, Triethanolamine, Tocopherol Acetate, Coconut Oil, Aloe Vera gel, Fragrance
* Please review the disclaimer below.
