Active Ingredient
Active Ingredient: Alcohol 70% v/v
Scriptsusa Hand Sanitizer Gel
FDA Label NDC 87474-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Energized Solution Corp for the product Scriptsusa Hand Sanitizer (NDC 87474-001). 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, warning, purpose, uses, directions, inactive ingredients, stop use and ask a doctor, 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
Warning
Flammable. Keep away from fire or flame.
For external use only.
Do not use in eyes.
Stop use if irritation or redness develops.
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
Purpose
Antiseptic
Uses
For hand sanitizing to reduce bacteria on the skin when soap and water are not available.
Directions
Apply enough product to cover all hand surfaces. Rub hands together until dry.
Supervise children under 6 years of age to prevent swallowing.
Inactive Ingredients
Purified Water, Glycerin, Carbomer 940, Triethanolamine,Vitmain E
Stop Use And Ask A Doctor
Stop use and ask a doctor if irritation or rash occurs and persists.
Keep Out Of Reach Of Children
Keep out of reach of children.
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