Otc - Active Ingredient
Alcohol 75% v/v. Purpose: Antiseptic
Hand Sanitizer
FDA Label NDC 74235-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Quality Innovations Inc. for the product Hand Sanitizer (NDC 74235-001). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Antiseptic, Hand Sanitizer
Indications & Usage
Help decrease bacteria on skin.
Recommended for repeated use
Warnings
For external use only
Flammable, keep away from fire or flame
Do not apply around eyes.
Otc - When Using
When using this product, avoid contact with eyes. In case of contact, flush eyes with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develops & condition persists for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep our of reach of Children. Children must be supervised in use of this product.
Dosage & Administration
Pump as needed into your palms & thoroughly spread on both hands.
Other Safety Information
Do not store above 110F
Inactive Ingredient
Water, Glycerin, Triethanolamine, Carbomer, Dimethylamino
Package Label - Principal Display Panel
60 mL NDC: 74235-001-01
Pdp (74235 001 01)
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