Otc - Active Ingredient
Alcohol 65% v/v. Purpose: Antiseptic
65% Alcohol Hand Sanitizer (no Water)
FDA Label NDC 74642-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Virgin Scent Inc. for the product 65% Alcohol Hand Sanitizer (no Water) (NDC 74642-001). 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, dosage & administration, warnings, otc - when using, otc - stop use, otc - 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
Otc - Purpose
Antiseptic, Hand Sanitizer
Indications & Usage
HELPS REDUCE BACTERIA ON THE SKIN. RECOMMENDED FOR REPEATED USE.
Dosage & Administration
SQUEEZE A SMALL AMOUNT INTO THE PALMS OF YOUR HANDS AND MASSAGE GENTLY. ALLOW TO DRY WITHOUT WIPING OR RINSING.
Warnings
For external use only. Flammable.Keep away from fire or flame.
Otc - When Using
When using this product, avoid contact with eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin.
Otc - Stop Use
Stop use and ask doctor if irritation or redness developes. or if condition persists for more than 72 hours
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.
Inactive Ingredient
Water, Carbomer 940, Triethanolamine, Glycerin
Other Safety Information
Store below 110 (Degree Fahrenheit). May cause discoloration to certain fabrics and surfaces.
Package Label - Principal Display Panel
236 mL NDC: 74642-001-01
Pdp (74621 003 01)
* Please review the disclaimer below.
