Active Ingredients:
ETHYL ALCOHOL 65%
Hand Sanitizer
FDA Label NDC 74642-002
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 Hand Sanitizer (NDC 74642-002). 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 ingredients:, purpose, uses:, warnings:, when using this product,, stop use and ask doctor, keep out of reach of children., directions:, 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 FROMFIRE OR FLAME.
When Using This Product,
AVOID CONTACT WITH EYES. IN CASE OF CONTACT WITH EYES, FLUSH THOROUGHLY WITH WATER. AVOID CONTACT WITH BROKEN SKIN.
Stop Use And Ask Doctor
IF IRRITATION OR REDNESS DEVELOPS, OR IF CONDITION PERSISTS FOR MORE THAN 72 HOURS.
Keep Out Of Reach Of Children.
IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.
Directions:
DISPENSE ONE PUMP OF SANITIZER ONTO HANDS AND RUB TOGETHER UNTIL DRY. USE AS NEEDED. FOR CHILDREN UNDER 6, USE WITH ADULT SUPERVISION. NOT RECOMMENDED FOR INFANTS.
Other Info:
STORE BELOW 110 (DEGREES FAHRENHEIT). MAY CAUSE DISCOLORATION TO CERTAIN FABRICS AND SURFACES.
Inactive Ingredients
WATER, ALOE BARBADENSIS LEAF EXTRACT, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, ALCOHOL, TETRAHYDROXYPROPYL ETHYLENEDIAMINE
Package Labeling:
Label (Label)
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