Active Ingredients:
ETHYL ALCOHOL 65%
Instant Hand Sanitizer Gel
FDA Label NDC 75248-000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Icarcover Inc. for the product Instant Hand Sanitizer (NDC 75248-000). 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, use:, warnings, when using this product, otc - stop use, 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
Use:
HELP REDUCES 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, FLUSH THOROUGHLY WITH WATER. AVOID CONTACT WITH BROKEN SKIN.
Otc - Stop Use
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°F. MAY CAUSE DISCOLORATION TO CERTAIN FABRICS AND SURFACES.
Inactive Ingredients:
WATER, CARBOMER, TRIETHANOLAMINE
Package Labeling:
Label (Label)
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