Active Ingredient
ETHYL ALCOHOL 62%
Waterless Hand Sanitizer
FDA Label NDC 59450-231
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by The Kroger Company for the product Waterless Hand Sanitizer (NDC 59450-231). 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, purpose, uses, warnings, when using this product, stop use and ask a 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
TO DECREASE BACTERIA ON THE SKIN
Warnings
FOR EXTERNAL USE ONLY, FLAMMABLE, KEEP AWAY FROM HEAT AND FLAME.
When Using This Product
KEEP OUT OF EYES. IN CASE OF CONTACT WITH EYES, FLUSH THOROUGHLY WITH WATER. DO NOT INHALE OR INGEST. AVOID CONTACT WITH BROKEN SKIN.
Stop Use And Ask A Doctor
IF SKIN IRRITATION DEVELOPS
Keep Out Of Reach Of Children
IN CASE OF ACCIDENTAL INGESTION, SEEK PROFESSIONAL ASSISTANCE OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.
Directions
WET HANDS THOROUGHLY WITH PRODUCT AND ALLOW TO DRY WITHOUT WIPING. FOR CHILDREN UNDER SIX, USE ONLY UNDER ADULT SUPERVISION. NOT RECOMMENDED FOR INFANTS.
Questions
1-800-632-6900
Other Information
STORE AT ROOM TEMPERATURE
Inactive Ingredients
WATER, GLYCERIN, ISOPROPYL MYRISTATE, PROPYLENE GLYCOL, TOCOPHERYL ACETATE, AMINOMETHYL PROPANOL, CARBOMER, FRAGRANCE
Package Label.Principal Display Panel
Image Of Label (Khs8)
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