Active Ingredient
ETHYL ALCOHOL 62%
Hand Sanitizer
FDA Label NDC 37808-238
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Heb for the product Hand Sanitizer (NDC 37808-238). 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, if skin irritation develops,, otc - 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
ANTIBACTERIAL
Uses:
TO DECREASE BACTERIA ON THE SKIN.
Warnings
FOR EXTERNAL USE ON THE HANDS ONLY. IN CASE OF ACCIDENTAL INGESTION, SEEK MEDICAL ASSISTANCE OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.
When Using This Product
AVOID CONTACT WITH EYES. IF EYE CONTACT OCCURS, FLUSH THOROUGHLY WITH WATER. AVOID CONTACT WITH BROKEN SKIN.
If Skin Irritation Develops,
DISCONTINUE USE AND CONTACT A DOCTOR.
Otc - Keep Out Of Reach Of Children
FOR CHILDREN UNDER 6, USE ONLY WITH ADULT SUPERVISION. NOT RECOMMENDED FOR USE ON INFANTS.
Directions:
PUT A SMALL AMOUNT IN YOUR PALM AND BRISKLY RUB HANDS TOGETHER UNTIL DRY.
Other Information
FLAMMABLE. KEEP AWAY FROM HEAT AND FLAME.
Inactive Ingredients
WATER, GLYCERIN, ALUMINA, ISOPROPYL MYRISTATE, TITANIUM DIOXIDE, BUTYROSPERMUM PARKII (SHEA BUTTER) EXRACT, TOCOPHERYL ACETATE, CARBOMER, AMINOMETHYL PROPANOL, FRAGRANCE.
Package Label.Principal Display Panel
Image Of Hand Sanitizer (Hcfhs)
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