Drug Facts
Drug Facts
Hand Sanitizer Gel
FDA Label NDC 72449-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ls Promotions Inc. for the product Hand Sanitizer Gel (NDC 72449-101). 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 drug facts, active ingredient, purpose, uses, warnings, when using this product, stop use and ask a doctor, 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
Active Ingredient
Ethanol 62%
Purpose
ANTISEPTIC
Uses
TO HELP DECREASE BACTERIA ON HANDS
Warnings
FOR EXTERNAL USE ONLY. FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME
When Using This Product
KEEP OUT OF EYES. IN CASE OF CONTACT WITH EYES, FLUSH THOROUGHLY WITH WATER AND THEN SEEK MEDICAL ADVICE.
Stop Use And Ask A Doctor
IF IRRITATION OR REDNESS DEVELOPS
Keep Out Of Reach Of Children
IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.
Directions
PLACE ENOUGH PRODUCT IN YOUR PALM TO THOROUGHLY COVER HAND. RUB HANDS TOGETHER BRISKLY UNTIL DRY. FOR CHILDREN UNDER 6 YEARS OLD, USE ADULT SUPERVISION.
Other Information
DO NOT STORE ABOVE 100° F.
Inactive Ingredients
Inactive Ingredients: water, glycerin, propylene glycol, isopropyl myristate, tocopheryl acetate, carbomer, triethanolamine, fragrance
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