Active Ingredient
EHTANOL 62%. PURPOSE: ANTISEPTIC
Hand Sanitizer
FDA Label NDC 75601-0001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Punch Studio, Llc for the product Hand Sanitizer (NDC 75601-0001). 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, do not use, keep out of reack of children., directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
ANTISEPTIC
Uses
- TO HELP REDUCE BACTERIA ON HANDS
- WHEN WATER & SOAP ARE NOT AVAILABLE
Warnings
- FOR EXTERNAL USE ONLY
- KEEP OUT OF EYES
- FLAMMABLE, KEEP AWAY FROM HEAT OR FLAME
Do Not Use
- ON CHILDREN LESS THAN 2 YEARS OF AGE
- ON OPEN SKIN WOUNDS
Keep Out Of Reack Of Children.
IF SWALLOWED, GET MEDICAL HELP OR CALL A POISON CONTROL VENTER RIGHT AWAY.
Directions
- APPLY AS NEEDED INTO PALM OF HANDS, RUB HANDS TOGETHER UNTIL DRY
- SUPERVISE CHILDREN UNDER 6 YEARS OLD
Inactive Ingredients
WATER, TRIETHANOLAMINE, CARBOMER, GLYCERIN, PROPYLENE GLYCOL, ALOE BARBADENSIS EXTRACT, TOCOPHERYL ACETATE
Package Label - Principal Display Panel
150 mL NDC: 75601-0001-1
Front & Back Labels (Cleanslate Labels)
* Please review the disclaimer below.
