Active Ingredient
ETHYL ALCOHOL 62 PERCENT
Sanitizer
FDA Label NDC 41520-235
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by American Sales for the product Sanitizer (NDC 41520-235). 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 using this product and ask doctor if, 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
ANTIMICROBIAL
Uses
TO HELP REDUCE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE. RECOMMENDED FOR REPEATED USE.
Warnings
FOR EXTERNAL USE ONLY. FLAMMABLE KEEP AWAY FROM FIRE OR FLAME.
When Using This Product
AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE WITH WATER.
Stop Using This Product And Ask Doctor If
IRRITATION OR RASH DEVELOPS AND LASTS.
Keep Out Of Reach Of Children
IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.
Directions
SPRAY ENOUGH PRODUCT IN YOUR PALM TO THOROUGHLY COVER YOUR HANDS.
RUB HANDS TOGETHER BRISKLY UNTIL DRY.
CHILDREN UNDER 6 YEARS OF AGE SHOULD BE SUPERVISED WHEN USING THIS PRODUCT.
Other Information
STORE AT A TEMPERATURE BELOW 110 DEGREES FAHRENHEIT (43 DEGREES CELSIUS).
Inactive Ingredients
WATER, PROPYLENE GLYCOL, GLYCERIN, FRAGRANCE, ISOPROPYL MYRISTATE, TOCOPHERYL ACETATE, ALOE BARBADENSIS LEAF EXTRACT.
Package Label.Principal Display Panel
Image Of Hand Sanitizer (Coss1)
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