Active Ingredient
ETHYL ALCOHOL 65%
Instant Hand Sanitizer
FDA Label NDC 37808-254
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 Instant Hand Sanitizer (NDC 37808-254). 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
ANTISEPTIC
Uses
TO HELP REDUCE BACTERIA ON THE SKIN.
Warnings
FOR EXTERNAL USE ONLY. FLAMMABLE, KEEP WAY FROM FIRE OR FLAME.
When Using This Product
AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE EYES WITH WATER.
Stop Using This Product And Ask Doctor If
IRRITATION OR REDNESS 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
WET HANDS THROUGHLY AND RUB TOGETHER UNTIL DRY.
Other Information
STORE AT A TEMPERATURE BELOW 110 DEGREES FAHRENHEIT (43 DEGREES CELSIUS).
Questions And Comments
1-866-695-3030
Inactive Ingredients
WATER, ISOPROPYL ALCOHOL, GLYCERIN, CARBOMER, AMINOMETHYL PROPANOL, FRAGRANCE, PROPYLENE GLYCOL, ISOPROPYL MYRISTATE, ALOE BARBADENSIS LEAF JUICE, TOCOPHERYL ACETATE, BLUE 1 (CI 42090), YELLOW 5 (CI 19140).
Package Label.Principal Display Panel
Image Of Hand Sanitizer (Hs1)
* Please review the disclaimer below.
