Active Ingredient
ETHYL ALCOHOL 62%
Instant Hand Sanitizer
FDA Label NDC 72036-230
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Harris Teeter for the product Instant Hand Sanitizer (NDC 72036-230). 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, 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
HELPS REDUCE BACTERIA ON THE SKIN.
Warnings
- FLAMMABLE, KEEP AWAY FROM FIRE.
- FOR EXTERNAL USE ONLY.
When Using This Product
AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE EYES THROUGHLY WITH WATER.
Stop Using This Product And Ask Doctor
IF IRRITATION AND REDNESS DEVELOP.
Keep Out Of Reach Of Children
IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.
Directions
APPLY A SMALL AMOUNT IN YOUR PALM AND RUB HANDS TOGETHER BRISKLY UNTIL DRY. CHILDREN UNDER 6 SHOULD BE SUPERVISED WHEN USING THIS PRODUCT.
Other Information
DO NOT STORE ABOVE 110 DEGREES FAHRENHEIT (43 DEGREES CELSIUS).
Inactive Ingredients
WATER (AQUA), GLYCERIN, ISOPROPYL MYRISTATE, PROPYLENE GLYCOL, TOCOPHERYL ACETATE, AMINOMETHYL PROPANOL, CARBOMER, FRAGRANCE, RED 4 (CI 14700), YELLOW 5 (CI 19140).
Front And Back Labels
Image Of Label (Harris)
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