Otc - Active Ingredient
ETHYL ALCOHOL 62%
Hand Sanitizer
FDA Label NDC 55316-268
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dza Brands Llc for the product Hand Sanitizer (NDC 55316-268). 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 otc - active ingredient, purpose, uses, warnings, when using this product, stop using and ask a 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
HAND SANITIZER TO HELP REDUCE BACTERIA ON THE SKIN.
Warnings
FOR EXTERNAL USE ONLY. FLAMMABLE. KEEP AWAY FROM FIRE.
When Using This Product
AVOID CONTACT WITH THE EYES. IF CONTACT OCCURS, RINSE WITH WATER.
Stop Using And Ask A 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
PUT ENOUGH PRODUCT IN YOUR PALM TO THROUGHLY 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 FAHRENHEIT (43 DEGREES CELCIUS).
Inactive Ingredient
WATER, GLYCERIN, ISOPROPYL MYRISTATE, PROPYLENE GLYCOL, TOCOPHERYL ACETATE, AMINOMETHYL PROPANOL, CARBOMER, FRAGRANCE.
Package Label.Principal Display Panel
Image Of Hand Sanitizer (Hs1)
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