Active Ingredient Purpose
Ethyl Alcohol 62% ........................................Antiseptic
Antibacterial Hand Sanitizer
FDA Label NDC 71246-5030
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Jfl Enterprises, Inc for the product Antibacterial Hand Sanitizer (NDC 71246-5030). 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, purpose, use, warnings, keep out of reach of children, directions, inactive ingredient, stop and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic Hand Sanitizer
Use
Decrease bacteria on hands
Warnings
External Use Only.
Flammable: Keep away from flame or high heat
Keep Out Of Reach Of Children
if swallowed get medical help or contact a Poison Control Center right away.
Directions
Rub hands thoroughly with product and allow to dry.
Inactive Ingredient
Aminomethyl Propanol, Carbomer, Isopropyl Alcohol, Water
Stop And Ask A Doctor If
Irritation or redness develop.
How Supplied
Product: 71246-50309
NDC: 71246-5030-1 59 mL in a BOTTLE
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