Otc - Active Ingredient
Active Ingredient: Ethyl Alcohol 63%
Ili Hand Sanitizer
FDA Label NDC 50859-100
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Strong Brands, Inc. for the product Ili Hand Sanitizer (NDC 50859-100). 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, otc - purpose, indications & usage, warnings, otc - stop use, otc - keep out of reach of children, dosage & administration, otc - questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose: Antiseptic
Indications & Usage
Use: For hand washing to decrease bacteria on the skin. Recommended for repeated use.
Warnings
Warnings: Flammable, keep away from fire or flame. For external use only. Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation and redness develop. If condition persists for more than 72 hours consult a doctor.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Dosage & Administration
Directions: Wet hands thoroughly with product and allow to dry without wiping.
Otc - Questions
Questions? 1-323-284-9021 weekdays, 9am to 5pm PST
Ili Hand Sanitizer 8 Fl Oz
MM1:8floz_ILI_Hand_Sanitizer_Label rev 3_Page_1.jpg
Inactive Ingredient
water, isopropyl alcohol, glycerin, methyl gluceth-20, panthenol, tocopheryl acetate, benzalkonium chloride, polysorbate 20, carbomer, sodium benzotriazolyl butylphenol sulfonate, aminomethyl propanol, fragrance
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