Full Clean Hand Sanitizer
FDA Label NDC 81167-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Luxe Tech Llc for the product Full Clean Hand Sanitizer (NDC 81167-001). 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 drug facts, active ingredient, purpose, use:, warnings:, do not use, stop use and ask a doctor if, keep out of the reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
65% ETHYL ALCOHOL v/v
Purpose
Antimicrobial
Use:
Hand sanitizer to help reduce germs on the skin that can potentially cause disease.
Warnings:
Flammable. Keep away from fire or flame.
Do not inhale or ingest.
Do Not Use
near or in the eyes. In case of contact, flush eyes with water. Avoid contact with broken skin.
Stop Use And Ask A Doctor If
irritation or redness develops and lasts.
Keep Out Of The Reach Of Children.
If swallowed get medical help or contact a poison control center right away.
Directions:
Put enough product in your palm to cover hands completely and rub hands briskly together until dry. Children under 6 years old should be supervised when using this product.
Other Information:
Store below 110°f (43°c). May discolor certain fabrics or surfaces.
Inactive Ingredients
Aqua (Water), Aloe Barbadensis Leaf Extract (Aloe Vera), Hydroxyethyl Cellulose (gelling agent), Triethanolamine (for pH balance).
* Please review the disclaimer below.
