Active Ingredient
Ethyl Alcohol 70.00%
Sanitizer Advanced Hand
FDA Label NDC 77449-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Glowbal Citizen Llc for the product Sanitizer Advanced Hand (NDC 77449-001). 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 active ingredient, purpose, uses:, warnings:, when using this product, stop use and ask a 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 baceteria on the skin that colud cause diseases.
Warnings:
Flammable. Keep away from fire or flame. For external use only.
When Using This Product
do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Stop Use And Ask A Doctor
if irritation or rash appears and lasts.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions:
Place enough product in the palm of your hands to thoroughly cover you hands. Rub hands together briskly until product is completely absorbed and hands are dry.
Inactive Ingredients:
Aqua, Glycerin, *CO Glycerin, *CO Humulus Lupulus (Hops) Extract, *Co Lavandula Angustifolia (Lavender) Flower/Leaf/Stem Extract, *CO Calendula Officinalis Flower Extract, *CO Chamomilla Recutita (Matricaria) Flower Extract, *CO Citrus Limon (Lemon) Peel Extract, *CO Camellia Sativus (Cucumber) Seed Extract, *CO Camellia Sinensis Leaf Extract, *CO Pyrus Malus (Apple) Fruit Extract, *CO Spirulina Platensis Extract, Carbomer. *CO Certified Organic
Package Labeling:
Lable (Lable)
* Please review the disclaimer below.
