Total Sanitizer Alcohol Free Hand Saniting Foam
FDA Label NDC 80463-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Total Sanitizer, Llc for the product Total Sanitizer Alcohol Free Hand Saniting Foam (NDC 80463-003). 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, uses, warnigns, do not use, when using this product, stop use and ask a doctorif, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Benzalkonium Chloride 0.12%
Purpose
Antiseptic
Uses
- For handwashing to decrease bacteria on the skin.
- After changing diapers.
- After assisting ill persons.
- Before contact with a person under medical care or treatment.
- Recommended for repeat use.
Warnigns
For external use only.
Do Not Use
in the eyes.
When Using This Product
do not get into eyes. If contact occurs. rinse thoroughly with water.
Stop Use And Ask A Doctorif
irritation and redness develop. If condition persists for more than 72 hours consult a doctor.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Wet hands thoroughly with product and allow to dry.
- Children under six years of age should be supervised when using this product.
Other Information
- Store in a cool, dry place.
Inactive Ingredients
Water, Aloe Barbadensis Leaf Juice, Polysorbate 20, Glycerin, Potassium Sorbate, Fragrnace, Citric Acid, Disodium EDTA, Tocopheryl Acetate (Vitamin E).
Package Labeling:
Label3 (Label3)
* Please review the disclaimer below.
