Active Ingredient
Benzalkonium Chloride 0.12%
Zogics Foam Hand Sanitizer Liquid
FDA Label NDC 72202-282
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zogics, Llc for the product Zogics Foam Hand Sanitizer (NDC 72202-282). 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, do not use, when using this product, stop use and ask a doctor if, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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.
Warnings
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 Doctor If
irritation and redness develop. If condition persists for more that 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 whtn using this product.
Other Information
Store in a cook, dry place.
Inactive Ingredients
Water, Aloe Barbadensis Leaf Juice, Polysorbate 20, Glycerin, Potassium Sorbate, Fragrance, Citric Acid, Disodium EDTA, Tocopheryl Acetate (Vitamin E).
* Please review the disclaimer below.
