Active Ingredients
Ethyl Alcohol 70%
Defense Zone
FDA Label NDC 13630-0161
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Prime Packaging for the product Defense Zone (NDC 13630-0161). 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 ingredients, purpose, uses, warning, dot not use, when using this product, stop use and ask a doctor, 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
to decrease bacteria on the skin that could cause disease. recommrnded for repeated use
Warning
For external use only
Dot Not Use
Do not use on damaged or broken skin
When Using This Product
Keep away from face to avoid breathing it. Keep out of eyes. rinse with water to remove.
Stop Use And Ask A Doctor
If irritation and redness occurs if condition persistes for more than 72 hours.
Keep Out Of Reach Of Children
If product is swallowed, get medical help or contact a Posion Control Center right away.
Flammable
Avoid fire, flame, heat and smoking. Contents under pressre. do not punture or incinerate. Store at temperatures below 120°F(50°C).
Directions
wet hands thoroughly with product and allow to dry without wiping. for children under 6, use only under adult supervision. not recommended for infants.
Other Information
do not store above 104°F. may discolor some fabrics. harmful to wood finishes and plastics.
Inactive Ingredients
Aloe Barbadensis Leaf Juice,Glycerin,Isopropyl Myristate, Tocopherol,Water.
Questions
Call 1 855-548-4653
Principal Display Label
Principle Display Label (13630 0161 4)
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