Defense Hand Sanitizer Liquid
FDA Label NDC 80579-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Walla Walla Environmental, Inc. for the product Defense Hand Sanitizer (NDC 80579-001). 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 ingredients, purpose, use[s]:, warnings:, do not use, when using this product, stop use and ask a doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
Isopropyl Alcohol 75% v/v
Purpose
Antiseptic
Use[S]:
Use as hand sanitizer to reduce bacteria on skin when soap and water are not available, recommended for repeated use
Warnings:
For external use only.
Flammable. Keep away from fire or flame.
Do Not Use
- On children less than 2 years of age.
- On open skin wounds.
When Using This Product
keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop Use And Ask A Doctor
if irritation or rash occurs. These may be signs of a serious condition.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions:
• Place enough product on hands to cover all surfaces. Rub hands together until dry,
• Supervise children using this product to avoid swallowing.
Other Information
- Store between 15-30C [50-86F]
- Avoid freezing and excessive heat above 40C [104F]
Inactive Ingredients:
water, hydrogen peroxide, lemongrass oil, glycerin.
Package Labeling:
Box3 (Box3)
* Please review the disclaimer below.
