Directions:
Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.
Handzitizer
FDA Label NDC 79536-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Synbionic Evolution, Inc. for the product Handzitizer (NDC 79536-002). 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 directions:, warning, non medicinal ingredients, use, keep out of reach of children, purpose, active ingredient:, handzitizer, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Warning
For external use only. Flammable. Keep away from heat or open flame.
Non Medicinal Ingredients
Purified water USP, Glycerin, Acrylic Acid Copolymer
Use
To help reduce bacteria that potentially can cause disease. For when soap and water are not available.
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away. Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Purpose
Antiseptic, Hand Sanitizer
Active Ingredient:
Alcohol, USP grade. 70% V/V
Handzitizer
Handzitizer (1000L)
* Please review the disclaimer below.
