Sanitizer Spray
FDA Label NDC 79396-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bozzano Group for the product Sanitizer (NDC 79396-001). 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 ingredient, purpose, use, warnings, 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
Active Ingredient
Ethyl Alcohol 70%
Purpose
Antiseptic
Use
for hand-washing to decrease bacteria on the skin, and for disinfect objects.
Warnings
Flammable, keep away from fire and flames.
For external use only
When Using This Product
- do not get into eyes.
- if contact occurs, rinse eyes thoroughly with water
Stop Use And Ask A Doctor If
- irritation and redness develop
Keep Out Of Reach Of Children.
if swallowed, get medical help or contact a Poison Control Center right away
Directions
- Wet hands or objects thoroughly with product and allow to dry without wiping.
Other Information
- Store below 105 °F.
- May discolor some fabrics.
Inactive Ingredients:
Water, Glycerin, Fragrance, Tocopheryl Acetate (Vitamin E).
Package Labeling:
Label (Label)
* Please review the disclaimer below.
