Active Ingredient
Ethyl Alcohol 62%
Antibacterial Hand Sanitizer Gel
FDA Label NDC 73796-110
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Prostock Llc for the product Antibacterial Hand Sanitizer (NDC 73796-110). 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, when using this product, stop use and ask a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
•For Hand Sanitizing
Warnings
For external use only-hands.
Flammable. Keep away from heat and flame.
When Using This Product
Keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest.
Stop Use And Ask A Doctor If
skin irritation develops.
Keep Out Of Reach Of Children.
If swallowed, get medical help or call a Poison Control Center right away.
Directions
•Wet hands thoroughly with product and allow to dry without wiping.
•For children under 6 age use only under adult supervision.
•Not recommended for infants.
Other Information
•Do not store above 105°F.
•May discolor some fabrics.
Inactive Ingredients
Carborner, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate, Triethanolamine, Water.
Package Labeling: 73796-110-15
Label (Label)
Package Labeling: 73796-110-30
Label2 (Label2)
Package Labeling: 73796-110-60
Label3 (Label3)
* Please review the disclaimer below.
