Active Ingredient
Ethyl alcohol 72%
Advanced Hand Sanitizer
FDA Label NDC 75311-000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Unisources Group Llc for the product Advanced Hand Sanitizer (NDC 75311-000). 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, do not use, 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
- Hand sanitizer to help reduce bacteria on the skin
- Recommended for repeated use
Warnings
- Flammable, Keep away from fire or flame.
- For external use only.
Do Not Use
- in or near the eyes. in case of contact, flush eyes with water.
Stop Use And Ask A Doctor If
- irritation or rash appears and lasts.
Keep Out Of Reach Of Children.
- If need, get medical help or contact a Poison Control Center.
Directions
- Wet hands thoroughly with enough product and allow to dry without wiping.
- Children under 6 years of age use only under adult supervision when using this product.
Other Information
- Store below 105°F(43 C)
- Surface to wood and plastics.
- May discolor certain fabrics or surfaces
Inactive Ingredients
Water, Glycerin, Aloe barbadensis leaf extract, Carbomer, Tocopheryl Acetate, Triethanolamine.
Package Labeling: 59Ml
Bottle (Bottle)
Package Labeling: 236Ml
Label2 (Label2)
Package Labeling: 295Ml
Bottle3 (Bottle3)
* Please review the disclaimer below.
