Active Ingredient
Alcohol 62% v/v
Hand Sanitizer Gel
FDA Label NDC 69396-137
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Trifecta Pharmaceuticals Usa for the product Hand Sanitizer (NDC 69396-137). 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, directions, keep out of reach of children, inactive ingredients, 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 to decrease bacteria on skin without soap and water
Warnings
- for external use only
- Use with caution if allergic to alcohol.
- Flammable. Keep away from heat or flames.
Do Not Use
Do not Use
- in the eyes
Directions
Put enough product on your palm to cover hands and briskly rub hands together until dry.
Keep Out Of Reach Of Children
For Children under 6 years old, use only under adult supervision
Inactive Ingredients
Aloe barbadensis leaf juice, Acrylates/C10-30 alkyl acrylate crosspolymer, Fragrance, Glycerin, Maltodextrin, Propylene glycol, Tocopheryl acetate, Triethanoamine, water.
Other Information
- Do not store above 105°F
- May discolor some fabrics
- Harmful to wood finishes and plastic
Distributed By:
Trifecta Pharmaceuticals USA®
101 NE Third Avenue, Suite 1500
Ft. Lauderdale, FL. 33301 USA
www.trifecta-pharma.com
1-888-296-9067
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