Active Ingredient(S)
Benzalkonium Chloride 0.1% v/v. Purpose: Antiseptic
G3tech Hand Sanitizer
FDA Label NDC 79176-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Freshstart Holding Inc for the product G3tech Hand Sanitizer (NDC 79176-001). 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 active ingredient(s), purpose, use, warnings, directions, other information, inactive ingredients, otc - 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
Purpose
Antiseptic, Hand Sanitizer
Use
Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Warnings
For External Use Only.
Directions
- Squeeze a few drops onto palm.
- Rub onto entire area of hands, including backs, wirsts and between fingers until dry.
- No rinsing required.
Other Information
- Store in a cool dry place
- Keep away from direct sunlight
Inactive Ingredients
Aqua,
Glycerin,
Anthemis Nobilis (Chamomile) Flower Water,
Acrylates/C 10-30 Alkyl Acrylate Crosspolymer,
Citric Acid,
Lavandula Angustifolia (Lavender) Oil,
Aloe Barbadensis Leaf Juice,
Hydroxypropyl Methylcellulose,
Curcumin,
Korean Pine Oil
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Package Label - Principal Display Panel
60ml NDC: 79176-001-01
500ml NDC: 79176-001-02
1000ml NDC: 79176-001-03
* Please review the disclaimer below.
