Active Ingredient
Ethyl Alcohol 75%
Hand Sanitizer
FDA Label NDC 74763-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Gafle Auto Chemical Co., Ltd. for the product Hand Sanitizer (NDC 74763-001). 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, purpose, uses, warnings, when using this product, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Uses
Hand Sanitizer to help reduce bacteria on skin
Warnings
Flammable. Keep away from fire or flame. For external use only.
When Using This Product
do not use in near the eyes. In case of contact, rinse eye thoroughly with water. Stop use and ask doctor if irritation or rash appears and lasts. Keep out of reach for children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry.
Children under 6 years of age should be supervised when using this product.
Other Information
Store below 106° F.(41C°)
Inactive Ingredients
Purified water, Glycerin, Triethanolamine, Carbomer, Vitamin E
Package Label - Principal Display Panel
1 (Fda500ml)
2 (Fda1000ml)
59ml (Fda59ml)
250ml (Fda250ml)
100ml (Fda100ml)
* Please review the disclaimer below.
