Active Ingredients
Ethyl Alcohol 75%
Hand Sanitizer Gel
FDA Label NDC 74046-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dongguan Mingyi Medical Products Co., Ltd. for the product Hand Sanitizer Gel (NDC 74046-001). 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 ingredients, uses, warnings, directions, other information, inactive ingredients, package label - principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Uses
Hand Sanitizer to help reduce bacteria on skin.
Warnings
For external use only.Keep out of reach of children.Children must be supervised if using this product.
Flammable.Keep away from fire or flame.
Avoid contact with eyes.Discontinue use if irritation or redness occurs.If irritation continues for more than 72hrs, please
consult a doctor.
Directions
Place enough in your palm to thoroughly spread on both and rub into the skin until dry.
Children under 6 years of age should be supervised when using this product.
Other Information
store below 160°F.(41℃)
may discolor certain fabrics or surfaces
Inactive Ingredients
Water(Aqua),Carbomer, Glycerol,Propylene Glycol,triethanolamine,Poly(acrylic acid)
Package Label - Principal Display Panel
50 mL Label (Label4)
60 mL Label (Label5)
100 mL Label (Label6)
236 mL Label (Label7)
240 mL Label (Label8)
250 mL Label (Label9)
500 mL Label (Label10)
* Please review the disclaimer below.
