Active Ingredient(S)
Ethyl Alcohol 75% V/v
Hand Sanitizer Gel
FDA Label NDC 58503-805
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by China Ningbo Shangge Cosmetic Technology Corp. for the product Hand Sanitizer Gel (NDC 58503-805). 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, do not use, otc - when using, otc - stop use, 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
Use
Use on hands to kill bacteria
Warnings
For extemal use only. Flammable, Keep away from heat or flame
Do Not Use
/
Otc - When Using
/
Otc - Stop Use
/
Otc - Keep Out Of Reach Of Children
If swallowed seek medical advice immediately and show this container or label
If irritation or redness develops and lasts more than 72 hours, consult a doctor or seek medical help
Directions
Wet hands thoroughly with product and allow to dry without wiping
Other Information
● Store between59-86°F(15-30°c)
● Avoid freezing and excessive heat above104°F(40°c)
Inactive Ingredients
Carbomer, Glycerol, Triethanolamine, Water
Package Label - Principal Display Panel
Label (Label)
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