Active Ingredient(S)
Ethyl Alcohol 75% v/v.
Hand Sanitizer
FDA Label NDC 58503-801
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 (NDC 58503-801). 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
Antimicrobial
Use
for handwashing to decrease bacteria on the skin
recommended for repeated use
Warnings
For external use only
Flammable, keep away from heat and flame.
Do Not Use
Do not use in the eyes In case of contact rinse eyes thoroughly with wafer
Otc - When Using
/
Otc - Stop Use
Stop use, and ask a doctor if irritation and redness develop and persistfor more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed. get medical help or contact a Poison Control Center right away.
Directions
wet hands thoroughly with product briskly rub hands together until dry
supervise children under 6 years in the use of this product
Other Information
store at 20°C to 25°C(68° to 77°F)
may discolor certain fabrics
Inactive Ingredients
Water, Glycerin, Carbomer, Aloe Vera, Trithanolamine, Vitamine E
Package Label - Principal Display Panel
1 (1)
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