Dosage & Administration
Store below 110°F (43°C)
Hand Sanitizer
FDA Label NDC 52692-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangdong Songtaixing Cosmetics Industry Co., Ltd for the product Hand Sanitizer (NDC 52692-001). 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 dosage & administration, inactive ingredient, indications & usage, otc - active ingredient, otc - keep out of reach of children, otc - purpose, warnings, 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
Inactive Ingredient
Water,Glycerol, PEG/PPG-17/6 Copolymer,Carbomer,Triethanolamine,Parfum,Citrus Aurantium Dulcis(Orange) Oil
Indications & Usage
Place enough product in your palm to thoroughly cover your hands.Rub hands together briskly until dry
Otc - Active Ingredient
Ethanol
Otc - Keep Out Of Reach Of Children
keep out of reach of children
Otc - Purpose
Disinfection
Sterilization
No Rinseing
Warnings
Flammable, keep away from fire or flame .
Package Label.Principal Display Panel
Label (Label)
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