Otc - Active Ingredient
Active ingredients: Ethyl Alcohol 70%
Hand Sanitizer Spray
FDA Label NDC 87662-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Lessdotw Co.,ltd. for the product Hand Sanitizer (NDC 87662-101). 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 otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, other safety information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Inactive ingredients: Water, Fragrance, Saccharide Isomerate, Citric Acid, Sodium Citrate, Xylitylglucoside, Anhydroxylitol, Xylitol, Glucose, Aloe Barbadensis Leaf Juice
Otc - Purpose
Purpose: Antiseptic
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.
Indications & Usage
For handwashing to decrease bacteria on the skin. Recommended for repeated use when soap and water are not available
Warnings
Warnings:
For external use only. Hands.
Flammable. Keep away from heat or flame.
Dosage & Administration
Spray on hands and rub thoroughly until dry
Children under 6 years: use under adult supervision
Other Safety Information
Other:
Store below 40°C / 104°F
Avoid freezing and excessive heat
Use Non Alcohol Hand Sanitizer for the refill only.
Shelf life: 3 years (Refer to packaging box for MFG/LoT info)
Otc - Ask Doctor
Stop use and ask a doctor if
irritation or redness develops.
condition persists for more than 72 hours.
Package Label.Principal Display Panel
Hand Sanitizer (Label)
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