Active Ingredients
Ethyl Alcohol 70%
Instant Hand Sanitizer
FDA Label NDC 73817-100
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by American Screening Llc for the product Instant Hand Sanitizer (NDC 73817-100). 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, purpose, use, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antibacterial
Use
For rinse-free hand sanitizing to remove 99.9% bacteria on skin.
Warnings
Flammable. Keep away from fire or flame. For external use only.
When Using This Product
Do not use in eyes. In case of contact with eyes, rinse with water.
Stop Use And Ask A Doctor If
irritation and redness develop and persist.
Keep Out Of Reach Of Children.
If swallowed, get medical health promptly
Directions
Wet hands thoroughly with product and allow to dry without wiping.
Other Information
Store under 105°F
Inactive Ingredients
Aloe Barbadenisis Leaf, Glycerin, Hydroxypropylcellulose, Vitamin E, Water
Package Label.Principal Display Panel
4 ounces (118 mL) - NDC 00000-000-00
Label-4oz (Label 4oz)
8 ounces (236 mL) - NDC 00000-000-00
Label-8oz (Label 8oz)
16 ounces (437 mL) - NDC 00000-000-00
Label-16oz (Label 16oz)
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