Active Ingredient(S)
Alcohol 75%
Instant Hand Sanitizer
FDA Label NDC 78294-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Lotus Arts Crafts Limited for the product Instant Hand Sanitizer (NDC 78294-001). 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 active ingredient(s), purpose, use for hand, 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 For Hand
washing to decrease bacteria on the skin ,only when water is not available
Warnings
For external use only. Flammable. Keep away from heat or flame
Do Not Use
Do not get into eyes. If contact occurs ,rinse eyes thoroughly with water
Otc - When Using
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Otc - Stop Use
Imitation and redness develop.
Keep out of reach of children.
If swallowed ,get medical help for contact a Poison Control Center right away.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Directions
Wet hands thoroughly with product and allow to dry without wiping
Other Information
Store below 105° F
Inactive Ingredients
Aqua(water) ,Glycerin, Carbomer, Propylene glycol, Triethanolamine ,Aloe Barbadensis Leaf Extract
Package Label - Principal Display Panel
Package (Package)
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