Active Ingredient
Ethyl Alcohol 70%
Hand Sanitizer
FDA Label NDC 75118-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shandong Aoyou Biotechnology Co.,ltd for the product Hand Sanitizer (NDC 75118-002). 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, purpose, uses, warnings, when using this product, otc - stop use, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
to decrease bacteria on the skin that could cause disease . recommended for repeat use
Warnings
For external use only:hands
Flammable, Keep away from fire or flame.
When Using This Product
keep out of eyes.In case of contact with eyes, flush thoroughly with water.avoid
contact with broken skin.do not inhale or ingest
Otc - Stop Use
Stop using and ask a doctor if irritation or redness develops.condition persists for more than 72 hours.
Keep out of reach of children.lf swallowed,get medical help or contact a Poison Control Center right away.
Directions
wet hands thoroughly with product and allow to dry without wiping.for children under 6,use only
under adult supervision. not recommend for infants.
Other Information
do not store above 105°F
may discolor some fabric
harmful to wood finishes and plastic.
Inactive Ingredients
purified water
Package Label - Principal Display Panel
500 mL Label (Label)
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