Uses
to decrease bacteria on the skin that could cause disease.
recommended for repeated use.
Hand Sanitizer
FDA Label NDC 55469-008
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dongyang Liulu Cosmetics Co.ltd for the product Hand Sanitizer (NDC 55469-008). 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 uses, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, indications & usage, other information, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Warnings
For external use only. Flammable.Keep away from fire or flame
Otc - When Using
keep out of eyes.
ln case of contact with eyes.
flush thoroughly with water.
avoid contact with broken skin .
do not inhale or ingest.
Otc - Stop Use
irritation or redness develops .
condition persists for more than 72 hours.
Otc - Keep Out Of Reach Of Children
If swallowed. get medical help or contact a Poison Control Center right away.
Indications & Usage
Place enough product on hands to cover all surfaces.Rub hands together until dry.Supervise children under 6 years of agewhen using this product to avoid swallowing.
Other Information
Do not store above 105°F
May discolor some fabrics
Harmful to wood finishes and plastics.
Inactive Ingredient
purified water
Otc - Active Ingredient
ALCOHOL 75%
Otc - Purpose
Disinfection
Sterilization
Package Label.Principal Display Panel
Label (Label)
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