Dosage & Administration
Do not store above 105 °F
Hand Sanitizer
FDA Label NDC 87269-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ningbo Meidi Cosmetics Co., Ltd. for the product Hand Sanitizer (NDC 87269-002). 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 dosage & administration, inactive ingredient, indications & usage, otc - active ingredient, otc - keep out of reach of children, otc - purpose, warnings, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
aqua，glycerin，propylene glycol，carbomer，triethanolamine，red 33,blue 1,yellow 5
Indications & Usage
Wet hands thoroughly with product and rub until dry without wiping.
Otc - Active Ingredient
ethyl alcohol
Otc - Keep Out Of Reach Of Children
keep out of reach of children
Otc - Purpose
Disinfection
Sterilization
No Rinseing
Warnings
●For external use only.
●Flammable.Keep away from heat and flame.
●Discontinue if skin becomes irritated and ask a doctor.
●Keep out of reach of children.
●In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.
Package Label.Principal Display Panel
Label (Label)
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