Otc - Active Ingredient
benzaklonium chloride 0.66%
Mediplus Hand Sanitizer
FDA Label NDC 74713-0001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Gl Pharm Co Ltd for the product Mediplus Hand Sanitizer (NDC 74713-0001). 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 otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, 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
polyoxyethylene lauryl ether, ethanol, purified water
Otc - Purpose
hand sanitizer
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF THE CHILDREN
Indications & Usage
Apply to clean, dry hands. Apply sufficient amount to thoroughly wet all surfaces of hands and fingers. Rub onto hands until dry.
Supervise children in the use of this product.
Warnings
■ Flammable. Keep away from fire or flame.
■ For external use only.
■ Do not use in eyes.
■ lf swallowed, get medical help promptly.
■ Stop use, ask doctor lf irritation occurs.
■ Keep out of reach of children.
Dosage & Administration
for external use only
Package Label.Principal Display Panel
Label (Label)
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