Active Ingredients
0.13% Benzylkonium Chloride
Freshorize
FDA Label NDC 52305-300
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Freshorize, Ltd. for the product Freshorize (NDC 52305-300). 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 ingredients, indications & usage, warnings, display of package label., keep out of reach of children, purpose, dosage & administration, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Indications & Usage
Requires no water or towels. Apply small amount to hands and rub lightly until dry.
Warnings
Safety: Avoid contact with Eyes, should this occur rinse immediately with clean warm water.Caution: Use on hands only.
Display Of Package Label.
Picture of Package Label
Freshorize Non-alc Label (Freshorize Alc Free Label)
Keep Out Of Reach Of Children
Keep out of reach of children
Purpose
Kills 99.9% Bacteria
Dosage & Administration
Requires no water or towels.
Apply small amount to hands and rub lightly until dry.
Inactive Ingredient
Aqua, Polysorbate 40, Aloe Barbadensis, Parfum
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